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Tilburg University
Research for policy
Hegger, Ingrid
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Publication date:2017
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Citation for published version (APA):Hegger, I. (2017). Research for policy: A study on improving the contribution of scientific knowledge to evidence-informed health policy. Gildeprint.
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Research for Policy A
study on improving the contribution of scientific know
ledge to evidence-informed health policy
Ingrid Hegger
Research for PolicyA study on improving the contribution of
scientific knowledge to evidence-informed health policy
Ingrid Hegger
Evidence-informed health policy-making is generally considered as an important approach
for safeguarding public health: governments should take into account the best available
research evidence in health policy-making. Most countries have established a National
Public Health Institute to support their government in essential public health operations by
activities such as health protection, population health assessment and research to produce
evidence for policy-making. However, researchers experience that achieving contributions
to health policy-making appears to be more difficult than one would expect in view of the
institute’s mission. In the body of scientific literature on knowledge utilization, alignment
between researchers and policy-makers is recognized as an important key for enhancing
contributions of scientific knowledge to policy-making.
This thesis describes a study investigating how alignment is achieved and can be improved
in research projects conducted by a National Public Health Institute in commission of
governmental organizations.
Uitnodiging
voor het bijwonen van de openbare verdediging van mijn proefschrift
Research for PolicyA study on improving
the contribution of scientific knowledge to evidence-informed
health policy
op woensdag 6 september 2017 om 16:00 precies in de aula van de
Universiteit van Tilburg,Warandelaan 2 te Tilburg
Aansluitend bent u
van harte welkom opde receptie ter plaatse
Ingrid HeggerSoestdijkseweg Zuid 19
3732 HC De [email protected]
06-38464916
Paranimfen:Thomas Bakker
Esther [email protected]
De aula bevindt zich in het Cobbenhagengebouw,
te bereiken via het Koopmansgebouw. Bij de universiteit is voldoende
parkeergelegenheid. Station Tilburg Universiteit is op
10 minuten loopafstand.https://www.tilburguniversity.edu/nl/
contact/campus-map/
Research for Policy
A study on improving the contribution ofscientific knowledge to evidence-informed health policy
Ingrid Hegger
Colofon
The research for this thesis was supported by the Strategic Research Programme 2011-
2014 of the Dutch National Institute for Public Health and the Environment (RIVM) (project
number S/270206).
The printing was financially supported by Tilburg University and the National Institute for
Public Health and the Environment (RIVM).
ISBN
978-94-6233-673-5
Cover
‘Connections’ by Louise van Terheijden, Tilburg
http://louisevanterheijden.com/
Lay-out
Nicole Nijhuis - Gildeprint, Enschede
Printed by
Gildeprint - Enschede
Copyright ©Ingrid Hegger
All rights reserved. No part of this thesis may be reproduced, stored in a retrieval system or
transmitted in any form by any means without prior permission of the author.
Research for Policy
A study on improving the contribution ofscientific knowledge to evidence-informed health policy
Proefschriftter verkrijging van de graad van doctor aan Tilburg University
op gezag van de rector magnificus, prof.dr. E.H.L. Aarts,
in het openbaar te verdedigen ten overstaan van een
door het college voor promoties aangewezen commissie in de aula van de Universiteit
op woensdag 6 september 2017 om 16.00 uur
door
Ingrid Heggergeboren te ‘s-Gravenhage
Promotiecommissie
Promotores
Prof.dr.ing. J.A.M. van Oers
Prof.dr.ir. A.J. Schuit
Copromotor
Dr. S.W.J. Janssen
Overige leden
Prof.dr. L.A.M. van de Goor
Prof.dr.ir. M.W.J. Jansen
Prof.dr. M.A. van der Steen
Prof.dr. G.P. Westert
Dr. M.P.M. Bekker
Mijn proefschrift draag ik op aanmijn ouders, Hanna en Han, en mijn kinderen, Matthijs, Thomas en Esther.
Contents
Chapter 1 9
Introduction
Chapter 2 29
Thecomplexrelationshipbetweenresearchandhealthpolicy:acomprehensive
overviewoftheoreticalapproaches
Chapter 3 43
Analyzingthecontributionsofagovernment-commissionedresearchproject:
a case study
Chapter 4 75
Enhancingthecontributionsofresearchtohealthcarepolicy-making:
a case study on the Dutch Health Care Performance Report
Chapter 5 91
Contributionsofknowledgeproductstohealthpolicy:acasestudyonthe
Public Health Status and Forecasts Report 2010
Chapter 6 105
ResearchforPolicy(R4P):Developmentofareflectiontoolforresearchers
toimproveknowledgeutilization
Appendix Chapter 6: Research for Policy tool
Chapter 7 151
Discussion and Conclusion
Summary 179
Samenvatting 189
Dankwoord 201
About the author 205
ListofPublications(2011-2017) 207
Chapter 1
Introduction
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Introduction | 11
1Public health for a healthy population
‘The Netherlands healthy and well.’ These words represent the motto of the Ministry of
Health, Welfare and Sport in the Netherlands. On its website, the Ministry declares to have
the ambition of keeping everyone as healthy as possible, as long as possible. Furthermore,
the Ministry intends to support people with a disability and promote societal participation
[1]. This short ministerial mission statement reflects the Dutch implementation of the
worldwide responsibility for all national governments to maintain and enhance the health
of its population as defined in the Universal Declaration of Human Rights [2]. Guaranteeing
public health and maintaining effective health services is a demanding task with many
difficult issues and a major impact on the national budget, asking for wise national and
local policies. In order to ensure the population’s health, governments need to invest in
a health system comprising a public health infrastructure and a well performing health
care system. The World Health Organization (WHO) defined ten Essential Public Health
Operations (EPHOs) for the public health infrastructure to assure detecting, measuring, and
tackling health challenges through population-based measures [3]. The health care system
has to offer health services such as preventive, curative and palliative interventions directed
to individuals or to populations [4]. Many countries have established knowledge institutes
for providing support in these governmental tasks, the so-called National Public Health
Institutes (NPHIs) [5, 6].
Worldwide, NPHIs show a great variety in age, history, size, organization, legal basis,
mandate, autonomy, accountability, and financial resources [6]. Due to these differences, a
strict definition of a NPHI does not exist, but they all have a role in the EPHOs and work on
a number of Core Functions (as defined by the International Association of National Public
Health Institutes). These include activities such as population health assessment, health
protection and research to produce evidence [5,7]. NPHIs provide solicited and unsolicited
advice in all phases of public health policy-making. Their research findings support problem
definition and policy prioritization; they integrate knowledge and scientific evidence for
policy development and implementation; by performing health protection tasks, such
as disease surveillance, outbreak investigation and control, environmental monitoring
and managing environmental accidents, they are also involved in the implementation,
maintenance and supervision of public health policy. Finally, they conduct population health
and health systems assessment for policy evaluation [8].
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12 | Chapter 1
In the Netherlands, the National Institute for Public Health and the Environment (RIVM),
functions as a typical NPHI for already more than a century. RIVM has an important role in
the EPHOs during the entire policy cycle for public health and environmental health. RIVM
conducts research and knowledge synthesis in order to support national and international
governmental organizations in the field of public health, health care, medical products,
food and environmental health. Its operational tasks include population health monitoring,
prevention by vaccination, infectious disease management, and population screening [9].
Most NPHIs are (partly) financed by national government funding, whether or not
supplemented with other financial sources. As part of the Ministry of Health or being an
autonomous governmental organization, NPHIs often have to account to the Minister of
Health in some way. For policy advice issues, these characteristics can result in a position
of the NPHI on the nexus of science and policy, where both scientific quality and policy
relevance are at stake.
Research evidence for health policy-making
In recent years, the interest in contributions of knowledge to health policy in order to
enhance public health has grown, among scientists and policy-makers. Worldwide, these
contributions appear to be often more cumbersome than anticipated [10-15]. For example,
NPHIs produce many high quality public health reports, but effective ways of feeding this
knowledge into health policy are difficult to establish. The issue of how to improve scientific
knowledge contributions to the policy-making process has been the research subject of
an extended scientific field, which yielded an impressing amount of scientific publications
[9, 11, 15-23]. Initially, from 1965 onwards, research focused on innovation diffusion and
technology transfer [20]. From around 1985, the emerging Evidence Based Medicine
domain also resulted in increasing research on knowledge utilization in public health [15,
24, 25]. However, empirical studies on knowledge contributions to health policy describing
real-life situations as experienced by scientists and policy-makers are still limited. To find
ways for breaking down barriers in knowledge utilization, detailed insights are needed into
the processes of knowledge production and interaction between researchers and policy-
makers in everyday practice. In this thesis, we describe our study on how contributions of
knowledge from a NPHI to health policy-making are achieved. We have investigated how
these contributions can be enhanced by focusing on the processes involved in the complex
relationship between research and health policy-making and by taking into account the
continuously changing context of the research process.
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Introduction | 13
1Science, research, knowledge and evidence
In the first part of this introduction, the terms science, research, knowledge and evidence
have already appeared without further clarification. These terms are easily used as synonyms,
but their meaning is different. To clarify the term science we refer to the definition by the
Science Council, UK: ‘Science is the pursuit and application of knowledge and understanding
of the natural and social world following a systematic methodology based on evidence’
[26]. In NPHIs, a significant proportion of the scientists have been educated in natural
sciences, in which a positivist view on science is dominant. From a positivist perspective,
science is considered a rational system creating objective, value-free facts by measuring
and observation. These facts reflect the objective single reality. However, for studying the
dynamics of knowledge utilization in policy-making, this perspective does not offer sufficient
understanding. In this thesis, we used the constructivist perspective that considers reality
not a single truth, but a social construct. In this view, science is considered a dynamic social
institution where norms, ideologies, practices, networks and power play a role [27,28].
Where science is the complete system, research is the systematic methodology to investigate
and explain phenomena. As put forward by Hanney, health research can roughly be divided
into basic, clinical and applied research [15]. Clinical research is basically conducted in a
health care setting outside knowledge institutes. A characteristic of basic research is
that the researchers mainly determine priorities; these research findings will generally
not directly be utilized in policy-making. In applied research, other stakeholders, such as
commissioners, governmental organizations and funding organizations, will generally
also play a part in determining the research agenda. Although one could expect that this
involvement will enhance scientific knowledge utilization, reality shows that this is not a
guarantee for research impact and utilization of the findings [15]. In this thesis, we focus
on applied research as conducted by NPHIs commissioned by governmental organizations.
We now come to knowledge, another broad concept closely related to science and research.
Knowledge encompasses all forms of knowing such as scientific findings, theories, data,
experiences and practical skills [17, 29]. From a constructivist perspective, knowledge is
a social construct depending on individuals and organizations involved and created when
people interpret and process different information, such as research findings, theories
and experiences. In this thesis, the term knowledge refers to scientific knowledge based
on research findings. Other types of knowledge are for example practical knowledge, local
knowledge and lay knowledge, but these are not included in this study [17]. In line with
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14 | Chapter 1
science as dynamic social institution, the interpretation and processing of information into
knowledge is also influenced by social processes [28]. Scientific knowledge is neither solely
determined by scientific facts nor value free, which makes it impossible to draw a sharp
line between scientific knowledge and non-scientific knowledge. This also implies that the
boundary between the systems science and policy is not predetermined and more difficult
to set than is (often implicitly) expected [8, 17, 30]. In Chapter 2, we further explore the
complex relationship between science and policy.
Although in scientific literature the term evidence often refers to evidence from scientific
research [31], evidence for policy-making can be different types of information next to
findings from research and scientific knowledge. As described by Bowen and Zwi, types of
evidence can be ideas, interests and information from politics and economics, anecdotal
evidence, knowledge and expertise of experts as well as lay persons, judgements, history,
analogies, local knowledge and culture (table 1.1) [24, 25]. Following the next explanation on
health policy, we return to the issue of evidence types in the section on evidence-informed
health policy.
Table 1.1 Types of evidence and how they are used in policy making [24]
Type of Evidence InformationandInfluenceonDecision-MakingResearch Empirical evidence from randomized control trials and other trials
AnalyticstudiessuchascohortorcasecontrolstudiesTime series analysesObservations,experiences,andcasereportsQualitativeresearchBeforeandafterstudies
Knowledgeandinformation Resultsofconsultationprocesseswithnetworks/groupsInternetPublisheddocuments/reports(includingpolicyevaluationsandstatisticalanalyses)
Ideas and interests Opinion and view- “expert knowledge” of individuals, groups, networks (shaped by pas personal and professional experiences, beliefs, values, skills)
Politics InformationrelevanttotheagendaofgovernmentOpportunityCrises
Economics FinanceandresourceimplicationsCosteffectivenessorotherformsofeconomicevaluationOpportunity cost
BowenS,ZwiAB(2005)Pathwaysto“Evidence-Informed”PolicyandPractice:AFrameworkforAction.PLOSMedicine2(7):e166.https://doi.org/10.1371/journal.pmed.0020166http://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.0020166
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Introduction | 15
1Policy, policy-makers, health policy and the policy process
In this part of the introduction, we explain how we interpret the concepts public policy,
policy-makers, health policy and the policy process.
In general, policy is a very broad concept related to the rational control and governance of
society; we focus on public policy made by government and governmental organizations as a
guide to action and for making choices on goals in a specified area and allocating resources
and capacities to achieve these goals in a specified timeframe [32, 33]. The goals of public
policy are inherently related to public interest and frequently aim to solve so-called ‘common
problems’ that comprise the conflict between public and private interest [34]. The term
policy-makers is used when we refer to the professionals of government / governmental
organizations, who develop policies, often under the authority of a political official [35].
In the context of this thesis, we limit health policy to public policy made by the Ministry of
Health or governmental organizations on an national level with the aim to impact positively
on population health and including both health care policy and public health policy [32].
Agenda setting
Policy formulation
Decision making
Policy implementation
Policy evaluation
Figure 1.1 Policy cycle
Public policy is established in very complex processes for which several different theories
exist nowadays [35, 36]. As Sabatier described, ‘in the process of public policy-making,
problems are and brought to government for solution; governmental institutions formulate
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16 | Chapter 1
alternatives and select policy solutions; and those solutions get implemented, evaluated and
revised’ [36]. The policy-making process is often represented as the policy cycle that includes
the steps agenda setting, policy formulation, decision making, policy implementation and
policy evaluation in a logical, rational sequence.
It should be noted that although the above presented straightforward and rational policy-
cycle provides a helpful overview, this model rather reflects the ideal policy-making process
[34]. In the complex reality of policy-making, the stages are linked but ideas, interests, actors
and value interact in a non-linear fashion [34]. As already recognized by Lindblom (1959),
policy-making has a complex and incremental nature, which he characterized as ‘muddling
through’ [37]. By taking incremental steps, policy-makers can manage the extremely complex
set of interacting elements that is involved in the policy-making process and avoid mistakes.
These characteristic elements include the involvement of many different actors with
different interests, the long lead-time to come from agenda setting to policy evaluation, the
simultaneous action on the same policy issue by different programs at different government
levels, the influence of very technical disputes and the determining role of power elements,
such as interests, money and authoritative coercion [36].
The complex reality of policy-making is important for understanding the use of scientific
knowledge in policy-making, where information, knowledge and evidence have a specific
role. In the political context, the interpretation of information is more powerful for
attaining political goals than the correctness of information, as explained by Stone [34].
For policy-makers, it is crucial to put efforts in strategically controlling the interpretation
of information. Some practices that could be regarded questionable in a scientific context
can be important tools of political strategy, such as selecting the most wanted information,
ignoring information, delaying publication of information and rephrasing information.
Framing of information in a narrative is an important tool for creating the necessity of a
proposed policy; a method that has a different logic than the linear scientific description of
a problem, its cause and solution.
Another relevant characteristic of policy-making is the role of numbers. To attain political
urgency for a problem, the best thing is to assign a number to it, making measuring and
monitoring ambiguous activities in a policy-making context [34]. Findings from measuring or
monitoring will influence the perception of a problem: does the problem (really) exist and to
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Introduction | 17
1whatextent?Fromapoliticalpointofview,theoutcomecouldbeundesirable.Measuring
and monitoring can reveal (new) problems, which is not always politically opportune since
identification of a problem always raises the question of who has to account for it or even
who is to blame for it. This policy-making logic may conflict with the logic pursued by
scientists, who operate on the principle of accepting research findings as they are.
In next chapters, we will often refer to the complexity of the policy-making process and the
consequences for enhancing knowledge contributions.
From evidence-based medicine to evidence-informed health policy
Medicine and health policy-making are naturally closely related worlds influencing each
other. Evidence-informed health policy is a concept coming from Evidence Based Medicine
(EBM) that gained influence by the end of the 20th century [20]. EBM is ‘the conscientious,
explicit, and judicious use of current best evidence in making decisions about the care
of individual patients’ and integrates ‘the best external evidence with individual clinical
expertise and patients’ choice’ [31]. In this context, the best external evidence is considered
to be ‘clinical evidence from systematic research’ such as randomized controlled trials
(RCTs) [31]. EBM implies that the best clinical decisions need three types of knowledge:
research evidence, clinical experience and the patient’s preferences. In line with EBM, the
idea of evidence-based health policy (EBHP) came to the forefront over the past decade
as an important way to improve health systems performance worldwide [38]. In the EBHP
concept, robust research evidence should have an important role as basis for making and
justifying political choices. However, the problems in public health and health systems, such
as health inequalities or lifestyle consequences, are complex, though and persistent; they
are so-called ‘wicked problems’ Wicked problems are difficult to understand and describe,
since they have many causes, uncertainties and levels. They cannot be solved in a finite time-
period by applying straightforward approaches such as an RCT. Many possible outcomes of
a wicked problem exist and the desirability of an outcome depends on values and interests
making the concept of EBHP a wicked problem in turn [21, 39-41].
As we described above, health policy-makers have nevertheless to address these wicked
problems in an often unpredictable and rapidly changing political reality. They have to take
into account many different conflicting interests and next to scientific knowledge, other
knowledge types and considerations influence the policy decision as visualized by Armstrong
et al (see figure 1.2) [13, 24, 33].
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18 | Chapter 1
Know the place of evidence.
Rebecca Armstrong et al. J Public Health 2006;28:168-172
© The Author 2006, Published by Oxford University Press on behalf of Faculty of Public Health. All rights reserved.
Figure 1.2 Know the place of evidence; Armstrong et al (2006) [13]
Putting the role of research evidence in policy-making into perspective clarifies why the
term evidence-informed policy-making (EIPM) is nowadays preferred instead of the term
evidence-based policy-making [40]. Evidence-based could unjustly suggest that policy
decisions should be largely determined by research evidence preferably from RCTs [13,
24, 42]. According to Oxman et al, evidence-informed health policy-making is ‘an approach
to policy decisions that aims to ensure that decision making is well-informed by the best
available research evidence’ [42].
Role of national public health institutes in evidence-informed health policy
To act in accordance with the EIPM concept, policy-makers have to be able to find and
appraise research evidence and acknowledge its possible limitations [42]. NPHIs have
the task to produce knowledge based on research evidence in order to make research
evidence readily available for use in policy-making. Graham et al describe primary scientific
information as first-generation knowledge that is ‘in its natural state and largely unrefined,
like diamonds in the rough’ [29]. Next to first-generation knowledge, they also distinguish
second- and third-generation knowledge. Second-generation knowledge is created by using
systematic, reproducible methods to identify, appraise and synthesize relevant scientific
information into knowledge products such as systematic reviews [29]. For policy-makers, it
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Introduction | 19
1is practically an impossible, time-consuming task if they have to turn to first-generation and
second-generation knowledge (of variable quality) outside their own expertise field. The
NPHI weighs and translates relevant information for the purpose of policy-making and the
knowledge is often presented in a way that specifically meets the needs of the users, such
as tools, websites, infographics, reports or other knowledge products. These knowledge
products represent third-generation knowledge and aim at improving knowledge utilization.
Third-generation knowledge could also intend to influence the behavior of stakeholders by
providing decision tools, guidelines or recommendations [29].
We now reach the point where the inherent tension between usefulness of knowledge
in policy-making and the border between science and policy-making emerges. The more
a knowledge product contains political sensitive findings and recommendations on how
to translate the knowledge into action, the more it comes close to policy-making. As we
explained before, knowledge and research findings have a complex role in policy-making
determined by the actual political context. Such a close-to-policy advice could very well
meet the policy-maker’s need if in line with the actual political view, but could just as well
give rise to concerns about political interference by the NPHI, particularly in case it does
not fit in. The NPHI’s role depends on its legal position, authority and distance to the policy-
making process and its staff has to be aware of their role. A NPHI being part of the Ministry
of Health has to act in a different way than an independent agency not accountable to
the Ministry. Researchers should know what the respective roles are of their institute and
the government department, what their own role should be, how to handle uncertainty
in expertise and how to interact with the policy-makers involved, for example by installing
advisory committees for commissioned research. In order to prevent troubling situations,
NPHIs researchers should also be aware of possible barriers in research utilization that
may relate to expectations placed at the start of the research, the (in)effective transfer of
research findings and the acceptance and interpretation of research findings by individual
policy-makers [11]. They have to negotiate the boundary of their advice by finding the
right balance in wording, format and presentation [43]. This also implies that achieving
optimal knowledge utilization requires a two-way process that includes the policy-makers’
involvement as well [25]. Joint efforts will create knowledge products representing a
serviceable truth, a concept defined by Jasanoff, which means ‘a state of knowledge that
satisfies tests of scientific acceptability and supports reasoned decision making, but also
assures those exposed to risk that their interests have not been sacrificed on the altar of an
impossible scientific certainty’ [44].
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20 | Chapter 1
For researchers at NPHIs, it is very satisfactory when contributions of knowledge to policy-
making are smoothly attained and become clearly visible, specifically when the outside
world recognizes the role of knowledge as basis for the policy choices. However, even
contributions of carefully balanced, third-generation knowledge to policy-making often
appear not to be that straightforward raising the question of what researchers can do to
enhance contributions.
When we consider the differences in the role of information, knowledge, numbers and
measurements in the policy-making context compared to the scientific context and the
need to address wicked problems, the complexity of providing relevant research evidence
for policy-making emerges. In fact, researchers and policy-makers have to align the political
context and the scientific findings [25, 28]. According to Kok and Schuit (2012), the term
alignment, a state of being aligned, ‘emphasizes that accommodation can take place on
the side of research and/or on the side of action, instead of a one-way research to action
dynamic’ [28]. In our study, the side of action was the policy-making context of the Ministry
of Health. We consider alignment as a state in which all actors involved consider the
knowledge products acceptably balanced to the policy-making needs. This balance can
be reached after deliberately bringing together the research context and political context
and by accommodation on either side. Alignment increases the likelihood that beneficial
contributions to health policy can be obtained [28]. Kok and Schuit (2012) propose to call
the specific anticipatory efforts to enhance the contributions to policy-making alignment
efforts [28]. In our study, we also distinguish alignment areas, meaning subject areas where
alignment efforts may focus on.
Despite the large reservoir of scientific literature on the policy-making process, the role of
knowledge in policy-making and knowledge utilization, it remains difficult to identify what
researchers (and policy-makers) can do to enhance contributions. In this study, we intended
to gain knowledge that affords us a glance behind the scenes of this problem. In the specific
context of an NPHI producing knowledge for policy advice in commission of and sponsored
by the government, we investigated contributions of knowledge produced by RIVM to
national health policy-making in the Netherlands.
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Introduction | 21
1Aim of the study
The aim of our study was to acquire insights in how knowledge institutes such as NPHIs
can enhance the contributions to evidence-informed health policy of knowledge produced
in commission of governmental organizations. To investigate this issue, we formulated the
following research questions:
1. What alignment areas are important for enhancing the contributions to health policy
of government commissioned research commissioned by National Public Health
Institutes?
2. Based on the empirical findings gained in this study, what is a practical approach to
enhance knowledge contributions from NPHIs to evidence-informed health policy-
makingatnationallevel?
These research questions rendered specific objectives for this study:
• To map in detail the process of three RIVM projects, the alignment efforts in the
projects and the projects’ contributions to health policy-making at national level;
• To identify the most decisive alignment areas for knowledge contributions to
health policy-making;
• To prepare and evaluate a draft tool based on the theoretical framework and
empirical findings for supporting researchers in alignment.
Study design and outline of the thesis
Foransweringexploratoryquestionssuchas“Whyisavailableknowledge(not)used?”or
“Whatfactorsplayaroleinknowledgeutilization?”qualitativeresearchisoftenseenasthe
most suitable research design, because it pays appropriate attention to the contemporary
and contextual conditions in relation to the topic under research. For this study, we choose
an approach that offered insights into the processes of research projects at the level of daily
practice. Therefore, the study-design was organized along the case study methodology [45].
We selected three cases of research projects according to the following criteria:
• The research projects jointly cover the scope of the RIVM health domain, i.e. public
health, health care and health products, such as medicines, medical devices and
consumer products;
• From the commissioning organization’s perspective, the research projects deal
with sensitive policy issues;
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22 | Chapter 1
• The research projects render third generation knowledge products typical for a
NPHI institute;
• The research projects have different status and size
The first case in the multiple case study was a new project commissioned by the Health
Care Inspectorate in the domain of health products. The project Risk Model started in
2007 and was relatively small in terms of budget and number of researchers involved. The
commissioner’s question was to develop a risk-based approach for stratified selection of
high-risk clinical trials. The Inspectorate intended to implement a risk–based selection
of inspection objects and the risk model aimed to facilitate the selection of the high-risk
trials from the large number of clinical trials conducted every year in the Netherlands. As
an inspection tool, the risk model developed had to remain confidential and could not be
published by RIVM. Although the project started as a one-year project, the Inspectorate
continued the commission in following years.
The second case was the development of the Dutch Health Care Performance Report 2010
(DHCPR) during the period 2008-2010. The Dutch Ministry of Health, Welfare and Sport
commissioned this long-term health care performance monitor initially biannually (editions
in 2006, 2008 and 2010). The last edition was published in 2014, four years after the 2010
edition. The DHCPR had the aim to contribute to strategic health care policy-making, but
was not officially embedded in the policy cycle of the Ministry. Both team and budget were
substantial and many stakeholders outside RIVM were involved. The DHCPR was considered
one of the RIVM flagship-products in the health care domain and was sent to parliament for
informing the members of parliament.
The third case was the production of the Public Health Status Forecasting Report 2010
(PHSF). The PHSF is a major flagship-product and is officially embedded in the policy cycle
by law. The Directorate Public Health of the Ministry of Health, Welfare and Sport acts as
commissioner, but the intended users are all policy-makers of the Ministry. RIVM produces
an edition of the PHSF report every 4 years since 1993. The project team is extended and
cooperates with several other research institutes. The PHSF provides the policy themes for
the legally obliged National Health Memorandum, which is published every four years by
the Minister of Health.
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Introduction | 23
1For analyzing the data collected in the case studies, the Contribution Mapping approach
developed by Kok and Schuit offered a useful model and method to analyze the processes
[28]. Contribution Mapping conceptualizes the utilization and impact of knowledge through
so-called contributions, which are activities that enable the conversion of knowledge into a
component of policies and practices or in innovation. This concept reflects that knowledge
conversion into policy-making can take many, even very subtle, shapes and forms, already
during the research process. For the realization of meaningful contributions, Kok and Schuit
consider specific actions, called alignment efforts, essential to attune research and use. The
qualitative nature of the method and detailed analysis provided in depth understanding of
the alignment processes (or lack of alignment) in research projects and the contributions of
the created knowledge to health policy-making.
In Chapter 2, we provide a concise overview of the theoretical background for the complex
relationship between research and health policy. It describes an influential typology of
knowledge use and successive theoretical models on knowledge utilization [11, 46].
Chapter 3 describes the case study ‘Risk Model’. It contains an outline of Contribution
Mapping as theoretical framework and method for analysis [28]. We analyzed the process
of an RIVM project in which risk ranking models for clinical trials were developed in co-
creation with and in commission of the Health Care Inspectorate. This case study provided
information on important categories of alignment efforts.
In a second case study (Chapter 4), we analyzed the developmental process of the Dutch
Health Care Performance Report 2010 (DHCPR 2010). The DHCPR monitors health care
performance in the Netherlands by using indicators for quality, accessibility and affordability.
This study focused specifically on the process at project level of RIVM researchers and
policy-makers of the Ministry of Health. The study revealed several areas where alignment
is relevant for enhancing the contributions of future reports.
Chapter 5 describes the case study Public Health Status and Forecast Report 2010 (PHSF
2010). The PHSF integrates research data and identifies future trends in public health in the
Netherlands. Since the report has a formalized position in the national public-health-policy
cycle and policy-makers at the Ministry of Health, Welfare and Sport are considered its key
users, PHSF is considered an example of successful boundary work in literature. This study
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24 | Chapter 1
revealed insights on alignment issues in projects that already include several alignment
efforts.
In Chapter 6, the findings of the three case studies are integrated for identifying the most
decisive areas for alignment. The development of the practical tool Research for Policy tool
(R4P tool), based on the decisive alignment areas and intended for researchers, is described.
The R4P tool is presented as an Annex to this chapter.
In Chapter 7, the study as a whole is discussed including a reflection on the methods applied.
Conclusions are drawn in relation to the initial research questions and are completed with
recommendations on practical follow-up and further research opportunities.
Chapter 2 to 6 have been written as articles for international scientific journals. They can be
read independently from each other. However, this also implies that overlap between these
articles exists in theoretical background on the one hand and that divergences in format and
lay-out occur on the other hand.
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Introduction | 25
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20. Estabrooks CA, Derksen L, Winther C, Lavis JN, Scott SD, Wallin L, Profetto-McGrath J. The intellectual structure and substance of the knowledge utilization field: A longitudinal author co-citation analysis, 1945 to 2004. Implement Sci. 2008(3):49.
21. Keijsers JFEM, Paulussen TGWM, Peters LWH, Fleuren MAH, Lammers F. Better use of knowledge: Information behaviour of national policy makers. (In Dutch: Kennis beter benutten: Informatiegedrag van nationale beleidsmakers). Woerden: NIGZ and TNO; 2005.
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22. Landry R, Amara N, Pablos-Mendes A, Shademani R, Gold I. The knowledge-value chain: A conceptual framework for knowledge translation in health. Bull World Health Organ. 2006;84(8):597-602.
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24. Bowen S, Zwi AB. Pathways to “evidence-informed” policy and practice: a framework for action. PLoS medicine. 2005;2(7):e166.
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26. Science Council United Kingdom. Definition of science. Available from: http://sciencecouncil.org/about-us/our-definition-of-science/. Accessed 15 May 2016.
27. Miller C. Hybrid Management: Boundary Organizations, Science Policy, and Environmental Governance in the Climate Regime. Sci Technol Human Values. 2001;26(4):478-500.
28. Kok MO, Schuit AJ. Contribution mapping: a method for mapping the contribution of research to enhance its impact. Health Res Policy Syst. 2012;10:21.
29. Graham I, Logan J, Harrison M, Straus S, Tetroe J, Caswell W, Robinson N. Lost in knowledge translation:timeforamap?JContinEducHealthProf.2006;26:13-24.
30. Van Egmond S, Bekker M, Bal R, van der Grinten T. Connecting evidence and policy: bringing researchers and policy makers together for effective evidence-based health policy in the Netherlands: a case study. Evid Policy. 2011;7(1):25-39.
31. Sackett DL, Rosenberg W, Gray JA, Haynes RB, Richardson WS. Evidence based medicine: what it is and what it isn’t. BMJ. 1996;312(7023):71-2.
32. De Leeuw E, Clavier C, Breton E. Health policy-why research it and how: health political science. Health Res Policy Syst. 2014;12:55.
33. Smith KE, Katikireddi SV. A glossary of theories for understanding policymaking. J Epidemiol Community Health. 2013; 67(2): 198-202.
34. Stone DA. Policy paradox: The art of political decision making. New York Norton & Company Ltd; 2002.
35. Buse K, Mays N, Walt G. Making Health Policy. 2nd ed. Maidenhead: Mc Graw Hill Open University Press; 2012.
36. Sabatier PA. Theories of the Policy Process. Boulder, CO: Westview Press; 2007.37. Lindblom C. The science of “muddling through”. Publ Admin Rev. 1959;19:79.38. Dobrow MJ, Goel V, Upshur RE. Evidence-based health policy: context and utilisation. Socl Sci
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Utilization, and Integration in Public Health. Annu Rev Public Health. 2009; 30:151-174.40. Lomas J, Brown A. Research and advice giving: a functional view of evidence-informed policy
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43. Halffman W, Hoppe R. Science/policy boundaries: a changing division of labour in Dutch expert policyadvice.In:MaasseS,WeingartP,editors.Democratizationofexpertise?Exploringnovelforms of scientific advice in political decision-making. Dordrecht: Kluwer; 2005. p. 135-152.
44. Jasanoff S. The fifth branch: Science advisers as policymakers: Harvard University Press; 1994.
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Introduction | 27
145. Yin RK. Case Study Research Design and Methods. 4th rev ed. Thousand Oaks: SAGE Publications
Inc; 2008.46. WeissC.Policyresearch:data,ideasorarguments?In:WagnerCHWP,WittrockB,WollmanH,
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Chapter 2
The complex relationship between research and health
policy: a concise overview of theoretical approaches
Submitted for publication
Ingrid Hegger
Lisanne K. Marks
Roland A. Bal
Hans A.M. van Oers
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30 | Chapter 2
Abstract
It often appears difficult to realize the integration of scientific knowledge and research
evidence into health policy; a problem which has been subject of extended scientific research
in social sciences for several decades. This article provides a comprehensive overview of the
different theoretical approaches in the complex relationship between science and policy-
making. It describes successive theoretical models on knowledge utilization to inform
researchers who intend to contribute to health policy about their own position in this
complex constellation.
The influential typology of knowledge use provided by Weiss makes a division between
instrumental, conceptual and symbolic use of knowledge. Positivist, interactive and
constructivist models have been developed to explain actual knowledge use and to identify
barriers and enhancers to improve the knowledge utilization. All models offer some part
of understanding about what is going on in the relationship between science and policy.
Although knowledge utilization will remain complex, awareness of the insights from
theoretical models on knowledge utilization in policy-making is a first step and may support
researchers from other scientific disciplines in their efforts to enhance the integration of
evidence into to health policy.
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The complex relationship between research and health policy | 31
2
Introduction
Researchers producing knowledge to support policy-makers have to deal with the complex
relationship between science and health policy. In this paper, we intend to provide these
researchers with a concise overview of the different theoretical approaches to make them
aware of their own position in this relationship and to provide them with insights that can
be of help in cross-disciplinary co-creation processes and in making research relevant and
usable for policy-makers. After all, the awareness of researchers about the sensitive social
issues arising at the nexus of science and policy has been found a decisive factor for the
impact of research in policy-making [1-5].
Different perspectives on knowledge utilization
When aiming at integration of scientific evidence into health policy, researchers should
realize that different perspectives on the use of scientific knowledge in policy-making exist,
depending on the concepts for knowledge production, policy processes and knowledge use
taken as starting points [6].
Knowledge production
In traditional knowledge production, scientists produce knowledge within their own
discipline. Their focus is on science and knowledge in the first place and not necessarily on
the usability of the knowledge produced.
Gibbons et al. described this as ‘Mode 1 knowledge production’ [7]. In the last decades,
Mode 1 knowledge production moved to ‘Mode 2 knowledge production’ in which academics
from different disciplines co-create knowledge together with other partners in a multi-
disciplinary way [7].
Typology of knowledge use
Even if one considers ‘knowledge’ as a clearly defined item, such as an article, it still can
be used in different ways. The most known typology of knowledge use in policy is the one
provided by Weiss that makes a division between research as deliverer of data, ideas and
arguments [8]. This is often described as instrumental, conceptual and symbolic use of
knowledge respectively [9, 10].
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32 | Chapter 2
Instrumental use means that knowledge is considered as technical, objective data and
findings that are utilized in a direct and specific way to solve a particular problem [11].
Instrumental use of knowledge is mostly present in situations in which there is consensus,
both in science and in policy [8].
Research is used in a conceptual way when it delivers ideas that ‘enlighten’ policy-makers
[11]. From the original research, a more or less ‘layman story’ remains which can change
people’s perceptions about problems and can frame those problems for the policy agenda.
This indirect way of use can be observed in cases of high uncertainty about a problem or in
the early stages of a policy discussion [8].
Research influences policy in a symbolic way when it is used as arguments to take an advocacy
position. In this case, politicians and policy-makers may use research data selectively and
strategically to support or strengthen their own position [8]. The knowledge is not used to
inform decision-making, but to justify a pre-chosen position (political use) or to legitimize
(in)action (tactical use) [11]. This type of research use can be observed in conflict situations
[8].
In addition to the typology of Weiss, agenda-setting is sometimes named as a fourth way of
research impact for cases where the research findings itself gives rise to social or political
debate [12]. This however shows large overlap with the conceptual function of knowledge
use.
Modelsforknowledgeutilization
Most people will recognize the different types of knowledge use as described by Weiss from
their own experience. From this typology, several questions naturally follow, such as ‘What
factorsdeterminetheactualknowledgeuseandhowcanweinfluencethe(typeof)use?’.To
handle the complex area of knowledge utilization, successive theoretical models have been
developed which may help to find an answer to these questions. Some of these models—
more specifically the constructivist ones—also challenge the distinction made by Weiss. In
the next sections, we give a brief outline of three approaches: positivist, interactive and
constructivist models.
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The complex relationship between research and health policy | 33
2
Positivist approach models
Positivism is an approach of reality that assumes the existence of a reality driven by natural
laws and mechanisms and of research studying objects without influencing them [13].
Traditional or positivist models on knowledge utilization assume two separate worlds of
science and policy with a strict boundary in between and a one-way relationship [14]. The
positivist perspective regards knowledge as a product for use in policy-making at a certain
point in time. Consequently, these models take the boundaries of both domains as a starting
point to improve knowledge utilization and to look for solutions that try to bridge the so-
called ‘gap’ between these worlds. (Figure 2.1)
Science Policy-making
Figure 2.1 The gap between the world of science and policy-making
A first example of a positivist model is the classic knowledge-driven (or push) model. In this
model, there is a sequence from research to policy utilization with the assumption that
knowledge existence automatically presses to its use [15, 16]. Besides attributes of the
research content, such as complexity and validity, and the type of research, such as method
and domain, high quality research automatically leads to better use by policy makers
according to this model [17].
Another example of a positivist model is the problem solving (or demand pull) model.
Instead of the researchers, the initiative to start research is now shifted to the policy-makers
[17]. Policy-makers identify a particular problem and ask researchers to help formulate
alternatives and solutions to make a policy choice [15].
These rational positivist models mainly focus on the instrumental use of research and
correspond with a technocratic approach to policy-making where decisions unfold through
different sequential stages as part of a policy cycle. (Figure 2.2)
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34 | Chapter 2
Agenda setting
Policy formulation
Decision making
Policy implementation
Policy evaluation
Figure 2.2 Policy cycle
After identifying the problem (agenda setting), policy-makers gather and consider data on
all possible solutions or alternatives relevant for the public interest (policy formulation).
Thereafter, they select a solution depending on predefined goals (decision making). After
the solution has been put into practice (policy implementation), the results are monitored
(policy evaluation) and adjusted when necessary [18]. Assuming that research evidence
easily finds its way to policy-makers and offers ‘neutral’ and ‘objective’ facts, this rational
policy cycle also reflects the different possible roles for research that offers objective and
value-free facts.
However, this model of a one-way policy cycle has been criticized for not corresponding with
the complex and incremental nature of policy-making including many different stakeholders
with their own interests and preferences [19]. In an incremental model of policy-making,
research has a weaker contribution and in comparison with the rational policy cycle,
symbolic use of research is more likely.
Furthermore, the rational science-policy models have been criticized for not attaching much
importance to interaction between producers and users of knowledge and not taking into
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The complex relationship between research and health policy | 35
2
account the organizational and social contexts that may influence the uptake and production
of research. The science-policy model that researchers have (often implicitly) in their mind is
often the rational model. It may be helpful for them to learn about alternative models and
the implications of these models for their own work if taken as a starting point.
Interactive approach models
In response to the drawbacks of the rational models, interactive models of science-
policy relations pay extra attention to context, communication and interaction between
researchers and policy-makers. ‘Socio-organizational explanations’ of knowledge utilization
include organizational interest explanations, ‘two communities’ explanations and interaction
explanations [20]. According to the organizational interest explanation, researchers have to
pay specific attention to the knowledge users’ needs, which depend on their policy domain
or organization. In these models, knowledge use increases when policy-makers consider the
research findings relevant, credible, timely and fitting in with their needs [21].
A model that gained a lot of influence is the ‘two communities’ model [10, 22, 23]. This
model explains the lack of research use by policy-makers as a consequence of a cultural gap
in norms and values between science and policy; both researchers and policy-makers have
their own language and different ways of communication.
Although maybe difficult to achieve, effective interaction to better understand each
other’s worlds is a starting point for increasing the use of research by policy-makers
[22]. The ‘linkage and exchange’ model extended this view by focusing on the broader
institutional and political context and acknowledges both research and policy-making to
be ‘processes’ [23, 24]. Consequently, the use of research by policy-makers is higher when
the research supports an existing policy or corresponds with the ideological environment,
values or interest [10]. In this perspective, adaptation from both researchers and policy-
makers, is necessary to increase research use [9]. For instance, researchers can invest in
the presentation of the research (more readable and understandable) and present specific
(policy) recommendations. At the same time, users can try to influence the topics on the
research agenda in order to get research outcomes that fit with their needs [17].
The interaction model further bridges the gap between the ‘two communities’ by considering
the process of knowledge use as a disorderly and iterative set of interactions between the
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36 | Chapter 2
users and researchers [16, 21]. Relationships between researchers and policy-makers at
different stages of the research process (from formulation to interpretation) have priority
in this model and more investment in different types of linkage mechanisms result in higher
use of research [21]. To analyze knowledge utilization in local policy-making, De Goede et
al. for example developed a model that consists of a policy network and a research network
and identified four categories of barriers in knowledge utilization: expectation, transfer,
acceptance and interpretation [17]. (Figure 2.3) In their model, both networks may overlap
when, for example, policy-makers get involved into the research process by formulating
research questions or researchers in the policy process by communicating or presenting
their results.
Barriers:Expectation, Transfer, Acceptance, Interpretation
Policy network Research network
Research Use
Context
Figure 2.3 Interaction model de Goede [17]
Constructivist approach models
Following the line of knowledge utilization typology via successive models to the current view
that interaction between researchers and policy-makers is a precondition for knowledge
utilization in policy-making, the question is how to design this interaction in order to reach
optimal knowledge utilization. The interaction and network models already show a growing
awareness of the importance of interaction and context. However, these models still assume
an a priori separation of science and policy domains and search for tools and structures to
bridge differences, but the demarcation between science and policy-making is often not
predetermined and as sharp as supposed [1].
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The complex relationship between research and health policy | 37
2
Another way to look at knowledge utilization is the constructivist view that emphasizes the
co-construction of knowledge in a social process and considers boundaries between research
and policy as the outcome of negotiation processes between researchers and policy-makers
[1, 25, 26]. The idea of separate worlds is replaced by the concept of ‘hybrids’ where policy-
makers and researchers co-create knowledge in mutual interaction. In this view, science is
not value-free and only producing facts but is, instead, another social institution with its own
social norms and practices and no conclusive boundaries. In the constructivist perspective,
the notion of knowledge use is problematized, as the positions of producer and user of
knowledge are seen as intertwined.
A constructivist way to look at the relationship between science and policy is represented by
the concept of ‘boundary work’ conducted by scientists and policy makers. Boundary work
is about work done by actors to demarcate science from non-science. Although people use
the concept ‘science’ easily in everyday life, it is in fact impossible to demarcate science in
an unambiguous way. To handle this problem, Gieryn formulated the concept of boundary
work that has to be understood as ‘creating a social boundary that distinguishes science
from intellectual activities that are non-science’ [27]. By conducting boundary work, both
researchers and policy-makers negotiate the boundary between science and policy-making,
where science may come close to policy-making, but not too close [28].
Successful co-creation of knowledge heavily depends on the way the co-creation process
is organized. In this respect, organizations located on the boundary between science and
politics having characteristics of both domains and involving both scientists and policy-
makers in knowledge production, play an important role and are sometimes described as
boundary organizations [29]. Although the boundary between science and policy-making
will continuously be the subject of discussion within such a boundary organization, a stable
boundary can be presented to the outside world.
To provide a further understanding of the interaction between research and policy practices
in boundary organizations, the concepts of frontstage and backstage work by Goffman
(1990) are very helpful [25, 28, 30]. Backstage work stands for the invisible (to outsiders)
coordination process behind the scenes in a knowledge producing process and includes
the knowledge development and learning processes that (invisibly for outsiders) take
place in interaction between the user (policy-maker) and producer (researcher). It is the
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38 | Chapter 2
negotiation process and the search for consensus backstage, including informal contacts
between researchers and policy-makers, that creates trust and makes knowledge (products)
‘acceptable’ at the frontstage [25].
Frontstage work can be described as the way policy-makers and researchers show their
work and work processes to the public [25]. At the frontstage, they present a clear division
of labour and their separated responsibilities. Here, science and policy are seen as two
separate domains with their own tasks; science is depicted as objective and neutral to be
used for politics to make decisions. This image fits the rational and positivist view of policy-
making and science, which is often still a prevalent way to describe the relation between
science and policy. It is at the frontstage where the research (process) gains external
legitimacy and accountability (as being ‘evidence based’), but it is at the backstage where
knowledge utilization is determined. (Figure 2.4)
Knowledge product
Governmental organization
Knowledge production
Research Institute
Front Stage Back Stage
Figure 2.4 Backstage and Front Stage in Knowledge Production
To clarify the constructivist approach, we provide an example.
Commissioned by the Ministry of Health, a public health institute conducts a research on
the implications of nanomaterial use for human health. For the integration of their findings,
they initiate an advisory group in which experts from local health services and national
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The complex relationship between research and health policy | 39
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policy-makers participate. Both researchers and experts feel the need to include policy
recommendations in the final report. However, it becomes clear that some recommendations
are politically controversial and unacceptable for the policy-makers who argue that proposing
political solutions is their job. The questioned policy recommendations would undermine
the acceptance of the report by the Ministry. After exciting negotiations, the group agrees
on reformulated recommendations that maintain the research findings but leave room for
an adequate political response by the Ministry. The director of the public health institute
officially presents the final report to the Minister in presence of the press.
Putting theory into practice
The theoretical models described so far in this article provide useful insights into the
complexity of the science- policy relation, but do not offer many practical leads yet to apply
at the level of research projects. To fill this gap, researchers have to find approaches that
fit their needs while taking into account the theoretical insights into knowledge utilization.
Different theoretical approaches resulted in different practices to improve knowledge
utilization. Knowledge translation including activities as research priority setting, knowledge
distribution and evaluation of uptake is a commonly-used positivist approach [31]. From
the interaction perspective, knowledge brokers linking researchers and knowledge users
act as valuable intermediates to bridge the gap between the two worlds. Furthermore, a
constructivist approach taking into account the complexity of the knowledge production
process offers clear understanding of how to improve alignment between researchers
and knowledge users. For example, Kok and Schuit developed the Contribution Mapping
approach for monitoring research projects [20]. This approach based on constructivism
brings up the moments and areas where specific alignment between knowledge producers
and knowledge users may improve research contributions to policy and practice [3, 4].
Conclusion
In this paper, we provided an overview of theoretical models for knowledge utilization in
health policy-making. All models offer some part of understanding about what is going on in
the relationship between science and policy and it is up to researchers to take advantage of
these models and concepts in aligning with policy-makers.
By acknowledging the complexity of knowledge production as a social process and the need
for intensive interaction with potential users during a research process, a difficult task is
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40 | Chapter 2
added to the responsibilities of researchers. In everyday work, they probably will need to
put flesh on the theoretical concepts described above.
The first step is to become aware of the complexity of science-policy interactions and
the possible ways to approach this complexity. Perhaps, alignment may seem an obvious
precondition to achieve contributions, but in fact it often proves to be very difficult to
achieve [3-5, 17, 32].
The next step that researchers can take to enhance the contributions of their work is to
evaluate their research processes in a structured way and to identify areas for improving
alignment with policy-makers. This takes time and capacity, but renders valuable input
for future projects. In this process, researchers should not hesitate to question their own
normative position and to reflect on the limits of scientific knowledge. As Jasanoff argued,
it is important to take a humble position and to recognize that other information might also
be highly relevant for taking a well-informed and just decision in policy-making [33].
Finally, we advise researchers to take time for regular reflection on their research processes
to stay aware of their role in knowledge utilization and to develop routines for enhancing
the contributions of their work. Like many good habits, this asks for self-discipline, but may
yield much profit.
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The complex relationship between research and health policy | 41
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References1. Wehrens R. Beyond two communities -from research utilization and knowledge translation to
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invloed van adviezen van de Gezondheidsraad. Den Haag: Gezondheidsraad, 2002.3. Hegger I, Janssen SWJ, Keijsers JFEM, Schuit AJ, van Oers, HAM. Analyzing the contributions of
a government-commissioned research project: a case study. Health Res Policy Syst. 2014; 12(1): 8.
4. Hegger I, Marks LK, Janssen SWJ, Schuit AJ, van Oers HAM. Enhancing the contribution of research to health care policy-making: a case study of the Dutch Health Care Performance Report. J Health Serv Res Policy. 2016; 21(1): 29-35.
5. Hegger I, Kok MO, Janssen SWJ, Schuit AJ, van Oers HAM. Contributions of knowledge products to health policy: a case study on the Public Health Status and Forecasts Report 2010. Eur JPublic Health. 2016; 26(6): 922-927.
6. Sedlačko M, Staroňová K. An Overview of Discourses on Knowledge in Policy: ThinkingKnowledge, Policy and Conflict Together. Cent Eur J Public Health. 2016; 9(2): 10-31.
7. Gibbons M, Limoges C, Nowotny H, Schwartzman S, Scott P, Trow M. The new production of knowledge: the dynamics of science and research in contemporary societies. London: Sage; 1994.
8. WeissC.Policyresearch:data,ideasorarguments?In:WagnerCHWP,WittrockB,WollmanH,editors. Social Sciences and modern states. Cambridge: Cambridge University Press; 1991. P. 307–332
9. Amara N, Ouimet M, Landry R. New evidence on instrumental, conceptual, and symbolic utilization of university research in government agencies. Science Communication, 2004. 26(1): 75-106.
10. Innvaer S, Vist G, Trommald M, Oxman A. Health policy-makers’ perceptions of their use of evidence: a systematic review. J Health Serv Res Policy. 2002; 7(4): 239-244.
11. Lavis, JN, Robertson D, Woodside JM, McLeod CB, Abelson J; Knowledge Transfer Study Group. How Can Research Organizations More Effectively Transfer Research Knowledge to Decision Makers? Milbank Q. 2003; 81(2): 221- 248.
12. Bekkers V, Fenger M, Homburg V, Putters K. Doorwerking van strategische beleidsadvisering. Erasmus Universiteit Rotterdam en Universiteit van Tilburg. 2004.
13. Carpiano RM, Daley DM. A guide and glossary on postpositivist theory building for population health. J Epidemiol Community Health. 2006; 60(7):564-570.
14. Gibbons M. Science’s new social contract with society. Nature. 1999. 402(SUPP).15. Weiss CH. The many meanings of research utilization. Public Adm Rev. 1979; 39(5): 426-431.16. Hanney SR, Gonzalez-Block MA, Buxton MJ, Kogan M. The utilisation of health research in policy-
making: concepts, examples and methods of assessment. Health Res Policy Syst. 2003; 1(1): 2.17. deGoedeJ,PuttersK,vanderGrintenT,vanOersHA.Knowledgeinprocess?Exploringbarriers
between epidemiological research and local health policy development. Health Res Policy Syst. 2010; 8(26).
18. Howlett M, Ramesh M. Studying Public Policy: Policy cycles and Policy Subsystems. 1995. Toronto: Oxford University Press.
19. Lindblom CE. The science of “muddling through”. Public Adm Rev. 1959; 19 (2): 79-88.20. Kok MO, Schuit AJ. Contribution mapping: a method for mapping the contribution of research
to enhance its impact. Health Res Policy Syst. 2012; 10: 21.
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42 | Chapter 2
21. Landry R, Lamari M, Amara N. The extent and determinants of the utilization of university research in government agencies. Public Adm Rev. 2003; 63(2): 192-205.
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23. Lomas J. Research and evidence–based decision making. Aust N Z J Public Health. 1997; 21(5): 439-441.
24. Lomas J. Connecting research and policy. Isuma: Can J Policy Research. 2000; 1(1): 140-144.25. Bekker M, van Egmond S, Wehrens R, Putters K, Bal R. Linking research and policy in Dutch
healthcare: infrastructure, innovations and impacts. Evid Policy. 2010; 6(2): 237-253.26. Jasanoff S. The fifth branch: Science advisers as policymakers. Cambridge, MA: Harvard
University Press; 1990.27. Gieryn TF. Boundary-work and the demarcation of science from non-science: Strains and
interests in professional ideologies of scientists. Am Sociol Rev. 1983; 48(6) 781-795.28. Bijker WE, Bal R, Hendriks R. The paradox of scientific authority: the role of scientific advice in
democracies. Cambridge, MA: MIT Press; 200929. Guston DH. Stabilizing the boundary between US politics and science: The role of the Office of
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33. Jasanoff, S., Technologies of Humility: Citizen Participation in Governing Science. Minerva. 2003; 41(3): 223-244.
Chapter 3
Analyzing the contributions of a government-
commissioned research project: a case study
Published: Health Research Policy and Systems 2014, 12 (1):8
Ingrid Hegger
Susan W.J. Janssen
Jolanda F.M. Keijsers
Albertine J. Schuit
Hans A.M. van Oers
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44 | Chapter 3
Abstract
Background
It often remains unclear to investigators how their research contributes to the work of the
commissioner. We initiated the ‘Risk Model’ case study to gain insight into how a Dutch
National Institute for Public Health and the Environment (RIVM) project and its knowledge
products contribute to the commissioner’s work, the commissioner being the Health Care
Inspectorate. We aimed to identify the alignment efforts that influenced the research project
contributions. Based on the literature, we expected interaction between investigators and
key users to be the most determining factor for the contributions of a research project.
Methods
In this qualitative case study, we analyzed the alignment efforts and contributions in the Risk
Model project by means of document analysis and interviews according to the evaluation
method Contribution Mapping. Furthermore, a map of the research process was drafted and
a feedback session was organized. After the feedback session with stakeholders discussing
the findings, we completed the case study report.
Results
Both organizations had divergent views on the ownership of the research product and the
relationship between RIVM and the Inspectorate, which resulted in different expectations.
The RIVM considered the use of the risk models to be problematic, but the inspectors had
a positive opinion about its contributions. Investigators, inspectors, and managers were
not aware of these remarkably different perceptions. In this research project, we identified
six relevant categories of both horizontal alignment efforts (between investigators and key
users) as well as vertical alignment efforts (within own organization) that influenced the
contributions to the Inspectorate’s work.
Conclusions
Relevant alignment efforts influencing the contributions of the project became manifest at
three levels: the first level directly relates to the project, the second to the organizational
environment, and the third to the formal and historical relationship between the
organizations. Both external and internal alignments influence the contributions of a
research project. Based on the findings, we recommend that research institutes invest
in a reflective attitude towards the social aspects of research projects at all levels of the
organization and develop alignment strategies to enhance the contributions of research.
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Case study Risk Model | 45
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Background
For knowledge institutes such as the Dutch National Institute for Public Health and the
Environment (RIVM), it is important to know what factors influence the impact of their
research. This article aims to give insight into the process of a government-commissioned
RIVM research project and the relevant alignment efforts needed to enhance its contributions
to the commissioner’s work.
The RIVM is an independent knowledge institute with expertise in the fields of public
health, infectious diseases, health care, medicines, lifestyle, nutrition, and environmental
safety. Being a governmental institution, the RIVM conducts research on behalf of other
governmental organizations to support them in their policy-making and supervisory tasks.
One of the RIVM’s principal contracting agencies is the Health Care Inspectorate (hereafter:
Inspectorate), which supervises the quality of health services, prevention measures, and
medical products in the Netherlands. In a yearly program cycle, the Inspectorate submits
knowledge questions to be answered by research conducted by the RIVM (Additional
file 1 Yearly cycle for RIVM research in commission of the Health Care Inspectorate).
For commissions to the RIVM, the Minister of Health puts a dedicated budget at the
Inspectorate’s disposal, which means that the Inspectorate cannot use this budget for
other purposes. Although RIVM investigators and inspectors interact during all phases of
the research project, the Inspectorate, as the commissioning body, does not have authority
over the research methods used, nor the outcome of studies as is laid down in the Act on
the RIVM [1].
These days, the Inspectorate has to account for the effectiveness of its supervisory methods
[2]. In its long-range plans, the Inspectorate expresses its objective to develop and use
scientific knowledge for evidence-based supervision [3, 4]. Consequently, research projects
commissioned to the RIVM are often intended to contribute to the scientific basis of the
Inspectorate’s work.
An evidence-based approach assumes that use of knowledge will lead to better professional
practices resulting in both better and more legitimate outcomes [5, 6]. This assumption
strengthens the investigator’s expectations with regard to how research products will be
used: investigators will produce scientific knowledge for the professionals, who will be
eager to use it to improve their professional practices. However, this expectation often does
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46 | Chapter 3
not come true: utilization of research findings is difficult to achieve in practice. By now,
the widely recognized difficulties in actual contributions of research have led to extensive
research on knowledge utilization in health care and public health. Knowledge institutes
use the insights from this research field in specific strategies to enhance the likelihood that
their research will indeed contribute to improvements in practice; we call these strategies
alignment efforts [7]. The RIVM also recognized the importance of alignment efforts and
established them into procedures and guidelines on an institutional level. Some examples
of such official alignment efforts are periodic meetings between managers of the RIVM and
the commissioning organizations, training of project leaders where they learn to keep in
touch with the commissioner’s contact person, and guidelines for the periodic progress
reports and final RIVM products.
The RIVM’s aim is to support the Inspectorate in its supervisory tasks and tries to enhance
its contribution to the Inspectorate’s work by specific alignment efforts. However, it often
remains unclear for RIVM investigators to what extent their research really contributes and
how its contributions could be improved. As a part of an RIVM strategic research project on
improving knowledge utilization, we initiated a case study to explore how a RIVM project
proceeded [8].
The objective of this study was to gain insight into how an RIVM project, including its
knowledge products, contributed to the Inspectorate’s work and to identify the alignment
efforts in the research project that influenced the research process and its contributions. In
this article, we first present our study framework, the method used, and our findings in a
‘map’ of the RIVM research project. We describe the research project’s contributions and
the alignment efforts that influenced the project. We finally reflect on the method used,
especially on the feedback session with inspectors, investigators, and managers, as well
as on the study limitations. In our conclusions, we provide also suggestions for improving
research projects and its contributions.
Study framework
The starting point for our study was the awareness that interaction between investigators
and the intended users of research is generally considered the decisive factor to enhance
the contribution of research. Based on the Interaction Model for research utilization in
the field of health policy-making, de Goede et al. [9] developed an analytical framework
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Case study Risk Model | 47
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that consists of a distinct policy network and a distinct research network. In the overlap of
these networks, interaction takes place between the policy network and research network
promoting research utilization (Figure 3.1).
In a way, this model also describes the context of RIVM research for the Inspectorate:
both are distinct organizations with their own networks and they overlap at different
levels. The two networks ‘RIVM’ and ‘Inspectorate’ specifically overlap in the research
projects commissioned by the Inspectorate. Both organizations recognize the importance
of interaction during the research project for the contributions of a research project as
reflected in institutionalized alignment efforts.
Barriers:Expectation, Transfer, Acceptance, Interpretation
Policy network Research network
Research Use
Context
Figure 3. 1 The interaction model by de Goede et al. (2010) [9]. De Goede et al. visualized the distinct research and the policy networks as partially overlapping circles. In the Interaction Model, policy-making is an interactive and incremental process and extensive interaction between investigators and policy-makers promotes research utilization. In the overlap of these networks, interaction takes place between the policy network and research network promoting research utilization.
Although the Interaction Model by the Goede et al. [9] is an adequate model to describe
the overall relationship between the RIVM and Inspectorate organizations, this model did
not offer a method to zoom in on the overlap of the two networks to analyze and explain
the course of a research project. We needed a model for the complex research process
with many different actors on different organizational levels evolving in a certain period.
Contribution Mapping (CM), recently formulated by Kok and Schuit [7], offers a useful
framework for our study, taking into account the social context of a research project and
contains a three-phase process model of the research process. CM also includes a practical
method for analysis, which we applied to our case study.
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48 | Chapter 3
During the research process, the research network and policy network form a hybrid world
(Figure 3.2). Research is a process of co-creation where actors are, on the one hand, the
investigators who perform the research and, on the other, the linked actors who in some
way are connected to the project. Investigators and linked actors go through a joint process
of co-creation in a research project. In this process of knowledge production, the three-
phase process model distinguishes three demarcated phases in which typical activities take
place:
1. Formulation phase: activities to initiate the research process, including funding,
prioritization, and commissioning;
2. Production phase: activities to realize the knowledge products;
3. Knowledge extension phase: activities to make the knowledge available to potential
users and to initiate and stimulate utilization.
It is difficult to assess the final impact of research on action for health and to measure the
actual use of research products. A direct link from a research product to improved practices
is often hard to trace. To handle this attribution problem, Kok and Schuit introduced the
concept of contribution to action: “Contribution to refers to the activities which turn novel
combination of knowledge into a ‘going concern’, as part of practices, a component of
successful innovation, as an element in decision making and their implementation” [7]. All
phases of the research process can be relevant for contributions to health practices and Kok
and Schuit distinguished four categories of research-related contributions:
1. Changes in abilities and actions of involved and linked actors due to the research
activities;
2. The contributed knowledge products as such;
3. Contributions through the utilization of the produced knowledge by investigators
and linked actors;
4. Contributions through utilization at distance by non-linked actors.
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Case study Risk Model | 49
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Figure 3.2 Three Phase Model by Kok and Schuit [7]
In research projects, actors are usually aware of problems in research transmission and
utilization. They therefore design alignment efforts; during all phases of the research
process, both investigators and linked actors undertake specific actions to enhance
the desired contributions of the research process and the likelihood that the research
indeed contributes and that the research products are used. Actors have their own actor-
scenario which may have (decisive) influence on the process in all phases and thus on the
contributions of the research process, on the knowledge product and/or utilization of the
knowledge product. In practice, actors are not only involved in one research project, but
are part of their own network and organizational environment and their actor-scenario
continuously evolves. Kok and Schuit describe knowledge utilization as “incorporating
knowledge into an actor-scenario as a means of contributing to its strength and scope” [7].
For incorporation into an actor-scenario, research knowledge has to be translated into a form
and content that fits the actor-scenario. Alignment efforts will be most effective to enhance
contributions of research knowledge when investigators and involved actors recognize and
take account of the different actor-scenarios. Based on the three-phase process model, Kok
and Schuit developed a method to systematically evaluate the complex research process
and the contributions of the research to action. According to this CM evaluation method,
the investigators of a research project and the linked actors, such as potential key-users,
are interviewed after an initial document analysis. Based on the findings, a map of the
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50 | Chapter 3
research process is drafted taking alignment efforts and an estimation of the contributions
into account. In a feedback session, the draft map is presented to relevant stakeholders to
validate the findings and to identify inconsistencies. Next, the contribution map is finalized
and used for learning, improvement, and accountability purposes [7].
In our case study, we used the three-phase process model of CM as a study framework
and we used the CM evaluation method to investigate the RIVM project ‘Risk Model’,
commissioned by the Inspectorate, and its contributions. We specifically focused on the
interaction between actors, especially the investigators and key users, using the theoretical
concept of CM that alignment is the precondition for the contributions of a research project.
Alignment efforts to create alignment are important to enhance its contributions; Kok and
Schuit described various alignment efforts such as “engaging potential users in setting
research priorities, formulating research and interpreting results, employing double-role
actors in research and disseminating research results to potential key-users” [7]. In our case
study, we inductively identified the alignment efforts that appeared to be relevant for the
RIVM-Inspectorate relationship.
Methods
To explore the contributions of a RIVM project to the work of the Inspectorate, we used a
qualitative case study approach, including document analysis and semi-structured interviews
[10]. This case study concerns the Risk Model project, a small project with a limited number
of involved actors commissioned by the Inspectorate during three consecutive years.
Contribution map
For the document analysis, we manually analyzed documents from the project archives
within the RIVM and relevant public documents of the Inspectorate in order to reconstruct
the course of events with respect to the project. We interviewed actors from RIVM and
the Inspectorate involved in theproject (n=10),namely the investigators (RIVMproject
leader and another RIVM investigator), the key users (four inspectors), and two RIVM
managers and two managers from the Inspectorate as relevant informants. We used a topic
list consisting of items regarding the research process, the actors and their organizational
environment, the interaction between actors, and the contributions in the three phases of
knowledge production, all based on the CM evaluation method. An additional file shows
this in more detail (Additional file 2 Topic List interviews actors Case Study Risk Model). The
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Case study Risk Model | 51
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RIVM principal investigator, who was also involved in the Risk Model project, conducted the
semi-structured interviews face to face. Each interview lasted approximately one hour and
was recorded and transcribed verbatim.
After importation of the data into Atlas-ti version 6.2.25, the principal investigator analyzed
the data by coding [11]. We based the code list initially on the conceptual framework and
completed it with inductive codes. The coding of the interviews started while data collection
was ongoing and the topic list for the interviews was iteratively adapted in order to achieve
data saturation. Three other investigators independently coded two interviews and we
validated the coding in an open-coding session (agreement 72%; response 70%).
Based on the documentary analysis and interview data, we constructed a map of the
research project according to the method CM by assessing the course and contributions of
the project [7].
Feedback session
Next, we organized a feedback session with two inspectors, a manager from the Inspectorate,
the RIVM project leader, and a RIVM manager, to present and discuss our findings. All those
present gave their feedback on the draft assessment and discussed actions for improving
contributions and interaction. This discussion was recorded and transcribed verbatim. Based
on the findings and the outcome of the feedback session, we drafted the final version of the
contribution map and we inductively identified six categories of relevant alignment efforts.
Results: the research process and its contributions
In this section, we present the course of the research process based on the data collected
by documentary analysis and the interviews. We identified contributions in three
categories: the utilization of the produced knowledge by inspectors, investigators and their
organizations (contributions through linked utilization), the project’s knowledge products
(contributed knowledge products), and changes in abilities and actions by inspectors,
investigators and their organizations due to the research project (change in involved and
linked actors). Contributions through utilization at-a-distance, the fourth contribution
category distinguished by Kok and Schuit, did not emerge due to the confidential nature
of the knowledge products [7]. In brackets, we name the identified contributions and the
occasions where we observed the presence of alignment efforts.
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Background of the project
The Risk Model project lasted for three consecutive years with an extension in the fourth year
(2007–2010; Figure 3.3). According to the yearly cycle for RIVM research, the Inspectorate
submitted a knowledge question for every project year to which the RIVM made a
corresponding offer. For every project year, we distinguish the three phases according to
CM:
1. The period for submitting the knowledge question and writing the project plan
in an RIVM offer (from July until December; in the preceding year; formulation
phase);
2. The period for performing the planned research activities (from January until the
delivery of all agreed knowledge products; production phase);
3. The period after delivery of agreed knowledge products (extension phase).
The project aimed to develop a risk-based approach for clinical trial inspections in the
Netherlands and had to deliver risk models to enable ranking and stratified selection of
clinical trials for inspection. The research activities included the identification of risk
factors and risk indicators and the development of two risk models: one for clinical trials
on medicinal products (1st year) and a second for clinical trials on food substances (3rd
year). We consider the models contributed knowledge products according to CM. To create
these knowledge products, a synthesis of scientific knowledge on risk-ranking, risk models,
medicinal products, and food substances was made and combined with legal and practical
knowledge on clinical trials and inspections. This resulted into a new risk-based approach to
clinical trials. For this project, the RIVM performed desk research in close collaboration with
inspectors of the Inspectorate, without involvement of other organizations.
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KQ 1 Development model 1
2010200820072006 2009
Delivery risk model 1 Use of risk model 1
Deliveryrisk model 2
(no use)
Implementation risk model 1Development risk model 2
Formulation Phase : formulation of knowledge question (KQ)
Production Phase
Extension Phase
KQ 2 Sleep mode
KQ 3
Project cycle 1
Project cycle 2
Project cycle 3
Figure 3.3 Timeline for the risk model project. Timelines of the Risk Model project visualizing the formulation, production, and extension phase for the three project cycles. In the formulation phases, the knowledge questions (KQ) were: 1) the development of risk model 1 (KQ 1), 2) the implementation of risk model 1 (KQ 2; postponed to project cycle 3), and 3) the implementation of risk model 1 and the development of risk model 2 (KQ 3). In the production phases, the following activities took place: 1) the development of risk model 1 (production phase 1), 2) no activities, project in sleep mode (production phase 2), and 3) the implementation of risk model 1 and the development of risk model 2 (production phase 3). Risk model 1 has been used in extension phase 1, risk model 2 has not been implemented or used.
Development of the first risk model
During the first formulation phase, the RIVM project leader and the contact person of the
Inspectorate agreed to focus on clinical trials on medicinal products (alignment efforts;
Formulation Phase 1).
Although in line with the official policy plan of the Inspectorate, the inspectors emphasized
that it was not the driving force behind their research question; they felt the need for a
tool for risk-based selection of inspection objects because of the overwhelming number of
clinical trials they had to supervise (about 1,800 approved protocols each year). Although the
inspectors were of the opinion that they had the expertise and competencies themselves,
they had no time to develop a method for risk-based selection. They formulated an official
RIVM knowledge question including distinct ideas for the approach of the problem and the
design of a tool.
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Inspectorate Manager 1: “The knowledge question came up because of the enormous
amount of inspection objects and the small number of inspectors involved. They tried
to find a sensible way for risk-based selection.”
At the RIVM, the origin of the research question was less clear. Some RIVM respondents
thought the Inspectorate’s managers ordered the risk-based approach because of the
official policy.
Researcher 1: “I think that the knowledge question came from higher quarters, because
of the general wish to have more risk-based supervision, just because of the general
principle and to have a model for it.”
After the formal start of the first production phase, it took several consultations to refine
the research question and to agree upon the way to go (alignment efforts; Production
Phase 1). This exploring phase in the production phase took longer than foreseen by the
RIVM investigators in the project plan and caused delay. The data accessibility appeared to
be much more problematic than anticipated, because the Inspectorate could not directly
access the clinical trial database that is in control of another governmental organization,
which largely hindered the development of the risk model.
The research team consisted of three RIVM investigators, who cooperated closely with
three inspectors. During meetings, they discussed the scientific approach of risk ranking,
risk factors, indicators, and draft versions of the risk model (alignment efforts). The project
resulted in an electronic risk model and a report on its development (contributed knowledge
product).
The transfer of the knowledge product by mail was without any project-specific dissemination
activities and six months later than originally planned (Extension Phase 1). After transfer, the
inspectors mentioned to the investigators that their management criticized the risk model.
However, the inspectors internally solved the issue and the nature of the criticism never
became clear to the investigators. In the interviews, the Inspectorate’s managers expressed
some critical remarks on the scientific approach of the risk model but also mentioned
that the inspectors involved were contented with the model and that this was decisive for
accepting the knowledge product.
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Researcher 1: “And I became aware that manager 2 at the Inspectorate had a negative
opinion and we asked for more explanation, but we never received it.”
Since the risk model was considered an internal confidential inspection tool, the Inspectorate
requested to keep the model confidential. The RIVM agreed although it meant that they
could not further publish it nor use it in scientific discussions on risk-based supervision
(alignment efforts).
On their side, the inspectors did not disseminate the risk model, neither in their external
network due to its confidential status nor within the Inspectorate, because they were of the
opinion that the risk model was too specific for other disciplines within the Inspectorate.
The only occasion they exchanged the risk model was during the discussion with another
governmental organization to get access to the clinical trial database (contributions
through linked utilization). Nevertheless, they shared their experiences with the model in
international discussions on risk-based inspections (contributions through linked utilization).
The Inspectorate also mentioned the existence of the risk models in public presentations, in
publications, such as annual reports, and in a formal answer to questions of the Parliament
(contributions through linked utilization).
Project in ‘sleep mode’
During the second formulation phase (that coincided with the first production phase), the
Inspectorate formulated a new knowledge question: their intention was to incorporate
the risk model in their operating procedures and they asked for RIVM assistance in the
implementation (Formulation Phase 2).
After the official start of the second production phase, it eventually became clear that the
inspectors could not realize the implementation of the risk model due to shortage of staff at
the Inspectorate. Consequently, they did not need RIVM-assistance and the project went into
‘sleep mode’ (Production Phase 2). In fact, the yearly cycle was broken due to unforeseen
circumstances and the Inspectorate officially postponed this knowledge question to the
next (third) year.
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Implementation and a second risk model
For the third year, the knowledge question included both assistance at the implementation
of the risk model and the development of a second risk model for another category of clinical
trials (Formulation Phase 3). In their offer, the RIVM investigators did not yet define the
category of clinical trials for this second model, but mentioned two options as an example.
They stipulated that the choice for the new category should depend on the availability of
appropriate data after an inventory of available data.
An RIVM investigator assisted at the implementation of the risk model for clinical trials on
medicinal products and adapted the original model in order to facilitate data import into the
model (alignment efforts; Production Phase 3). In June, a short report was presented to the
Inspectorate on the progress, including the adapted electronic risk-ranking tool for clinical
trials on medicinal products (contributed knowledge product).
For the second risk model, the investigators and inspectors initially disagreed on the
category of clinical trials. Due to a serious incident in a Dutch hospital in the previous
year, the inspectors wanted clinical trials on food substances to be the focus of the second
model. The investigators preferred clinical trials on medical devices based on the analogy to
medicinal products, more available data and the match with their own expertise. However,
the Inspectorate’s reality is that they also have to take into account the public and political
circumstances when setting priorities in supervision and they felt the need to develop a risk
model for a category that was less obvious for the researchers. This caused some tension
in the project between investigators and inspectors, which was eventually resolved by
discussion (alignment efforts).
The development of the new risk model for clinical trials on food substances needed extra
unforeseen time and was not delivered according to the project plan but in the following
(fourth) year (contributed knowledge product). During the finalization phase, only the RIVM
project leader was involved and occasionally consulting other investigators. The model was
again confidential and not published on the RIVM website. The second risk-model on clinical
trials with food substances was never used (Extension Phase 3).
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Interviewer: “What is your opinion about the second model, did you use it?”
Inspector 3: “No, I cannot say anything about that because we did not use it until now.”
Interviewer: “Could you indicate what the reason is?” Inspector 3: “Mainly because of
competition with other tasks or other inspections. There were other issues with priority:
international inspections and the thematic inspection project. And because the priority
of the second category inspection objects decreased, the incident was dealt with and
the interest in these inspection objects diminished.”
Sequel to the project
The investigators and inspectors had differing views on the desired sequel to the project
which uncovered differing views on the ownership of the knowledge products. On one hand,
the investigators regarded the risk models as their own knowledge products or at least co-
creations with co-ownership of both parties. They expected that further development of the
risk models would also evolve in co-creation by RIVM and Inspectorate and that they would
spontaneously receive feedback on user experiences with the model.
Researcher 1: “…I have the opinion that they should exchange this kind of information
spontaneously.”
The inspectors presented their risk ranking experiences in EU expert meetings, but did not
provide feedback to the investigators; they were not aware that international discussions
on a risk-based approach were of high interest to the investigators. They regarded the
risk models as their own products and they choose not to involve the investigators in
the evaluation and further validation of the models. The confidentiality of the products
conflicted with the investigators’ interest to publish the reports and to use the findings in
international discussions. Although both RIVM management and the investigators agreed
with the required confidentiality, these differing expectations were discussed neither at the
start nor at the end of the project causing unarticulated tension.
Appraisal of contributions
All inspectors were rather satisfied with the contributions of the project to their work. In
their opinion, they had used the risk models as much as possible and they expected further
use, validation, and development of the models in the future (alignment efforts). However,
the need for linking the risk models directly to the clinical trial database became gradually
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evident after transfer, but access to the database remained problematic. Without linkage to
the database, the risk models turned out to be too laborious. Nevertheless, the inspectors
were determined to move on with the models in coming years.
Inspector 2: “Yes, I feel positive about it. Especially inspector 3 used it and in that sense
I have the impression that the worksheets, the Excel sheets, function properly.”
The Inspectorate’s managers were positive about the project afterwards, merely because
the inspectors as users of the models were positive (alignment efforts). However, they
showed some reserve since the risk models could only be in full use if connected to the
clinical trial database. Given that this feature was not yet realized, the risk models had not
taken away the managers’ concerns about the supervision of clinical trials. They still felt
the need to have ways to predict specific, yet unknown risks in order to be able to prevent
incidents and they doubted whether the current feature of the risk models was suitable for
this purpose.
Inspectorate manager 2: “We should think more about what we want to know and
what we want to do with it at the start. We consequently do nothing with the report.
Although this was not a bad example after all, since the inspectors felt contented about
it. But it can be improved.”
On the other hand, the RIVM investigators assessed the contributions of the project to
the Inspectorate’s work as minor. After transfer, they were insufficiently acquainted with
the implementation problems at the Inspectorate. They had expected that the risk models
would be used on a daily basis within two or three years.
Researcher 1: “I expected that we would establish a model able to scan all clinical trials
within a maximum period of two, three years.”
Interviewer: “For all trials?”
Researcher 1: “For all trials, yes, but to achieve that more thinking, more communication
was needed and it had to be done faster. But it did not work out that way…”
At the site of the RIVM, the project contributed to the implementation of their strategy
to extend the research area of the centers specialized in the quality control of medicinal
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products. The required expertise on risk ranking was on the fringe of the traditional expertise
of the RIVM centers involved and the project offered the opportunity for developing new
expertise (contribution ‘change in involved and linked actors’). However, this contribution
was hindered by the confidentiality of the risk models.
Consultative structure
In this study, we paid special attention to the interaction in all phases of the research project
and we also found that all interviewed persons in this case study recognized the importance
of their interaction to enhance the contributions of the research project. We asked them
to indicate which factors could improve the process and contributions, and they all
spontaneously indicated that the relationship and interaction like meetings and continuous
consultations are crucial for success in a research project.
During the phase of formulation, the investigators and inspectors had only limited
interaction. The formal procedure agreed between the Inspectorate and RIVM does not
facilitate in-depth discussion on the knowledge question and the project plan due to the
very formal deliberations at management level, short time periods, and strict deadlines
within the procedure.
Inspectorate Manager 2: “The more the question is vague, the more RIVM is not able to
make a proper offer. If it is too unarticulated, the RIVM should not accept the question.
What would the offer be based upon, which expertise and how many research hours?
We should have more interaction.”
During the production phases, the consultations went on in a good atmosphere according to
both parties. In meetings, the inspectors and investigators openly discussed the risk factors
and drafts of the risk model (alignment efforts).
Inspector 4: “It was according to an established pattern. We discussed what we as
inspectors thought about the results so far and then the RIVM got the work again to
improve (the drafts).”
The frequency of the consultations between RIVM and the Inspectorate depended much on
proactive organization, availability of persons, and priorities at the Inspectorate (alignment
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efforts). The interaction between investigators and inspectors often suffered from time
constraints and the inspectors and investigators experienced this in a different way.
The inspectors considered the frequency of interaction overall rather high and satisfactory,
especially in the first year. The investigators emphasized that the lack of time of the
inspectors to give feedback on drafts of the risk model resulted in delay. Although the
inspectors regretted that their own time constraints delayed the evaluation and further
development of the model, they accepted this fact of life.
Inspector 2: “At the start, I think the intensity was very adequate, meetings on fixed
time points. It is my feeling that there was need for it. The meeting dates were planned,
but only used if needed. At a certain point in time, my role changed and I did not
take part in everything anymore and therefore it is difficult for me to assess. It is my
impression that it was less frequent for the extra model; however, this was the second
project and things were clear already. So, although less frequent, it was sufficient in
relation to the need.”
Interviewer: “What is your view on the interaction with the inspectors?”
RIVM Manager 2: “With great difficulty, at least between RIVM and Inspectorate and
I have the impression that the inspectors get so many stuff and small issues on their
desks that they have difficulty to pay attention to structured campaigns and they spent
a lot of time in acting in a reactive way. I suppose…, this is my impression.”
Organizational environment
At the RIVM, the Risk Model project was a rather isolated project that lacked solid
embedding in the research organization because the project was unusual and small in terms
of people involved and research hours available. Colleague investigators were busy with the
regular, large projects and not very interested because of the limited link with their research
activities. The investigators had a few deliberations with their management to monitor
the progress of the project at formalized moments (alignment efforts). The managers
controlled the finances and timely output, but maintained their distance to the project and
only commented on drafts of the final report (alignment efforts). At management level,
meetings between the Inspectorate and the RIVM only focused on general issues and the
Risk Model project was never discussed. The managers discussed neither the contributions
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of the project nor a way out for the confidential status of the knowledge products in order
to facilitate publication of findings.
Investigator 2: “We worked rather solitary. I experienced it as an isolated project,
detached, isolated. It was not attached to other projects at all. It was not interwoven
with the RIVM network.”
An important finding was the major influence on the project of the established relationship
between both RIVM and the Inspectorate. In the interviews, the inspectors, investigators,
and managers expressed strong ideas of the other organization and we observed divergent
views on the mutual relationship. At management level, the budget system was always an
important issue since the Minister of Health does not allow the Inspectorate to use their
dedicated RIVM-budget for commissioning research to other organizations. The Inspectorate
considered the system therefore as a forced sourcing system without competitors for the
RIVM and without sufficient possibilities to influence the RIVM research proposals. This
view is in contrast with the perception of the RIVM managers and investigators, who
considered their research for the Inspectorate as working on a mutual governmental task
and experienced the Inspectorate’s view as unjustified distrust of their organization.
Inspectorate Manager 1: “There exists a very negative view on the RIVM. Not with
respect to their quality, but because we have this forced sourcing at the RIVM.”
RIVM manager 1: “The Inspectorate relies on RIVM results, but the forced sourcing
reflects the relationship and this causes lack of trust.”
On their side, the RIVM managers experienced that lack of time largely determined the
quality of the Inspectorate’s commissioning role often resulting in unarticulated research
questions. Because the RIVM accepted all research questions, this often led to unsatisfactory
contributions of research projects.
RIVM Manager 1: “So it was a knowledge question and actually, you were told to
elaborate it per definition. So the only choice we had, was to choose the way to deal
with the knowledge question, but not whether you should deal with it at all, that was
no consideration at that time.”
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Discussion
Relevant alignment efforts
Analyzing the course of the Risk Model project and as indicated in the findings, we observed
alignment efforts made by both RIVM and the Inspectorate; investigators, inspectors, and
managers tried to create alignment within the bounds of their reach, both according to
the institutional procedures at stated moments and according to the circumstances in the
project. The importance of well-organized interaction between the networks RIVM and the
Inspectorate is recognized on an institutional level; the RIVM and the Inspectorate have
agreed upon transparent formal procedures to streamline the yearly commissioning process
and to monitor the course of the agreed research projects. The Risk Model project was
managed according to these formal rules and procedures. De Leeuw et al. [12] described a
classification of 30 different theoretical frameworks for dealing with action on the nexus of
research, policy, and practice. They established three groups of seven categories of theories,
one of them the category Institutional Re-design. This category comprises theories that
acknowledge the importance of interactions between actors from different institutions,
which results in the explicit management of these interactions by maintaining institutional
arrangements and establishing institutional rules. In our view, alignment efforts by the
formal procedures match with strategies in the category Institutional Re-design. For both
RIVM and the Inspectorate, alignment rules and guidelines were top-down established and
explicitly encouraged project leaders and contact persons to interact with their counterpart
at the other organization during formulation and production phase of a research project.
Their management boards jointly discuss and revise regularly the agreed procedures to
improve commissioning process. For the extension phase, the RIVM procedures provided
guidance and rules for the presentation and layout, formal approval by the management
and the transfer of contributed knowledge products.
Despite these institutionalized alignment efforts, we observed difficulties that could be
attributed to lack of alignment at the level of the research project. Based on the course
of the project and the contributions as described in the results section, we inductively
identified six categories of alignment efforts that were relevant for the project.
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Relevance: discussing the research results and their relevance for the commissioner and
attuning the presentation of the knowledge products to the needs of the commissioner
Our findings show that the investigators and inspectors translated the need for alignment
mainly in alignment efforts on ‘relevance’. The importance of alignment was in fact well
recognized by the investigators and inspectors in the Risk Model project; they developed
the two risk models as much as possible in close collaboration. During the production phase,
alignment efforts primarily focused on discussing the concepts and drafts for the risk models
and on the design of the electronic tool. From the perspective of both investigators and
inspectors, alignment efforts on relevance were crucial for successfully accomplishing the
research project. The investigators had to account for both scientific quality and customer
satisfaction and the inspector’s interest was to get timely knowledge products that fitted
to their needs, which required alignment on the level of the scientific aspects and the
presentation of the results.
Together, they also had to deal with the tension that exists in commissioned RIVM research
projects; the RIVM has an independent status established by law and in principle, the
commissioner cannot determine research methods, influence the outcome of studies or
prevent publication of results [1]. At first sight, the formal independent RIVM position
conflicts with the need to align on ‘relevance’ issues. Here, the concept of backstage and
frontstage work formulated by Goffman is helpful to overcome this contradiction [13].
Bekker et al. [14] described the RIVM as a boundary organization in the context of the Public
Health Status and Forecasts (PHSF) reports and the biannual Dutch Health Care Performance
reports. As a boundary organization, RIVM projects act as intermediary entities into which
organizations delegate actors to contribute to the research and where frontstage and
backstage work are combined in order to enhance the influence of the reports in informing
public health policy. At the frontstage, organizations present themselves in their formal
positions, whereas at the backstage, informal alignment paves the way for the organizations’
accountability at the frontstage. By analogy with the PHSF, the RIVM research projects for
the Inspectorate could also be considered boundary areas where research for the benefit of
the Inspectorate is performed and investigators, inspectors, and their managers collaborate.
From this perspective, the formal agreed procedures represented the frontstage work to
account for the organizations’ roles in the commissioning process. The meetings between
the investigators and inspectors and their informal interaction at a personal level can be
considered the backstage.
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Consultative structure: agreeing on and acting on the consultative structure
For the Risk Model project, a limited consultative structure existed that mainly focused
on the production phase. Van Egmond et al. [15] described the infrastructure developed
by the RIVM for the above mentioned PHSF report, indicating that the backstage was
well-organized, and presented it as an example for successful boundary work. However,
in the Risk Model project, a backstage area at the start of the new project hardly existed
and backstage work was limited to a few phone calls. Ample opportunity for backstage
interaction, already in an early phase of the research project, will enhance the identification
of possibly influencing factors and trust between actors and thus improve the process and
its contributions. For the third project year, the opportunity existed to discuss the next year’s
project plan during the regular meetings, but this opportunity was not intensively used. This
shows that backstage work is not only a matter of available time, but also of culture and
relationship between organizations. As argued by Wehrens et al. [16], a well-functioning
boundary organization needs “internal room to discuss different perspectives, goals and
expectations (and to find a balance that satisfies everyone involved) while the legitimacy of
the activities, products and projects is not questioned in the broader organizations of the
participants.” For the case of the Risk Model project, the internal room for backstage work
was limited due to priority setting in both organizations and the relationship between RIVM
and the Inspectorate that interfered with open discussion. The transition from the informal
backstage to the formal frontstage was not clearly marked since the project continued for
several years and, each year, new backstage work had to be done. Inspectors had to take
both frontstage and backstage positions at the same time, causing confusion at the side of
the investigators. In fact, the backstage was not very well developed and the organizations
did not sufficiently recognize its importance in relation to the frontstage.
According to Wehrens et al. [16], the backstage and frontstage of organizations have different
functions but are interrelated and cannot exist independently of one another. In most cases,
the frontstage is predetermined by official arrangements that can even be emphasized by
a ceremonial public presentation of the knowledge product to the commissioner. However,
in the Risk Model project, the frontstage was marginalized because of the requested
confidentiality of the risk models. Because of this, the Inspectorate did not have to account
for using the risk models, which distorted the backstage space and made the investigators
confused about the demarcation of backstage and frontstage.
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Goal and timing: discussing and agreeing on the formulation of the knowledge question,
its origin, the question behind the knowledge question, and the underlying need for the
knowledge products
For three consecutive years, the Inspectorate formulated knowledge questions for the
Risk Model project. The procedure for commissioning research to the RIVM was rather
formal, with strict deadlines, and included several management levels for approval. The
management regularly updated the rules with the intention to improve the research projects
and their contributions. These formal procedures are important for legitimization of the
research projects, but offered limited opportunity for alignment efforts at the investigator
and key user level in the formulation phases. Although the formal alignment efforts with
respect to the goal and timing of the project were in line with the established procedures,
several interviewees mentioned that more informal interaction during this phase of a
research process could improve its contributions. These findings are in line with the critical
key factors identified by De Goede et al. [9] to influence the expectations of research users.
Early extensive alignment efforts between investigators and key users on the formulation of
the research question using previous experience and researchers’ knowledge, exploring the
actual needs behind the question, and taking into account study limitations is important to
manage the expectations on the contributions and achievable timelines at both sides.
Tasks and authority: explicit discussing of the relationship between actors and agreeing upon
input and role of actors, responsibilities, sharing of information and knowledge, authority
over the contributed knowledge products, and the follow-up of the research project
In the Risk Model project, the RIVM project proposals, as presented in the formal offers, were
designed according to the formal guidelines and approved by both the RIVM management
and the Inspectorate. However, the guidelines did not explicitly require consideration of
time investment by the inspectors, the ownership of the knowledge products, the exchange
of confidential information, and the follow-up of the project, whereas these issues caused
friction later in the project. The alignment strategies based on the Institutional Re-design
approach were not able to meet the need for mutual understanding between organizations
at project level. Another category of theoretical frameworks described by De Leeuw et al.
[12] is the Blurring the Boundaries model. In this model, the actors of organizations involved
learn about each other’s world by obtaining access to it. In our study, a notable finding was
that the RIVM and the Inspectorate afterwards differently assessed the contributions of the
project, the interaction during the research process, and the ownership of the knowledge
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products. Investigators and inspectors had different actor scenarios, but were not aware
of this. This illustrates the need for more alignment strategies based on the Blurring the
Boundaries model. Understanding each other will generate more trust and confidence,
better recognition of perceptions and more open discussions on sensitive issues. Every
actor in a research process has his/her own scenario and perspectives for the future of the
research project contributions. If investigators are aware of the changing circumstances in
the commissioner’s organization and understand the role knowledge and research projects
have in the commissioner’s scenario, they will be better able to promote the research
contributions.
Vertical alignment: sharing information within the own organization and embedding of the
research project within the own organization
In the literature, the importance of horizontal alignment between research and key
users is exhaustively described; horizontal alignment efforts are considered the key for
enhancing research contributions. We observed that also the vertical alignment within the
own organizations of both investigators and inspectors was a very relevant factor for the
research process and its contributions. Some difficulties in a project with respect to tasks
and authority, relevance, and organizational environment cannot be tackled by investigators
and linked actors at a project level and will often ask for a combination of horizontal as
well as vertical alignment efforts at different levels in the organizations. The embedding
of Risk Model in both RIVM and the Inspectorate was limited and the management was
hardly involved during the production process, while their alignment efforts focused on
general issues and not on project-specific issues. We argue that explicit vertical alignment
efforts could bring project-specific issues to the attention of the management level at which
horizontal alignment efforts could really enhance the solutions. The required confidentiality
of the risk models serves as an example of a fundamental issue where vertical alignment
efforts were lacking. The Inspectorate desired confidentiality because publication would also
mean that they had to justify the selection criteria in the risk models to outside stakeholders
and that they could no longer diverge from the selection method. On the other hand, the
RIVM’s task and interest was to deliver scientifically legitimate knowledge products and,
to achieve this, both the necessity of stakeholders’ involvement and publication of the risk
models should have been considered. The inspectors were bound to their own organizations’
policy and the investigators met the requirements of the commissioner. Vertical alignment
efforts on project-specific issues would have identified the different views of RIVM and
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the Inspectorate at the appropriate organizational level at an early stage and could have
resulted in a more grounded RIVM position on the ownership issue and scientific approach.
Organizational environment: aligning with respect to relevant conditions outside the
research project influencing the relationship between investigators and linked actors and/or
the research project, such as changing priorities, incidents, media-events, and relationship
with other organizations
In the formulation phase, a new research project is dealt with as a well-defined assignment
that can be planned and controlled by the project manager. In reality, the research project
and its actors are part of a complex organizational environment that continuously changes
and influences the course and contributions of the project. In the Risk Model project, we
identified several unexpected influencing factors from the Inspectorate’s organizational
environment, such as data accessibility, time investment by the inspectors, and a serious
incident that influenced the second risk model. At the RIVM site, implicit, not openly discussed
organizational circumstances, such as the project’s embedding in the organization and the
historical relationship between RIVM and the Inspectorate, appeared to be influencing. On
the one hand, both investigators and inspectors did not exactly know and understand the
underlying feelings and motives of the other organization and their alignment efforts focused
mainly on the scientific issues. On the other, the project’s backstage did not sufficiently
facilitate reflection on the project to develop feelers for influencing factors from the project’s
organizational environment. Conscious alignment efforts on the organizational environment
would require more trust and understanding as argued in Blurring the Boundaries models
combined with a well-developed backstage to accommodate discussions.
Reflection on contribution mapping (CM)
The evaluation method of CM aims to offer a practical and realistic approach to evaluate the
contributions of a research project and to analyze the alignment efforts. In CM, both key users
and investigators have an active role by being interviewed and participating in the feedback
session. Due to these characteristics, this method can be considered a fourth generation
evaluation method [17]. The criteria for assessment of contributions and alignment efforts
are not fixed beforehand, but are based on issues that emerge from the interviews. In our
view, this responsive evaluation was useful to unravel a research project such as Risk Model,
the contributions of which remained, on the face of it, unclear. To elucidate our questions
on research contributions, a qualitative approach taking into account the actors’ own issues
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and their social process was needed to find clues for improvement on both organizational
and project level. By using CM, we indeed gained an illuminating insight in the course of the
Risk Model project. The interviews delivered a rich data set that disclosed the contributions
and alignment efforts. When presenting these findings to inspectors during the feedback
meeting, investigators and managers recognized the analysis and findings, which adds to
the validity of the analysis. The feedback meeting gave opportunity to discuss the differing
views, to exchange experiences, and to formulate concerted actions to solve identified
issues.
We would like to comment that for a small project such as Risk Model, the number of
interviewees can remain limited to get a complete overview. For a major project, we expect
that this would require a proportional number of interviews with a corresponding workload.
Depending on the aim, CM users could consider focusing only on specific key users in order
to conduct the CM with achievable effort. Another possibility for selective application of
CM is to choose a project as a typical example in a specific context. In this case study, we
recognized patterns and issues that are directly applicable to other RIVM research projects
as well.
The concept of contributions was very helpful to identify the (added) value of the project
for the Inspectorate’s work. The project’s attributed value manifested itself not as expected,
but could be demonstrated by the concept of ‘contribution’. The CM method does not focus
on assessment of the contribution category ‘utilization on distance’. In our case, this was not
a drawback because of our focus on contributions to the commissioner’s work to improve
RIVM projects.
Although the first aim of the feedback session was to add information to the collected data
from interviews and document analysis, we experienced that such a feedback session is
an alignment strategy in itself. We drafted an abridged report of the discussion on which
the participants commented. The consensus report included several recommendations for
improvement of the knowledge production process to be taken aboard for future projects
and a proposal for a pilot to test the recommendations in a number of new projects. We sent
the report to managers within both organizations, and we therefore consider the feedback
session as a very useful three-layer part of the case study; the scientific data collection layer
where participants were able to add information or to comment on findings; an alignment
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strategy in itself since the participants solved issues during the discussion; and a method to
improve the research process.
By joining a systematic evaluation session, participants can learn how to improve the
research process [18]. Although in our case all participants valued the feedback session in this
respect, we experienced that the formulated actions for improvement did not automatically
result in better research processes in actual RIVM projects since the agreed actions were
subject to the same alignment problems as the project and turned out to be more complex
than expected during the feedback session. We argue that a carefully planned and managed
follow-up would be the fourth prerequisite of a successful feedback session.
Study limitations
We have to mention some limitations of this study. The principal researcher of this study
was also involved as an investigator in the Risk Model project. As an RIVM investigator, she
is also involved in other projects for the Inspectorate at present. On one hand, she had the
advantage of having inside knowledge about the research process and the context of the
case. To overcome the disadvantage of being biased by own experiences, the coding of the
interviews was validated by three other researchers not involved in the Risk Model project.
The research team intensively discussed the analysis of the findings. Moreover, the findings
were also discussed with the participants of the feedback session. Combining all feedback,
we conclude that consensus on the analysis exists within the research team.
In this article, we describe the first case in a multiple case study on the contributions of
government-commissioned research projects. For this multiple case study, the different cases
are selected to cover a variety of characteristics that may influence the research process and
its contributions. This first case was a relatively small research project within the specific
context RIVM-Inspectorate. This questions to what extend the findings can be generalized
to other research projects. Our findings were largely in line with our expectations based on
the study framework. According to CM, inspectors, the RIVM project leader and managers,
and the Inspectorate discussed the contribution map in a feedback session. They agreed on
the findings and identified general issues that also emerge from other research projects.
Moreover, we presented the final contribution map in several scientific meetings in the
RIVM. The influence of limited interaction, organizational environment, and relationship
with other organizations is widely recognized, also by investigators operating in other
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expertise fields and working with other commissioners. Although this case study describes a
specific and small project, we consider the findings relevant for government-commissioned
research projects. However, we will have more insight in the generalizability of this case
after completion of all cases in our multiple case study.
Conclusions and recommendations
By analyzing the course of the Risk Model project and its contributions, we wanted to
establish which alignment efforts are important for the RIVM-Inspectorate context in
order to find clues for improving the contributions of RIVM projects. We identified six
categories of relevant alignment efforts that can be undertaken at three different levels:
at the first level, alignment efforts between investigators and linked actors; at the second
level, alignment efforts related to the organizational environment of the project appeared
also to be important; at the third level, alignment efforts between organizations as part
of their formal and historical relationship. At the first level, investigators and linked actors
can improve alignment by continuous reflection on actor scenarios, awareness of mutual
expectations, and open discussions with commissioners at all levels in the organization. This
will ask for substantial efforts from all actors involved and will take precious (research) time
for interaction on an ongoing basis.
At the second level, more awareness of the importance of the organizational environment
could help to formulate an adequate response to challenges for the research project for
which vertical alignment efforts can be essential. Since the vertical alignment efforts turned
out to be of influence, the focus in a research project should not only be on the external
alignment efforts. Attention for the role of internal interaction, both at the level of the
project as well as management level, and a good institutional embedding could improve the
research process and thus its contributions.
At the third level, alignment efforts are more difficult to deal with; the historical relationship
of the institutes determines their views on each other at all organizational levels and thus
influences the interaction during the research process. This ‘soft side’ of the project can be
hard to manage and therefore a collective approach at all organizational levels should be
developed. It could be useful to openly discuss the historical relationship and its influences
on the interaction within, and even between, organizations. We suggest that both research
organizations and commissioning bodies should invest time and energy in regularly
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organized reflection sessions where both researchers and managers openly analyze and
discuss the relationship with other organizations. This also implies that maintenance of this
awareness will be important since collective views and memory also influence new actors.
If all actors are continuously aware of the historical context and relational aspects of their
research projects, they could anticipate on the implicit consequences and improve their
alignment efforts. At the strategic organizational level, alignment efforts should focus on
the organizational image to increase trust and legitimacy in order to overcome historically
determined, yet invalid frames.
Based on the findings, we recommend that a research institute should encourage a reflective
attitude towards the social aspects of research projects at all levels in the organization. The
first step for improvement is to validate the importance of the process factors for a new
project; the second step would be to calculate in the need for time for these aspects of the
research process at the start of the project. This will facilitate the third step to anticipate
explicitly on alignment efforts during the research process. With respect to the evaluation
of a research project, we experienced that CM offers an alignment effort in itself, apart
from being a useful instrument to evaluate a research project. The feedback session as part
of CM yielded not only information about the research process and its contributions but
also elicited awareness and preparedness for improving research processes at the side of
the participants. CM can therefore be a useful instrument in reflections on contributions
and research processes. Nevertheless, one should be aware that a feedback session needs
carefully planned follow-up in order to improve the research process; the jointly formulated
actions are in fact new projects themselves and need no less alignment efforts than other
projects.
Organizations, investigators, and all other linked actors should be encouraged to experience
the profits of social investments in research projects and should be rewarded for doing
so. To achieve this, different strategies based on different models should be considered.
Institutional rules incorporated in the organizations ‘quality system’, can facilitate project
teams, but should be coupled with sufficient room for well-organized backstage work
with involvement of actors familiar in both organizations. The challenge is to convince
organizations and their staff to consider alignment efforts as a valuable dimension of
research projects, instead of extra burden, because of its influence on project contributions
and on trust in and legitimacy of the organization in a broader sense.
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References1. RIVM. Wet op het RIVM (In English: Act on RIVM). Available from: http://wetten.overheid.nl/
BWBR0008289/. Accessed on 16 May 2014.2. Gezondheidsraad. Op weg naar evidence based toezicht. Het onderzoek naar effecten van
toezicht door de Inspectie voor de Gezondheidszorg. The Hague: Health Council of the Netherlands; 2011.
3. Inspectie voor de Gezondheidszorg. Meerjarenbeleidsplan 2008–2011 Voor gerechtvaardigd vertrouwen in verantwoorde zorg. The Hague: Health Care Inspectorate; 2007.
4. Inspectie voor de Gezondheidszorg. Meerjarenbeleidsplan 2012–2015 Voor gerechtvaardigd vertrouwen in verantwoorde zorg (II). The Hague: Health Care Inspectorate; 2011.
5. Lavis JN, Oxman AD, Lewin S, Fretheim A. SUPPORT Tools for evidence-informed health Policymaking (STP). Health Res Policy Syst. 2009; 7(Suppl 1):I1.
6. Oxman AD, Lavis JN, Lewin S, Fretheim A. SUPPORT tools for evidence-informed health policymaking(STP)1:what isevidence-informedpolicymaking?HealthResPolicySyst.2009;7(Suppl 1):S1.
7. Kok MO, Schuit AJ. Contribution mapping: a method for mapping the contribution of research to enhance its impact. Health Res Policy Syst. 2012;10:21.
8. Demon JMH. Strategic Research RIVM 2011–2014. Project summaries. Bilthoven, Nederland: RIVM; 2011.
9. DeGoedeJ,PuttersK,vanderGrintenT,vanOersHA.Knowledgeinprocess?Exploringbarriersbetween epidemiological research and local health policy development. Health Res Policy Syst. 2010, 8:26.
10. Yin RK. Case Study Research Design and Methods. 4th rev ed. Thousand Oaks: Sage Publications; 2008.
11. Friese S. Qualitative Data Analysis with ATLAS. Ti. Thousand Oaks: Sage Publications; 2011.12. De Leeuw E, McNess A, Crisp B, Stagnitti K. Theoretical reflections on the nexus between
research, policy and practice. Critical Public Health 2008, 18 (1): 5–20.13. Goffman E. The Presentation of Self in Everyday Life. London: Penguin; 1990.14. Bekker M, van Egmond S, Wehrens R, Putters K, Bal R. Linking research and policy in Dutch
healthcare: infrastructure, innovations and impacts. Evid Policy. 2010; 6 (2):237–253.15. Van Egmond S, Bekker M, Bal R, van der Grinten T. Connecting evidence and policy: bringing
researchers and policy makers together for effective evidence-based health policy in the Netherlands: a case study. Evid Policy 2011; 7 (1):25–39.
16. Wehrens R, Bekker M, Bal R. Coordination of research, policy and practice: a case study of collaboration in the field of public health. Sci Public Policy 2011, 38:755–766.
17. Abma TA. Responsive evaluation: its meaning and special contribution to health promotion. Eval Program Plann. 2005; 28 (3):279–289.
18. Carden F. Issues in assessing the policy influence of research. Int Soc Sci J. 2004; 56:135-151
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Additional files
Additional file 3.1: Yearly cycle for RIVM research in commission of the Health Care
Inspectorate. Textbox describing the yearly research cycle of the RIVM: the formulation of
the knowledge question by the commissioner, the corresponding RIVM offer, the research
phase, and finally, the delivery of the agreed knowledge product.
Additional file 3.2: Topic list interviews actors Case Study Risk Model. The topic list for
the interviews consists of items regarding the research process, the actors and their
organizational environment, the interaction between actors and the contributions in the
three phases of knowledge production. Electronic supplementary material available at
https://health-policy-systems.biomedcentral.com/articles/10.1186/1478-4505-12-8
Chapter 4
Enhancing the contribution of research to health care
policy-making: a case study of the Dutch Health Care
Performance Report
Published: Journal of Health Services Research & Policy 2016;21(1):29–35
Ingrid Hegger
Lisanne K. Marks
Susan W.J. Janssen
Albertine J. Schuit
Hans A.M. van Oers
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76 | Chapter 4
Abstract
Objectives
The Dutch Health Care Performance Report (DHCPR), issued by the National Institute of
Public Health and the Environment (RIVM), aims to monitor health care performance in The
Netherlands. Both the RIVM and the Ministry of Health wish to increase the contribution
of the DHCPR to health care policy-making. Our aim was to identify ways to achieve that.
Method
We used Contribution Mapping as theoretical framework that recognizes alignment
of research to policy-making as crucial to managing contributions to policy-making. To
investigate which areas need specific Alignment Efforts by researchers and/or policy-makers
to enhance the contributions of the DHCPR, we interviewed RIVM researchers and policy-
makers from the Ministry of Health and assessed the process for developing the 2010
version of DHCPR.
Results
We identified six areas where alignment is specifically relevant for enhancing the
contributions of future versions of the DHCPR: well-balanced information for different
ministerial directorates; backstage work; double role actors; reports of other knowledge
institutes; data collection/generation; and presentation forms.
Conclusion
The contribution of health care performance reporting to policy-making is complex and
requires continuous alignment efforts between researchers and policy-makers. These
efforts should form an inseparable part of health care performance reporting and although
this demands considerable resources, it is worth considering since it may pay back in better
contributions to policy-making.
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Introduction
The Dutch Health Care Performance Report (DHCPR) is developed by the National Institute
of Public Health and the Environment (RIVM) to monitor the performance of the health care
system for the Ministry of Health (MoH) in The Netherlands. Based on a scientific framework,
the DHCPR includes indicators for three important public goals: quality, accessibility and
affordability [1,2]. So far, RIVM has published four editions (2006, 2008, 2010 and 2014).
Their primary function is to contribute to ‘strategic policy-making’ and both RIVM and MoH
wish to strengthen this function [3,4].
Knowledge use in policy-making is a complex matter and no simple way exists to improve it.
Weiss characterized three types of knowledge use in policy, often described as instrumental
(data supply), conceptual (formation of an idea) or symbolic (arguments for a certain
position) [5-8].Sometimes, agenda-setting is mentioned as a fourth way [9].For researchers,
instrumental use of knowledge fits into their logic, yet the principal use for policy-making
is conceptual or symbolic [10,11]. Furthermore, socio-organizational contexts influence
knowledge use; knowledge has to coincide with the users’ needs, to be credible to the user
and to reach the user at the right time [12]. To anticipate users’ needs, Lomas pointed out
that linkage and understanding between the policy and research world is important for
enhancing knowledge utilization [13].
A study on how MoH officials used the 2008 version of the DHCPR focused on its utilization
as a ‘desk book’ (instrumental use) but did not take the developmental process of the
report into account [14]. The study concluded that RIVM’s aim to achieve a clear position
for DHCPR in the policy process had not yet been reached. Interaction of researchers and
policy-makers during the developmental process influences utilization of research products
in policy-making [15]. Four clusters of barriers between research and policy have been
suggested which are promoted or obstructed by interaction: expectations, transfer issues,
acceptance and interpretation. In line with this interaction model, Van Bon-Martens et al
demonstrated that next to content and presentational form, the developmental process is a
decisive factor in the perceived quality of regional public health reporting in The Netherlands
[16]. Moreover, Bekker et al. described how informal interaction between researchers and
policy-makers during this process facilitates acceptance of research, using the concept of
backstage work introduced by Goffman [17, 18].
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Based on these findings, we decided to take into account the developmental process
and alignment between researchers and policy-makers to investigate the options for
strengthening the DHCPR contribution to policy-making. Contribution Mapping formulated
by Kok and Schuit provides a method to take into account the social context of a research
project [19, 20]. According to its Three Phase Model, researchers and policy-makers form
a hybrid during the co-creation of research, which consists of three phases (Figure 4.1):
formulation (activities to initiate the research process); production (activities to realize the
knowledge products); and extension (activities to make knowledge available to potential
users).
The phases can generate ‘contributions to action’, a concept which encompasses categories
such as ‘change in abilities and actions of involved and linked actors’, ‘contributed
knowledge products’, ‘contributions through linked utilization’ and ‘indications of utilization
at-a-distance’ [19]. Furthermore, contribution mapping recognizes the importance of
‘alignment efforts’. These are specific actions in the research process to enhance the desired
contributions of the research.
Figure 4.1. Three-phase model by Kok and Schuit [19].
Our aim was to study the development of the 2010 DHCPR to identify which areas need
specific alignment efforts by researchers and/or policy-makers to enhance the Report’s
contribution to policy-making [19].
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Method
A qualitative case study including document analysis (records of the DHCPR process and
policy documents) and interviews [21]. In the semi-structured interviews, we used a
deductive topic list based on the theoretical framework and structured according to the
Three-Phase Process Model (Supplementary File I). An independent researcher (not
employed by RIVM) interviewed: eligible researchers of the RIVM project team (3 project
leaders and 5 researchers); and nine senior policy makers from different MoH directorates
were members of the Ministry’s project group. One additional policy-maker responded by
e-mail.
First, four informal interviews were conducted to explore the DHCPR context. The other 13
interviewees were selected on the basis they had participated in the project group for both
the 2010 and 2014 Reports and/or because they were referred to in the informal interviews.
During the interview period, the 2014 Report was being prepared so we included topics to
investigate whether any changes had been implemented since 2010. Each interview lasted
approximately 60 minutes, was recorded and transcribed verbatim. After importing the data
into Atlas-ti version 7.0, the data were coded according to a deductive code list that was
inductively completed (Supplementary file II). The coding of the interviews started while
data collection was still ongoing. Three researchers independently coded two interviews
and we validated the coding list in a joint session to reach consensus. We reconstructed
the DHCPR2010 process and analyzed the alignment efforts and contributions. We also
performed a member check.
Results
We present our findings by describing noticeable issues for both the contributions of the
2010 Report to policy-making and the alignment efforts during the developmental process
of the DHCPR 2010.
Contributions
Position as information source for policy-makers
The unique selling point of the DHCPR is that it offers an overall picture of the health care
system. This makes it useful for policy directorates and policy-makers who deal with the
health system at a macro level (such as the policy directorate for Market and Consumer
and higher MoH levels). Policy-makers dealing with more specific health domains (such as
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long-term care or health care insurance) mentioned that, for their directorates, the DHCPR
merely adds to more detailed information from other sources. For them, the DHCPR was
not the distinctive and indispensable information source intended by RIVM. One policy-
maker stated that ‘It is a good product, but as basis for policy-making, it is too broad.’ They
considered the content was too general and the data outdated and preferred the original
(and more up-to-date) data of other sources.
In the light of policy-making dynamics, such as a change of government and the need for
political responses to today’s problems, researchers indicated that strategic timing of DHCPR
is almost impossible. The production period of such a major report is long (now even four
years) and inflexible which makes it difficult to attune to the policy-making cycle.
New communication tools
After the publication of the 2010 Report, RIVM launched a website to improve the accessibility
and topicality of DHCPR data. This publicly accessible website allowed for interim updating,
which proved to be an important reason for the MoH to delay commissioning the next
edition until 2014. Based on website visit numbers, the researchers expected the DMCPR
to have an increased contribution to policy-making. As one researcher mentioned ‘…an
update generates a peak, there are more visits; apparently it is noticed.’ However, interim
website updates depended on availability of new data, making these updates somewhat
arbitrary. Although policy-makers were positive about the update feature, they did not
think that the website contributed to an increase of their DHCPR use, some indicated that
the interrelationship between the trends and conclusions described in the DHCPR and the
randomly updated website was not clear.
In 2012, RIVM intended to renew public attention for the DHCPR in a novel way by publishing
infographics based on already published data. The first infographic on health care costs
generated substantial social media attention and increased visits to the DHCPR website.
Before publication, RIVM did not feel the need for extensive alignment on content and
timing with the MoH. Policy-makers assessed the infographic’s contributions and considered
the infographic particularly informative for the public but not relevant for themselves. Some
were not familiar with the infographic, while other policy-makers entered into a debate with
RIVM because figures presented in the infographic seemed inconsistent with a ministerial
report that was published on the same day. These policy-makers were concerned that any
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inconsistency between definitions used in the infographic and the ministerial report could
give political trouble. In this context, one policy-maker stated ‘… at least send it first to the
MPG so that we can check the figures, (....) and align the timing’ whereas a researcher
argued ‘It (infographic) contained nothing new, but now you make a graphic of it, they
(policy-makers) suddenly notice things they didn’t notice before.’
Importance as international business card
An additional function of the DHCPR is that of ‘international business card’. Due to its
translation into English, it can serve as a comprehensive description of the Dutch health care
system. Dissemination of the English version contributed to the RIVM researchers’ position
in the international scientific community. In contrast, most policy-makers did not value this
DHCPR function as highly, though it contributed in a practical way to their work by showing
the performance of the Dutch health care system internationally:
‘It (DHCPR) is pretty good for our public relations; internationally it is also valued. (……).
However, if you really look at its impact in the sense of ‘what is its influence on policy and
changes’, it is rather limited.’
Response to research agenda
In every edition of the DHCPR, the RIVM researchers have dedicated one chapter to
knowledge gaps and lacking data on measuring health care system performance, which they
consider a research agenda. Despite this, generation of useful and acceptable qualitative
acceptable data remained a source of concern. So far, the DHCPR project itself had only the
task and budget to collect and integrate data. In 2012, RIVM made a strategic analysis on
data supply for DHCPR and concluded that data on public health and health care require but
lack strategic direction [22]. However, RIVM is not in a position to direct data generation by
other parties. The policy-makers recognized the issue but considered data generation the
responsibility of health care organizations. Nevertheless, some expressed the intention to
improve information management in the health care system, together with RIVM, in the
near future.
Alignment efforts in the DHCPR 2010 process
Aim of DHCPR: choice of indicators
Based on a theoretical framework, RIVM had established the performance indicators for the
first 2006 edition of DHCPR in an interactive process with policy-makers and academics [1,
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23]. To enable long term monitoring, the indicator selection remained almost unchanged
over the years. For the 2010 edition, the aim of DHCPR was not discussed in the formulation
phase. Only some slight adaptations were made to the indicator set and definitions. However,
we noticed that policy-makers differed in their opinion on the intended users and the choice
of indicators: ‘In fact, all directorates at the Ministry belong to the DHCPR target group.’; ‘In
my opinion, (the intended DHCPR user is) not our Directorate’; ‘Maybe policy-makers should
not be the intended users of this booklet, but people interested in health policy.’
Some members of the MPG changed over the years and for the 2010 edition, the group
included members who had not been involved in 2004. After the 2008 Report, RIVM
had conducted a survey of policy-makers to investigate which indicators they considered
important. Due to the varied results, RIVM decided to stick to the existing indicators.
However, the discussion on appropriate indicators reappeared for the 2010 Report during
the production phase causing divergence of opinion between RIVM and some policy-makers:
‘Several times, we indicated that we preferred other indicators and that those (selected) did
not give a full picture of our policy. (…..) Nevertheless, at a certain moment, RIVM made their
own choice to include these indicators.’
Backstage work: regular meetings and participation in the project group
During the production phase, the RIVM project team had regular meetings with the
Ministry’s project group to discuss progress, methods, indicators and drafts for the DHCPR.
Furthermore, the project leaders had weekly telephone calls with their contact person at
the MoH. Due to these alignment efforts, the Ministry project group members were familiar
with the DHCPR content before release. The RIVM researchers were dedicated to find data
for indicators and to integrate their findings in draft texts. They had incidental interaction
with the project group or individual policy-makers and gained a limited view on the policy-
making dynamics at the MoH.
Each MoH directorate appointed a project group member, mostly senior policy-makers with
a broad overview of their field. The members’ involvement in the group varied according to
their policy domain and personal interest: ‘We intentionally composed a project group where
people from different directorates (…) could give input. Largely, it (active participation) then
also depends on the person.’
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For the Ministry project group, the final episode of the production phase was the most
lively when they discussed the formulation of the final report with the RIVM project leaders:
‘That is the fascinating ‘game of words’ that you play; how are you going to formulate (the
conclusions) in such a way that we both agree with it.’
Policy-makers particularly focused on checking data relevant for their own directorate to
verify consistency with other data used by the MoH. For them, preventing political turmoil
was an important objective.
Double role actor: important alignment effort discontinued
To pave the way, one project leader had his office at the MoH and maintained a large informal
network of policy-makers which enabled him to identify upcoming policy issues and the
policy-makers’ needs. If policy-makers had questions with respect to the DHCPR, he could
rapidly provide them with an answer. In the interviews, both researchers and policy-makers
stressed that this confidence-building double role was beneficial for the DHCPR process.
In 2010, the person in this double role retired and his position remained unfilled during
the development of the 2014 Report. This was regretted by colleagues and policy-makers:
‘He knew what was going on and who to contact for what. That (retirement) might be a
disadvantage in comparison with previous (DHCPR) processes’.
Extension strategy: gaining ongoing attention for DHCPR
The extension phase started with the release of the Report in 2010 and was going to last for
four years instead of two, due to the extended period between editions. After the formal
presentation to the Minister of Health, the RIVM project team also presented the report to
a wide audience of policy-makers at a well-attended meeting and disseminated hard copies
to the MoH. Dissemination by Ministry project group members in their own department
depended on their interest in the DHCPR, reflecting their position in the group during
the production phase. One policy-maker described her routine as: ‘I send an e-mail like
‘colleagues, this is the publication’ and I also mention that anyone interested could collect a
hard copy at my room. So, I do communicate that a DHCPR is published.’
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After this initial period, policy-makers’ attention evaporated quickly in the continuous
information overload. As one policy-maker said: ‘Every day, reports arrive and you can be
unlucky that it coincides with something else (….). It is very hard to ‘time’ those things.’
The RIVM project team recognized the need for continuous efforts to gain attention for the
Report during the extended four year period to 2014. They applied new communication
tools (website, infographics) to reach policy-makers after publication, as recommended
in the evaluation report on the 2008 Report [14]. The regularly updated website did not
automatically gain the attention of policy-makers. As one of them stated: ’I guess that these
(updates website) are certainly interesting for colleagues, but they have to know about it
and should not forget it (…). They have to campaign for that.’
Discussion
Opportunities for improving alignment
Alignment with differing policy-makers
RIVM researchers tended to consider the key users of the DHCPR as one group, ‘the policy-
makers at MoH’. Although this may be apparently true from a distance, different needs in
each policy domain existed. To get round interpretation barriers, a watchful attitude with an
eye for policy-makers’ perspectives is indispensable [15]. Some policy-makers felt ignored
because indicators they proposed were not included in the Report. Although the RIVM
project team considered this mismatch inevitable due to the macro level, it nevertheless
adversely influenced the DHCPR image at the MoH. Alignment with policy-makers,
specifically those newly involved, to create acceptance of choices requires continuous
attention during the production process. The project team could develop the backstage
work with direct involvement of researchers, to improve the Report’s alignment with policy
in the early production phase [24].
Alignment in language
Whereas RIVM researchers hoped for discussions with policy-makers on the impact of their
findings, the language used to describe findings turned out to be more important for policy-
makers. Specifically the way RIVM formulated their findings on the (not yet) achieved policy
goals, was of major concern. Policy-makers quite often explained their concern by saying
‘you may equally well write down ‘the glass is half-full’ as write down ‘the glass is half-
empty’’. The policy-makers were concerned that the Report did not present achievements
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as ‘half-empty’. The boundary between science and policy had to be negotiated. This
was primarily done in the interaction between project leaders and policy-makers in the
backstage. Involving other researchers directly in backstage work can create more feeling
for the impact of language which could improve the presentation of findings.
Alignment by person adopting a double role
A researcher, who is part-time positioned at the MoH and can take the lead in efficient
alignment with policy-makers at the MoH, is regarded as a major alignment effort by Kok
& Schuit [19]. The development of the DHCPR had such a person in a double role and his
contribution to alignment was widely recognized. Despite this, the double role was not filled
for the development of the DHCPR in 2014 and a valuable alignment effort imperceptibly
disappeared.
Alignment with knowledge products from other sources
Policy-makers compared the DHCPR with reports and information from other sources, which
influenced how they valued DHCPR. More alignment with other sources on areas of special
interest and timing of products could strengthen the DHCPR position in the information
flood that policy-makers face.
Alignment on data management
Both policy-makers and researchers felt rather powerless with respect to tackling the data
gap that frustrates filling of indicators with recent figures. Data management is of vital
importance and needs a strategic approach [22]. On this issue, higher management levels
should be involved to create better prospects.
Alignment on the function of products
RIVM initiated two new presentation forms to bring the Report to the policy-makers’
attention – a regularly updated website and infographics. Not all policy-makers were
automatically receptive to these spin-off products. The website’s updates attracted limited
attention while the first infographic remained unnoticed and caused some concern about
the publication of consistent figures. Because the relation between the different DHCPR
presentation forms remained unclear for the policy-makers, they were not convinced about
the usefulness of the new products. Timely alignment on presentation forms and product
coherence are important for policy-makers.
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Methodological reflections
We used contribution mapping to analyze retrospectively how alignment efforts played
a role in understanding the contributions the Report made to health policy-making. We
used the Three Phase Model to structure the topic list and explained it to the respondents,
combined with the DHCPR development chronology. Although the phases were less distinct
in reality, the model enhanced the respondents’ recollection of the process and proved to
be useful.
Policy-making is a complex process in which many factors are important and linear knowledge
use is secondary [11]. Contribution mapping unraveled leads for better alignment in the
future. Although this method offers an example of nine alignment efforts, it does not restrict
alignment efforts and we were enabled to formulate our own specific areas for alignment
efforts.
An additional benefit of contribution mapping is that the method turned out to be an
alignment effort in itself, initiating discussion between the project leaders of RIVM and
MoH. We informed them on the findings by an extended study report and also put effort
in securing our findings for the RIVM organization by designing a tool for RIVM researchers
to help them to reflect on the research process. Currently, this tool is under development.
Study limitations
Our insights relate to interaction at project level, since we restricted the respondents to
RIVM researchers and directly involved policy-makers. It could be beneficial to conduct
research on the influence of the wider organizational context, as contributions could follow
indirect pathways and alignment at management level also may generate improvement.
Moreover, interviewees may not have fully remembered all relevant information or have
suffered from recollection bias. However, minutes of meetings were consulted, and served
as a triangulation tool for the interviews. The number of interviewees was large enough to
get a general picture of how the process was executed.
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Conclusion
We identified six areas where specific alignment efforts could help to improve the
contribution of future DHCPR editions to policy-making. These are efforts to:
• include balanced information for all relevant ministerial directorates;
• enhance the participation and commitment of policy-makers and researchers in
backstage work;
• blur the boundaries with the policy-making world by assigning people with double
roles;
• align with relevant reports from other sources;
• approach strategically data collection and enhance data generation for lacking DHCPR
indicators; and
• align the presentation of different DHCPR functions and products with the user’s
needs.
Establishment of structured alignment efforts is just the first step. On the long term, they
need attention, evaluation and maintenance. Due to the repetitive character of the DHCPR,
the definition of a new edition may become routine and minimal alignment efforts could
seem enough in the formulation phase. The pitfall is that this may result in divergent,
implicit expectations and a blurred DHCPR definition. Project groups where researchers and
policy-makers meet to discuss the progress of the DHCPR were important but are not a
guarantee for sufficient alignment with all policy-makers because the Ministry consists of
different policy worlds with their own goals and own policy logic. One valuable alignment
effort, the person with a double role, could disappear unnoticed if not recognized as an
organizational asset.
The contribution of health care performance reporting to policy-making is complex and
requires intensive alignment efforts. Not only is the number of alignment efforts important
but also their frequency. Researchers and policy-makers should undertake continuous
alignment efforts during all phases. Furthermore, both should reflect on existing alignment
efforts and regularly analyze the outcome to adapt to changing circumstances. Although
implementing alignment efforts may demand considerable resources, this investment is
worth considering since it will pay back in better contributions to health care policy-making.
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2. Dutch Health Care Performance Report 2006 [Zorgbalans. De prestaties van de Nederlandse gezondheidszorg in 2004]. In: Westert GP, Verkleij H., editors. RIVM rapport 260602002. Bilthoven: RIVM; 2006.
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4. Westert G, Van den Berg M, Zwakhals S, Heijink R, De Jong J, Verkleij H. Dutch Healthcare Performance Report 2010. Bilthoven: RIVM, 2010.
5. Weiss CH. Policy research: data, ideas or arguments? In:Wagner P,Weiss CHW,WittrockB,Wollman H, editors. Social sciences and modern states. Cambridge: Cambridge University Press; 1991. p. 307–332.
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9. Bekkers V, Fenger M, Homburg V and Putters K. Doorwerking van strategische beleidsadvisering. 2004. Available from: http://hdl.handle.net/1765/1594. Accessed 2013.
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13. Lomas J. Connecting research and policy. Isuma: Can J Policy Research. 2000;1(1): 140-144.14. Bouwman RJR. Research utilization in policy making. The utilization of the Dutch Health Care
Performance Report (Zorgbalans) in governmental policy making. Master Thesis. Bilthoven: RIVM; 2010.
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Supplemental material
The online files are available at http://hsr.sagepub.com/supplemental
Chapter 5
Contributions of knowledge products to health policy:
a case study on the Public Health Status and Forecasts
Report 2010
Published: European Journal of Public Health 2016. 2016; 26(6):922-927
Ingrid Hegger
Maarten O. Kok
Susan W.J. Janssen
Albertine J. Schuit
Hans A.M. van Oers
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Abstract
Background
The Dutch Public Health Status and Forecasts report (PHSF Report) integrates research data
and identifies future trends affecting public health in the Netherlands. To investigate how
PHSF contributions to health policy can be enhanced, we analysed the development process
whereby the PHSF Report for 2010 was produced (PHSF-2010).
Method
To collect data, a case study approach was used along the lines of Contribution Mapping
including analysis of documents from the PHSF-2010 process and interviews with actors
involved. All interviews were recorded and transcribed ad verbatim and coded using an
inductive code list.
Results
The PHSF-2010 process included activities aimed at alignment between researchers and
policy-makers, such as informal meetings. However, we identified three issues that are
easily overlooked in knowledge development, but provide suggestions for enhancing
contributions: awareness of divergent; continuously changing actor scenarios; vertical
alignment within organizations involved and careful timing of draft products to create early
adopters.
Conclusion
To enhance the contributions made by an established public health report, such as the PHSF
Report, it is insufficient to raise the awareness of potential users. The knowledge product
must be geared to policy-makers’ needs and must be introduced into the scenarios of
actors who may be less familiar. The demand for knowledge product adaptations has to
be considered. This requires continuous alignment efforts in all directions: horizontal and
vertical, external and internal. The findings of this study may be useful to researchers who
aim to enhance the contributions of their knowledge products to health policy.
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Introduction
Public health status and forecasts report
The Dutch National Institute for Public Health and the Environment (Rijksinstituut voor
Volksgezondheid en Milieu, RIVM) has published a Public Health Status and Forecasts Report
(PHSF Report) every four years since 1993, most recently in 2014 [1]. The PHSF Report
integrates research data on public health and identifies future trends in public health in the
Netherlands.
Since the first edition, both the format and the focus of the PHSF report have changed
repeatedly, reflecting developments in public health. An important moment in PHSF history
was the establishment of its official status in the policy cycle by the Dutch Public Health Act
(Wet Publieke gezondheid) in 2002. The PHSF Report provides the policy themes for the next
step in this cycle: the publication of the ‘National Health Memorandum’ by the Public Health
department on behalf of the Minister of Health [2]. (figure 5.1)
RIVM: Public Health Status
and Forecasting (PHSF)
Ministry of Health: National Health Memorandum
Municipalities: Local PHSF and local
memoranda
Health Care Inspectorate:
‘State of Health Care’
Figure 5.1 Public Health Policy Cycle in The Netherlands. The PHSF Report provides the policy themes for the National Health Memorandum of the Minister of Health by law. Local PHSF reports are the basis for health memoranda of the municipalities and are developed by Community Health Services in a comparable process as the national PHSF.
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Another interesting development is the translation of the national PHSF Report into local
PHSF Reports by Community Health Services since 2006, in line with the decentralization of
health care to municipality level in the Netherlands [3].
Despite its established use for the National Health Memorandum, improvement of PHSF
contributions to health policy-making is still an issue. It remains challenging to use the report
as effectively as possible. Both RIVM and the Ministry of Health (MoH), Welfare and Sport
want the PHSF Reports to serve as a knowledge base for policy-makers; not only for policy-
makers of the PH department acting as the principal, but also for policy-makers of other
MoH departments. For this study, we formulated the following research question: What
improvements need to be made to the PHSF process in order to enhance PHSF contributions
tonationalhealthpolicyinthebroadsense?
Theoretical background
Science-policy relations have been described in a variety of theoretical models. Traditional
‘positivist’ models of knowledge utilization emphasize the importance of bridging the gap
between the policy-making and research domains. Weiss’ typology of knowledge use in
health policy contributed to awareness of the possible functions of knowledge products
in policy-making; as a source of data, ideas or arguments.4 An important notion is that
knowledge uptake is not as rational as is often assumed. In practice, policy-making is
incremental in nature and is a highly complicated process involving many actors and levels
of government. Theories on the complex policy process can help scientists who want to
contribute to policy-making to understand the role of knowledge in that process [5-8]. To
address this complexity, interaction models for knowledge use have been developed that
take into account the policy-makers’ needs and that focus on the interaction between
researchers and policy-makers, as reflected in the model developed by De Goede, e.g. [9].
The ‘constructivist’ perspective goes a step further by considering knowledge as a social
construct produced in a co-creation process [10, 11].
PHSF process
The PHSF Report has been described as an example of a successful ‘boundary object’
developed through co-creation and connecting the science and health policy domains,
while RIVM has been characterised as a ‘boundary organization’ in Guston’s terminology
[11, 12]. A range of actors participate in the PHSF process, including RIVM scientists, policy-
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makers and scientists working in academia. RIVM scientists repeatedly interact with policy-
makers in the PHSF Policy Advisory Group (PAG) during the development process. Increasing
attention was devoted to alignment with stakeholders in successive PHSF processes. In her
analysis of the PHSF Report as a boundary object, Van Egmond has pointed out the role of
the PAG as a ‘backstage area’ where negotiations about the boundaries between science
and policy-making take place [13]. According to Goffman’s concept of ‘backstage work’ vs.
‘front stage presentation’, these informal negotiations enable the creation of an aligned
knowledge product that is acceptable to both the commissioning client and the research
organization and that can be officially presented to the outside world on ‘the front stage’
[14].
Study approach
To complement the already existing insights, we intended to develop practical
recommendations for researchers to improve the contributions made by the PHSF Report.
De Leeuw has observed that ‘current perspectives (both Knowledge Translation and the
Actor-Network Theory) do not reflect appropriately on actions that can be taken at the
nexus between research, policy and practice in order to facilitate more integration’ [15].
Kok and Schuit have developed the Contribution Mapping (CM) approach for analyzing
‘how’ knowledge is converted into action [16]. Kok and Schuit took the complexity of
knowledge production into account and conceptualized knowledge utilization as so-called
‘contributions to action’. A contribution is made when knowledge is included in the ‘actor
scenario’, representing the actor’s view of the future. Specific actions—so-called ‘alignment
efforts’—can be undertaken to align with the relevant actor scenarios and to enhance
the contributions of knowledge. To facilitate the analysis of alignment efforts, CM uses a
three-phase model of knowledge production: a formulation phase to define the research
question and approach, a production phase to conduct research, and an extension phase to
disseminate the research results [16]. (figure 5.2)
By using the CM approach to analyse the PHSF-2010 process, we expected to gain detailed
insights for the identification of areas that specifically require alignment efforts.
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Figure 5.2 Three-Phase Model by Kok and Schuit [16]. In the three-phase process model, investigators and linked actors interact during the research process. During the process, contributions to health policy can already be realized. The process narrows when the research approach is decided on. In the production phase, the process narrows again as knowledge products are realized. In the extension phase, the knowledge is disseminated [16]. Published before in reference [16].
Methods
To collect data on the PHSF-2010 process, we used a case study approach that included
analysis of documents related to the PHSF-2010 process and in-depth semi-structured
interviews with involved key actors at both RIVM and MoH who were able to survey
the process at different organizational levels [17]. Two RIVM researchers conducted the
interviews with RIVM experts and managers involved in the PHSF-2010 process in 2011 (n
=10).An independent researcher (notworking at RIVM) conducted the interviewswith
policy-makers and managers at the MoH in 2013 (n =10).All interviewswereconducted
using a list of topics based on the theoretical framework (Supplementary Materials), and
were recorded and transcribed ad verbatim. We coded the interviews in the Atlas-ti 7.1.3
software package using a deductive code list that was based on the theoretical framework
and inductively supplemented based on extensive and iterative analysis of the interviews.
In an open coding session, three researchers discussed the coding of two interviews
until consensus was reached. We identified areas for alignment efforts using a constant
comparative analysis method [18].
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We operationalized the CM concepts as follows:
1. ‘Actor scenario’: actor’s view of health policy future and/or his/her professional
future
2. ‘Alignment efforts’: opportunities for actions taken by RIVM scientists, policy-
makers and managers of both RIVM and MoH to align the PHSF-2010 Report with
the needs of the MoH
3. ‘Knowledge’: the integration of research data on public health for the purpose
of the PHSF-2010 Report, the PHSF-2010 Reports (knowledge products), and the
exchange of knowledge through interaction between actors
4. ‘Contribution (to action)’: any indication that PHSF knowledge was included in an
actor scenario
5. ‘Formulation phase’: period for defining the PHSF-2010 scope (2006–7)
6. ‘Production phase’: period between agreement on the PHSF- 2010 scope and the
publication of the PHSF-2010 reports (2008–10)
7. ‘Extension phase’: period after publication in 2010, evaluated until 2013
Results
Alignment in the formulation phase
In the Formulation Phase, RIVM aligned with the policy-makers of the Public Health
department about the course to take and agreed to develop a main report and four thematic
reports, all to be delivered in 2010.
Until 2006, the PHSF Report was mainly used by the PH department. Both RIVM and PH
policy-makers expected that co-financing by other departments would be favourable for
involving them more directly in the PHSF process and strengthening PHSF contributions in
the broader health policy domain. For the first time, the Macroeconomic Issues and Labour
Market Department (MILM) provided a budget that was used to develop a thematic report
on the societal benefits of health care [19].
Alignment in the production phase
Once the Production Phase started, the PAG was formed with senior policy-makers of the
relevant MoH departments. (figure 5.3)
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The RIVM project managers regularly consulted the PAG and experienced that different
departments had varying views and needs. The PH director, who also served as the PAG chair,
challenged RIVM to describe implications for health policy. His opinion was that facts need
interpretation to contribute to policy-making: ‘If RIVM only publishes reports that provide
facts, but do not reflect upon the implications, the policy impact of the document will be
zero and it will be ignored. So it needs to provide a trigger... that is the art of balancing, you
should not cross the line, but you have to provide a trigger and ensure that the message is
not lost.’
However, MILM policy-makers appeared not to be in favour of near-to-policy statements by
RIVM and as new co-financier, they interfered in discussions about the content of the PHSF-
2010 Report. For example, the interpretation of socio-economic health inequalities (SEHIs),
a highly political issue, appeared to be controversial. As one policy-maker mentioned:
‘I argued over that issue (the draft text on SEHIs) with X (RIVM researcher) by phone, since I
believed that the text contained too many political opinions.’
Minister of Health, Welfare and Sport
State Secretary for Health, Welfare and Sport
Directorate General of Public Health Directorate General of Curative
CareDirectorate General of Long-
term Care
Sports Department
Public Health Department (PH)
Healthcare Disciplinary Boards Secretariat Unit (EST)
Secure Youth Care Implementation Unit (UGJ)
Curative Care Department
Pharmaceuticals and Medical Technology Department
Market and Consumer Affairs Department
Long-Term Care Department
Social Support Department
Health Insurance Department
Department represented in the Policy Advisory Group of PHSF-2010
Macroeconomic Issues and Labour Market Department (MILM)
Advisory and support departments
Secretary GeneralDeputy Secretary General
Nutrition, Health Protection and Prevention Department
Figure 5.3 Organization Chart of the MoH, Welfare and Sport in the Netherlands. The departments indicated in italic underlined characters were represented in the PAG of the PHSF-2010 process.
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Due to time constraints, the thematic reports were completed at the last minute just before
the strict deadlines. The PAG members had hardly any time to read the drafts, hindering
discussion on the content. According to a PAG member, this resulted in a missed opportunity
for alignment: ‘We finally received the thematic reports, which contained hundreds of
pages, at the last minute. In the first place, this gave us the feeling that we could not make
any changes or recommendations, since the process was already completed and the reports
were already finished. In the second place, this also influenced the impact of the thematic
reports later on (....). If the PAG members, the ‘early adopters’, discuss the reports, then it will
sink in properly and that will lead to further dissemination.’ Timely delivery of knowledge
products is a well-known factor for successful contributions. Although the PHSF-2010 Report
was completed in time, we found that timely draft versions are also important to take full
advantage of backstage opportunities in order to create support and enhance contributions.
RIVM professionals recognized that familiarity with the MoH organization is important for
successful alignment. As one researcher said: ‘I think you need to know how things work at
the Ministry of Health. You need to know what they are dealing with. You need to understand
their issues, without fully identifying with them.’ One respondent left RIVM and joined the
Ministry of Health and found out that he did not know the Ministry as well as he thought he
did: ‘When I worked at RIVM, I thought I knew how things worked (at the Ministry). However,
when I myself was employed by the Ministry for four-and-a-half years, I discovered that in
fact I knew very little about it. (...) I had never realized that before, because at RIVM I was
one of the few people who maintained very close contacts with the Ministry. People thought
I knew what went on there.’ This finding underlines the need for continuous attention to
evolving actor-scenarios and policy-makers’ needs.
Another important finding was that effective alignment requires consistent alignment
efforts at every hierarchic level, as well as conscious vertical alignment within the
involved organizations. Since the PHSF is the formal starting point for the National Health
Memorandum, alignment at all hierarchical levels between RIVM and MoH should be a
matter of course. However, coordination was lacking due to limited internal alignment. The
RIVM project managers acted independently in line with the RIVM matrix structure, while
senior management remained distant.
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Alignment in the extension phase
The ‘front stage’ presentation of the PHSF Report to the Minister took place at an event
where the Health Care Inspectorate’s ‘Staat van de Gezondheidszorg 2010’ Report (State of
Health Care-2010) was also presented. Immediately afterwards, senior RIVM management
misrepresented the PHSF-2010 message to the press by confusing it with the Inspectorate’s
message. This was caused by insufficient familiarity with the PHSF-2010 content as a
result of lacking vertical alignment. Articles appeared in the press claiming that the report
had recommended ‘strong government measures to promote a healthy lifestyle’, and
had concluded that ‘many preventive health campaigns are ineffective’. These messages
conflicted with the intended optimistic PHSF-2010 messages as aligned with the MoH.
The media reports caused inconvenience for MoH policy-makers and they experienced
difficulties in obtaining funding for preventive campaigns for some time. One policy-maker
complained: ‘There was no attention paid to the PHSF messages and for about six months to
a year, we had to repair the situation with Parliament.’
After publication, the focus at the MoH quickly shifted from the PHSF Report to the issues
of the day. Alignment during the production phase is regarded as important for early
knowledge transfer and the creation of ‘early adopters’. However, many of the key actors
(coincidentally) changed in the PHSF-2010 extension phase. This included several PAG
representatives, the PHSF project managers and senior managers (both at RIVM and MoH).
Their successors were less involved in the PHSF-2010 process or not involved at all, which
illustrates the ongoing need for alignment efforts in the extension phase although hardly
any budget was available for these activities. As one policy-maker put it: ‘RIVM should work
together with the PAG and should carefully examine how best to promote the PHSF Report
both within and outside the MoH after the report’s presentation. We should remind people
where and how to find the report, and how it might be valuable to them.’
Contributions to policy-making
The PHSF-2010 Report made a key contribution to the National Health Memorandum
published in 2011 [2], and both PH policy-makers and RIVM project managers were very
pleased with this. As one project leader put it: ‘I am pleased with the contribution to the
Memorandum. Of course, there are always points for improvement. However, the basic
PHSF-2010 issues and ideas were included.’
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The PHSF-2010 contributions to other health policy domains were less self-evident than
RIVM expected. Some PAG members indicated that they personally appreciated the PHSF-
2010 Report for the overall picture it provided of the public health situation, but that their
department needed information the PHSF-2010 Report did not offer, such as more specific
figures and facts. One policy-maker said: ‘They (RIVM) have all sorts of products and are very
supply-oriented. It’s as if they want to draw attention to their allegedly amazing products
without really knowing who they are talking to. To put it frankly, they imply that you would
be stupid not to use their data and products. However, in my view, you have to approach it
the other way round. I don’t have to use those products at all. I just need access to the right
information, and their task is to help me in whatever way possible.’ Researchers must realize
that actors have their own actor scenarios which may have implications for the process,
the concept, and the format of the knowledge to be produced. This again underlines the
importance of thorough familiarity with the target group, which requires a combination of
horizontal and vertical alignment efforts.
Discussion
Study limitations
Because the interviews were conducted in retrospect, recollection bias may have played a
role. However, we noted that the interview structure and the Three-Phase Model facilitated
recollection. Furthermore, documents, such as minutes of PAG meetings and the PHSF-2010
evaluation report were used for triangulation purposes in combination with the interviews.
The number of interviewees and the representation of all hierarchical levels amongst
respondents were sufficient to gain a good overview of the research process.
Reflections on the CM approach
We used CM to analyze how alignment influenced the PHSF Report’s contributions to health
policy-making. The analysis required a lot of time, making it unfeasible for routine evaluation
of research projects. However, we gained useful insights that are generally applicable, both
in our own organization and in other comparable knowledge institutes. We secured our
findings for the RIVM organization by designing a tool to support researchers in reflecting
on the research process, taking into account the important areas for alignment efforts. A
research article on this tool is currently being prepared.
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Conclusions
The analysis of the PHSF-2010 process using the CM approach produced several
recommendations for improving the contributions of the PHSF Report to health policy-
making. The PHSF-2010 process included intensive alignment efforts, such as interaction in
PAG meetings. However, we noticed three issues that need careful and specific alignment
efforts:
Actors and their own needs: organizational environment
To be able to decide what needs to be done to enhance contributions, researchers must
explore the actor scenarios of key actors. Since individuals can have a major impact and
actors change all the time, the analysis has to be updated on a regular basis to make sure
new scenarios are included.
Involvement of all hierarchical levels: vertical alignment
To steer the process in the right direction and to create the support needed, monitoring
of adequate vertical alignment is essential. We already noticed this issue in two other
case studies and it is clearly an ongoing challenge to manage vertical alignment for large,
hierarchical organizations like RIVM and MoH [20, 21].
Creation of early adopters: timing of draft products
Policy-makers need sufficient opportunities to comment on draft knowledge products to
enable them to become ‘early adopters’. This requires thorough process management and
researchers should consider spending part of their research budget for this purpose.
Regular actor scenario analyses, ongoing vertical alignment and timely draft products are
issues not exclusively related to the PHSF-2010 process, but also generally applicable to
the process of many other reports for policy support; also at other governance levels and
even in other countries. The general lesson to be learned from this study is that it is not
enough to raise awareness of a well-established knowledge product in order to enhance
its contributions to policy-making. This requires also regular exploration of the actor
scenarios of (sometimes less familiar) actors, and consideration of necessary knowledge
product adaptations. And in turn, this process will require alignment efforts in all directions:
horizontal and vertical, external and internal.
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Health Res Policy Syst. 2014;12:55.9. DeGoedeJ,PuttersK,vanderGrintenT,vanOersHA.Knowledgeinprocess?Exploringbarriers
between epidemiological research and local health policy development. Health Res Policy Syst 2010;8:26.
10. Wehrens R. Beyond two communities-from research utilization and knowledge translation to co-production?PublicHealth 2014;128:545–551.
11. Bekker M, van Egmond S, Wehrens R, Putters K, Bal R. Linking research and policy in Dutch healthcare: infrastructure, innovations and impacts. Evid Policy 2010;6(2):237–253.
12. Guston DH. Boundary organizations in environmental policy and science: an introduction. Sci Technol Hum Values 2001;26:399–408.
13. Van Egmond S, Bekker M, Bal R, van der Grinten T. Connecting evidence and policy: bringing researchers and policy makers together for effective evidence-based health policy in the Netherlands: a case study. Evid Policy 2011;7:25–39.
14. Goffman E. The Presentation of Self in Everyday Life. London: Penguin; 1990.15. De Leeuw E, McNess A, Crisp B, Stagnitti K. Theoretical reflections on the nexus between
research, policy and practice. Crit Public Health 2008;18:5–20.16. Kok MO, Schuit AJ. Contribution mapping: a method for mapping the contribution of research
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Publications Inc, 2008.18. Pope C, Ziebland S, Mays N. Analysing qualitative data. Br Med J 2000;320:114–6.19. Post NAM, Zwakhals SLN, Polder JJ. Maatschappelijke baten. Deelrapport van de VTV 2010 Van
gezond naar beter (Social Benefits. Thematic Report of PHSF-2010 ’Towards better health’). RIVM Report. Bilthoven: RIVM, the Netherlands; 2010.
20. Hegger I, Janssen S, Keijsers J, et al. Analyzing the contributions of a government- commissioned research project: a case study. Health Res Policy Syst 2014;12:8.
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Supplementary data
Supplementary data are available at EURPUB online.
Chapter 6
ResearchforPolicy(R4P):Developmentofareflection
tool for researchers to improve knowledge utilization
Published: Implementation Science 2016; 11(133)
Ingrid Hegger
Lisanne K. Marks
Susan W.J. Janssen
Albertine J. Schuit
Jolanda F.M. Keijsers
Hans A.M. van Oers
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Abstract
Background
To improve knowledge utilization in policy-making, alignment between researchers and
policy-makers during knowledge production is essential, but difficult to maintain. In three
previously reported case studies, we extensively evaluated complex research projects
commissioned by policy-makers to investigate how alignment is achieved in a research
process and to discover ways to enhance knowledge contributions to health policy. In the
present study, we investigated how the findings of these three research projects could be
integrated into a practical tool for researchers to enhance their contribution to evidence-
based policy.
Methods
A cross-case analysis was conducted to integrate the findings of the evaluation of the three
research projects and to identify important alignment areas in these projects. By means of
an iterative process, we prepared a tool that includes reflection questions for researchers.
The “Research for Policy” tool was tested with input from the project managers of three
new research projects. Based on the findings, the final version of the Research for Policy
tool was prepared.
Results
By cross-case analysis of the three case studies, the following important alignment areas
were identified: the goal, quality, relevance, timing, and presentation of research, the
tasks and authorities of actors, the consultative structure and vertical alignment within
organizations, and the organizational environment. The project managers regarded the
Research for Policy tool as a useful checklist for addressing the important alignment areas in
a research project. Based on their feedback, the illustrative examples from the case studies
were added to the reflection questions. The project managers suggested making the tool
accessible not only to researchers but also to policy-makers. The format of the Research for
Policy tool was further adjusted to users’ needs by adding clickable links.
Conclusions
Alignment between research and policy-making requires continuous efforts and a clear
understanding of process issues in the research project. The Research for Policy tool offers
practical alignment guidance and facilitates reflection on process issues, which supports
researchers in aligning with policy-makers and in acting in a context-sensitive way.
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Background
Policy-making is a complex process, and the use of scientific knowledge in policy-making, also
referred to as knowledge utilization, is not self-evident [1–3]. Not surprisingly, researchers
want to know why the scientific knowledge uptake into policy-making is so difficult. For
over 40 years, extensive research has been conducted on knowledge utilization, which
resulted into several generations of theoretical models explaining barriers and facilitators
[4–7]. Oliver et al. have pointed out that despite extensive research on knowledge utilization
and many efforts to enhance scientific knowledge uptake in policy, barriers have been
persistently identified in the literature, whereas only “little empirical data analyzing the
processes and evidence use in policy is available” [8]. They argue that researchers should
focus on understanding policy-making processes, the types of evidence used by policy-
makers, and the relationship between research and policy-making.
The first step for scientists is to recognize the characteristics of politics, policy, and
policy-making. As Pielke describes, politics is the “process of bargaining, negotiation, and
compromise” to determine how resources are allocated and under what conditions, whereas
“policy” indicates “the commitment of a group to a particular course of action” aiming at
a desired outcome for solving a specific problem [1]. Policy-making is thus the process to
recognize the problem and to formulate, implement, and evaluate the particular course of
action needed to solve the problem. To understand which scientific knowledge may help
policy-makers and contribute to policy-making and how this can be achieved, scientists
have to acknowledge that policy-making is a dynamic, complex process in which different
sources of knowledge and information are used and where the values and interests of
various stakeholders have to be taken into account [7]. The components of the process, i.e.,
agenda setting of a problem, followed by formulation, implementation, and evaluation of
policy, are often represented as successive stages in a policy cycle. However, policy-making
is shown to be less linear and more iterative in practice [9–11]. In this complex process,
scientific knowledge may have an indirect, not clearly discernible role: besides instrumental
use in a direct and specific way to solve a particular problem, it may also have a conceptual
function as a source of ideas or a symbolic/agenda-setting function when it is used to take
an advocacy position [12–15]. Because of the dynamics of the policy-making process and
the different purposes for which scientific evidence is used, it is generally recognized that
formal and informal interactions between researchers and policy-makers play a key role in
the use of knowledge in policy-making [16]. The constructivist perspective on knowledge
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utilization even goes a step further. In this perspective, science is a social process during
which scientific evidence is co-created by researchers and other involved actors, including
policy-makers [17]. As Kok and Schuit argue, this constructivist model is helpful in blurring
the boundaries between research and policy-making and discovering ways to align research
with policy-making in order to enhance knowledge contributions to policy-making [17].
Policy and policy-making may relate to various decision-making levels (national, local,
governmental, or private). In this paper, the focus is on research for governmental policy-
making by officials of a ministry or other governmental organizations at a national level. For
scientists working in this context, the different perspectives on knowledge and the insights
on knowledge utilization are particularly relevant. An example of a knowledge institute
working for governmental organizations at national level is the National Institute for Public
Health and the Environment (RIVM), the national public health institute in the Netherlands.
RIVM conducts research and integrates knowledge in the field of public health, health care,
safety, and environmental protection for governmental commissioning organizations such
as the Ministry of Health, Welfare and Sport and the Healthcare Inspectorate [18]. RIVM
and its clients have arranged formalized procedures to ensure agreement on research
proposals, knowledge products, and timelines for commissioned projects. The knowledge
products are important for making RIVM knowledge accessible to the target audience.
They may take a variety of forms, such as reports, scientific papers, fact sheets, websites,
or databases. In the RIVM annual commissioning cycle, RIVM researchers, specifically the
project managers, consult the policy-makers at the commissioning organization. These
policy-makers are their counterparts for a particular research commission and discuss the
articulation of the knowledge question and formulation of the project plan. They have the
task to arrange regular meetings with the commissioning client’s account manager and to
gear their knowledge products to the commissioning client’s needs. RIVM management
regularly monitors the progress of research projects and the timely delivery of products.
Despite these efforts to interact and align with the commissioning organizations, RIVM
researchers have found that the contributions of their knowledge products to policy-making
are not as significant as they expected. At the same time, commissioning organizations still
indicate that they would like to be provided with knowledge products that are optimally
aligned to their specific needs.
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To investigate how alignment is reached and to discover ways of enhancing the contributions
of RIVM knowledge to policy-making, we conducted a research project with two stages.
In the first stage, we carried out three case studies, for which we used Contribution
Mapping developed by Kok and Schuit [17, 19]. The case studies have been reported in
three published scientific articles [20–22]. In the second stage of our research project, we
translated the findings of the case studies into practical guidance by developing a reflection
tool to support researchers in their alignment efforts. This second stage of the research is
the subject matter of this paper. To provide background, we first summarize the findings of
the first stage of our research project. We then continue with reporting the conduct and
findings of the second stage.
Summary stage 1: three case studies
In the first stage of the research (2011–2013), we extensively evaluated three multi-
annual RIVM research projects: “Development of Risk Model,” “Development of Dutch
Health Care Performance Report 2010,” and “Development of Dutch Public Health Status
and Forecasts Report 2010”. For each project, we analyzed the process in detail using the
Contribution Mapping approach [17]. Based on a constructivist perspective, Contribution
Mapping developed by Kok and Schuit is a method to evaluate the utilization and impact of
knowledge generated by research projects in health policy-making. The method enhances
the understanding of research processes and alignment between researchers and health
policy-makers. It is based on a three-phase model of the research process; a Formulation
Phase to define the research question and plan, a Production Phase to conduct research,
and an Extension Phase to disseminate the research results. (Figure 6.1)
Contribution Mapping conceptualizes the utilization and impact of knowledge through
so-called contributions to action: “Contributions are activities that enable the conversion
of knowledge into an element in decisions and implementation, a part of practices or a
component in innovation” [17]. We consider the concept contribution valuable since it
reflects that knowledge conversion into policy-making can take many, even very subtle,
shapes and forms, already during the research process. The more comprehensive concept
knowledge utilization may suggest that it is about the complete uptake of certain knowledge
in policy-making, which may disguise partial, but meaningful use. To contribute to the work
of actors, i.e., the persons or organizations involved, knowledge has to be included in the
so-called actor scenarios. These are (virtual) scripts implicitly or explicitly formulated by the
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actors representing their view of the future and their pursuit. Alignment is an important
concept in Contribution Mapping and means that research and policy-making are attuned
and this is reached by reciprocal interaction instead of a one-way interaction from research
to policy-making. To enhance the contributions of knowledge, alignment with actors and
their actor scenarios is necessary. Specific actions can be taken for this purpose, so-called
alignment efforts, defined by Kok and Schuit as “anticipatory efforts that aim to enhance
contributions” [17]. Both researchers and policy-makers can undertake alignment efforts.
Due to some push and pull in this process, both positions may move resulting in knowledge
and knowledge products (better) attuned to the needs of policy-makers and researchers.
Figure 6.1 Kok and Schuit’s three-phase model [17]
In each case study, we described the alignment efforts during the research process and the
contributions that the project made to the policy-making process [20–22]. An outline of the
three case studies is provided in Table 1 below. For further details, we refer to the research
articles on the case studies [20–22].
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Table 6.1 Outline of case studies
“Development of Risk Model” case study [20]This case study focused on the development of a risk-based approach for clinical trial inspections in the Netherlands and had to deliver risk models to enable ranking and stratified selection of clinical trials for inspection by the Dutch Health Care Inspectorate. These models had to contribute to the Inspectorate’s objective of using scientific knowledge for evidence-based supervision. We found that RIVM and the Inspectorate had divergent views on their collaboration and the ownership of the knowledge product, which resulted in different expectations. Researchers and commissioning inspectors were not aware of these different perceptions. We identified six relevant categories of both horizontal alignment efforts (between investigators and key users) and vertical alignment efforts (within RIVM and the Inspectorate organization) that affected the contributions to the Inspectorate’s work. Relevant alignment efforts became manifest at three levels: the first level directly concerned the project, the second level concerned the organizational environment, and the third level concerned the formal and historical relationship between the organizations.
Case study on Dutch Health Care Performance Report [22]The second case study concerned the Dutch Health Care Performance Report (DHCPR). The DHCPR is published by RIVM and commissioned by the Dutch Ministry of Health, Welfare and Sport in 2006, 2008, 2010, and 2014 [27]. Based on a scientific framework, the DHCPR monitors health care performance in the Netherlands by using indicators for quality, accessibility, and affordability. The aim of the report is to contribute to “strategic policy-making”. We identified six areas where alignment is specifically relevant for enhancing the contributions of future DHCPR editions: well-balanced information for different ministerial directorates, backstage work, double-role actors, reports published by other knowledge institutes, data collection and generation, and presentation formats.
Case study on Public Health Status and Forecasts Report [21]The third case study concerned the Dutch Public Health Status and Forecasts Report (PHSF), which integrates research data and identifies future trends in public health in the Netherlands [28]. The PHSF has a recognized function in connecting the science and policy domains because it is embedded in the national health policy cycle by law. The PHSF provides the policy themes for the National Health Memorandum (NHM), which is published every 4 years by the Minister of Health, Welfare and Sport. The PHSF2010 process included activities aimed at alignment between researchers and policy-makers, such as informal meetings. However, we identified three issues that are easily overlooked in knowledge production, but provide suggestions for enhancing contributions: awareness of divergent, continuously changing actor scenarios; vertical alignment within the organizations involved; and careful timing of draft products to create early adopters.
Purpose of this article
In the first stage of our research project, we used the Contribution Mapping method in three
case studies to gain insights into areas where specific alignment efforts can be helpful to
enhance contributions of RIVM knowledge and knowledge products.
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In the second stage, we translated the findings of the first stage by developing a tool to
support researchers in their everyday work, since the insights from the case studies did not
directly provide guidelines for improving alignment within future projects. The case studies
had shown that alignment between researchers and policy-makers is more difficult to
maintain in practice than expected. Moreover, the need for alignment efforts continuously
changes, depending on the research project and its current phase. We concluded that
the key to enhancing alignment efforts and therefore the contributions of research is the
researchers’ awareness of key alignment areas, combined with regular, systematic reflection.
This involves taking sufficient time to consider seriously the current situation of the project,
taking into account the alignment areas [20, 22].
We acknowledged that it would not be helpful to offer generic alignment efforts, since every
research project is different. Alignment efforts are difficult to predefine in a tool since they
depend on the specific research process (both the knowledge question and the project’s
context, i.e., the environment of the project that influences the process and outcome of
the project) at a certain point in time, making it impossible to suggest beforehand any
detailed (inter)actions applicable to each research project. Furthermore, we concluded
that the continuously changing context of research projects requires regular reflection
on the research process to identify the need for specific alignment efforts. We found that
researchers find it difficult to analyze regularly the process issues of their project, often due
to unawareness of important alignment issues, time constraints, and their preference for
scientific issues.
In this article, we report the results of the second stage of our research project. Firstly,
we describe how we integrated the findings of the three case studies of the first stage by
conducting a cross-case analysis. Secondly, we describe how we developed the Research for
Policy (R4P) reflection tool to support researchers in creating alignment with policy-makers
and preparing aligned knowledge products. For the formulation of the specifications of the
R4P tool, we took into account the insights acquired in the first stage. The process for the
development of the R4P tool is outlined in Fig. 2.
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Part A: Cross-case analyses
Methods
We systematically analyzed the alignment areas of the three cases as identified in the first
stage of our research project by a case-oriented approach [23]. In line with the Contribution
Mapping approach, we described the alignment areas in a table for comparison and drew
up a comprehensive list of important alignment areas [17, 19].
Results
The cross-case analysis of the three case studies revealed eight areas where deliberate
alignment efforts could specifically improve alignment between RIVM and the commissioning
Ministry of Health, Welfare and Sport (see Table 2). Based on the barriers indicated by de
Goede et al. and general alignment efforts formulated by Kok and Schuit, the alignment
areas “goal,” “quality,” “consultative structure,” “relevance and timing,” and “presentation”
were anticipated findings [16, 17]. The alignment areas “tasks and authority,” “vertical
alignment”, and “organizational environment” were additional areas.
Table 6.2 Consolidated list of areas for alignment
Area for alignment Topics
Goal The formulation of the knowledge question; exploration of its origin, the “question behind the question,” and the underlying need for the knowledge products
Tasks and authority The input of all involved actors (both researchers and policy-makers); their responsibilities, knowledge and data exchange by actors during the process, and the final authority over the knowledge products
Quality The research method; conceptual framework and data used in the research project
Consultative structure The consultative structure of the project; the sharing of relevant information and the relationships between actors; double-role actors
Vertical alignment Interaction within the organization conducting research and within the commissioning organization; interaction between hierarchical levels and the embedding of the project in the organizations
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Organizational environment The environment of the research project; awareness of relevant conditions external to the research project influencing the relationship between investigators and linked actors; incidents, media events, relationships with other organizations, changing priorities, and changing actors
Relevance and timing The formulation and wording of the research results and timing of the delivery and presentation of the knowledge products
Presentation The design and structure of knowledge products and the tools for the extension strategy
The alignment areas represent the topics where researchers should reflect on to achieve
sufficient alignment before and during the research project. In this way, they will be able to
determine whether they should put more effort into alignment.
• Alignment area Goal represents the need for full clarity regarding the expectations
about and the purpose of the knowledge product.
• Alignment area Tasks and Authority indicates that a project manager should define
the tasks and responsibilities within his/her research team and should also assure
a clear agreement on the rights and responsibilities of both the commissioning
organization and the research institute within the project to avoid debate at a later
stage.
• Alignment area Quality implies that the scientific models, concepts and definitions
used during the research can have a significant bearing on the findings and need
agreement already at the start. This is to avoid dismissal of an unfavorable research
result by arguing that the approach was flawed.
• Alignment area Consultative Structure focuses on the need to ensure both capacity
and time to allow for adequate interaction during the research process. There is
also attention for planning exchange of knowledge with intended users.
• Alignment area Vertical Alignment stresses the importance of vertical embedding
of the product within the organization for its legitimacy towards the commissioner
and the resources and capacity required. It is essential to refer any problems,
difficulties, or obstacles, which cannot be resolved at the research level to a
higher hierarchical level. Conversely, the higher hierarchical level should inform
researchers on specific issues that may influence there project.
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• Alignment area Organizational Environment is about identification of the
characteristics of the different involved organizations. The institutional work culture
of the commissioning organization may influence the process and the dynamics of
its context are important to understand the commissioner’s motive. Furthermore,
developments in the own organization should be well known and understood.
• Alignment area Relevance and Timing points out that the commissioner’s
requirements with regard to the purpose, form, and timing of the product may
change over time, even after approval of the original project proposal. Any changes
to the process itself may then be necessary. Furthermore, awareness about any
political sensitivity with respect to wordings and formulation of research results is
important.
• Alignment area Presentation reflects the need to agree timely on the form and
presentation of the knowledge products and their dissemination.
Part B: Development of the R4P Tool
Methods
We developed a reflection tool for researchers called R4P with the purpose to support
researchers in reflecting on their project to identify the need for alignment efforts during the
research process. Based on the findings in the first stage as described in the “Background”
section, we formulated the following specifications:
• The R4P tool should support users in engaging in systematic reflection on the
research process.
• The R4P tool should take into account the alignment areas identified in the case
studies.
• The R4P tool should be generally and easily usable at project team level.
In order to comply with the specifications, we decided to include open-ended questions
that would promote awareness and critical reflection on the process aspects of the project,
while taking into account the alignment pitfalls that we identified in the case studies by
contribution mapping. In this way, we intend to increase researchers’ sensitivity to the
context of their project and to the policy-making process. As they become more context-
sensitive, researchers will be more capable of recognizing and acting on the importance of
alignment with the commissioning and other organizations, in order to enhance the impact
of their work. At the same time, they will be more capable of acknowledging the different
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roles and responsibilities of researchers and policy-makers, and taking into account the
need to stay independent.
Step 1: Preparing the first part of the R4P tool
We first prepared the part of the R4P tool, which focuses on the Formulation Phase
of a project. In iterative, open sessions, our research team, consisting of the two acting
researchers and their supervisors (two senior researchers and two university professors),
discussed the formulation and categorization of the open-ended reflection questions and
the accompanying explanation for each question until consensus was reached. They were
concisely formulated and we added a brief explanation to each question to provide some
background concerning the question (Additional file 2: Draft R4P tool, part Formulation
Phase).
Step 2: Testing the R4P tool during the Formulation Phase
We asked three experienced project managers who work on policy-orientated research
projects in the field of public health and health care to test the Formulation Phase questions
of the R4P tool for usability in their projects during the upcoming new project cycle (2013/
2014). In August 2013, each project manager received a verbal explanation of the R4P tool.
They were asked to use the tool in the Formulation Phase of new projects for the year 2014.
After 3 months, they were interviewed face to face and asked to provide feedback on the
tool (Additional file 1: Topic list). Each semi-structured interview took approximately 1 h and
was recorded and analyzed by mapping.
Step 3: Developing an extension of the R4P tool for the Production Phase
For use in the Production Phase, we developed an extension of the R4P tool in a similar
process as the development of the Formulation Phase part. Based on the project managers’
feedback on the part for the Formulation Phase, we added examples to the Production
Phase questions. The examples illustrate the rationale of each question and concretize the
rather general wording of the questions (Additional file 2: Draft R4P tool, part Production
Phase).
Step 4: Testing the extension of the R4P tool during the Production Phase
Again, we asked the same three experienced project managers to use the R4P tool in the
production phase of their project during the year 2014. They were interviewed face to
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face and asked to provide feedback on the tool (see Additional file 1: Topic list). Each semi-
structured interview took approximately 1 h and was recorded and analyzed by mapping.
Step 5: Preparing the final version of the R4P tool for all phases
To complete the R4P tool, we integrated the Formulation Phase and Production Phase
questions and added examples from our case studies to the questions of the Formulation
Phase. Based on the project managers’ feedback, we decided to organize the questions
according to content rather than by project phase. We classified the questions into four
categories: organizational environment of the project (I), goal of the project (II), interaction
during the project (III), and outcome of the project (IV).
In the final version of the R4P tool, we provided an overview to indicate in which phase of
the research project each question could be relevant, and we included clickable links to the
questions. The questions themselves also contain clickable links to explanatory notes to the
questions, as well as corresponding examples (Appendix Chapter 6: Additional file 3: Final
R4P tool).
Results
Step 2: Testing the R4P tool during the Formulation Phase
In step 2, we tested the part for the Formulation Phase, which included ten questions in
five categories (Additional file 2: Draft R4P tool, part Formulation Phase). When providing
their feedback on this part of the draft R4P tool, the project managers regarded the topics
raised in the open-ended questions as the key topics to address during the research process.
However, they indicated that they experienced the questions as rather abstract, which made
it more difficult to link them to their daily practice. Therefore, we added examples to the
question for the Production Phase.
Step 4: Testing the extension to the R4P tool during the Production Phase
The project managers considered the examples provided in the Production Phase questions
to be very helpful in clarifying the questions and in finding an approach for alignment in
comparable situations. They pointed out that they experienced some overlap between
the Formulation Phase and Production Phase questions and stated that they regarded
the tool as already suitable for (anticipating on) the extension phase. They were in favor
of a single integrated R4P tool with questions for all phases. After all, they considered
the R4P tool a useful checklist for addressing the important process topics of a research
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project. They indicated that the R4P tool should be readily accessible not only to health-
systems researchers but also to researchers in other expertise domains and to RIVM are
commissioning clients, such as policy-makers working at the Ministry of Health, Welfare and
Sport. The project managers suggested using the R4P tool for education of project managers
as part of the regular project management courses. They also suggested making the tool
more user-friendly, for example, by making it available online and adding clickable links.
Step 5: Final version of the R4P tool for all phases
Based on the feedback of the project managers, we decided to merge the two parts of the
R4P tool into one list of questions for all phases. The final version of the R4P tool contains
23 reflection questions and is presented in an additional file (Additional file 3: Final R4P
tool). The list of questions contains clickable links to explanatory notes to the questions and
corresponding examples. The examples have been derived from our case studies and reflect
real-life situations recognizable for RIVM researchers. Most questions are relevant for both
the formulation phase (21 of 23) and the production phase (22 of 23), whereas ten questions
are relevant for the extension phase. To indicate in which phase of the research project each
question can be relevant, the first page provides an overview including clickable links to the
questions.
Discussion
The Contribution Mapping approach in our case studies provided us with useful insights
into important areas for alignment between researchers and policy-makers in the field of
public health and health care. We integrated the alignment areas into one list by a cross-
case analysis. In line with the work of de Goede and of Kok and Schuit, the anticipated
alignment areas “goal,” “quality,” “consultative structure,” “relevance and timing,” and
“presentation” focus on the optimal interaction between researchers and policy-makers [16,
17]. However, the identified additional areas “tasks and authority,” “vertical alignment,” and
“organizational environment” are more connected to the context of the research project.
We found that these context topics strongly influence optimal interaction and alignment
with policy-makers. Researchers were not always aware of the context in relation to their
project and of its influence on their own interaction and alignment with policy-makers.
Therefore, it is important for researchers to comprehend context issues in relation to their
project and to act upon them in aligning with policy-makers.
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We argue that the R4P tool can be useful for other public health and health systems research
projects, since it focuses on process issues that are relevant to most research projects.
The case studies enabled us to translate the alignment areas into reflection questions and
illustrative examples that can be used in daily practice. Furthermore, we identified several
important topics that relate to improving the contributions of scientific knowledge to policy-
making and that offer ways to facilitate alignment efforts and thus enhance contributions to
evidence-based policy-making. These findings can be of interest for researchers conducting
research in commission of governmental organizations.
All phases of the research process require alignment efforts
For an individual researcher, alignment with policy-makers is the most practical way to
influence the contributions of their research and knowledge [24]. Schut et al. also concluded
that researchers have to address the challenges of the complex dynamics of policy-oriented
research through reflection and context sensitivity [25]. Alignment requires awareness of
emerging issues and continuous efforts at various levels. Both the case studies and the
exploratory pilot project showed that personal interactions between individuals — both
in the organization conducting the research and in the commissioning organization — are
crucial for alignment. In our case studies, personal interactions between researchers and
policy-makers occurred mainly during the production phase of a research process, being
the lengthiest phase. However, we want to point out that informal interactions during
the formulation phase and the extension phase are equally important. In the formulation
phase, interaction can prevent an unarticulated knowledge question, a request for research
being so imprecisely formulated that it does not represent the exact knowledge need and
may have a negative impact on the outcome of the project beforehand. At the end of the
production phase, knowledge is mostly presented in a knowledge product, such as reports,
scientific papers, websites, or databases. In the extension phase, interaction may ensure
that the level of interest in the knowledge products does not decrease quickly.
We acknowledged that project managers have to align on topics relevant for the Extension
Phase already during the Formulation and Production Phase. Although the Three-Phase-
Model proved to be helpful in the analysis of the case studies, we departed from the
separation into three phases for the R4P tool. One list of reflection questions turned out to
be more convenient than a list for each separate phase due to the overlap in topics.
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Alignment has to be organized
To facilitate better alignment in all phases, knowledge institutes should pay explicit attention
to and recognize the everyday process issues associated with knowledge production. For
knowledge institutes, it can be very useful to analyze their organizational routines and
reserve budget for developing awareness of context issues and interactions with policy-
makers. Individual researchers will be encouraged to pay attention to the process issues
associated with research if they are rewarded for doing so, for example, when sufficient
time and appreciation is devoted not only to the scientific merits of their work [26]. For
commissioning organizations, it is just as important to take the need for organizing alignment
into account.
Vertical alignment is crucial
Our experiences in our research suggest that many researchers prefer to pay attention to
scientific issues rather than spending time to alignment. Thus, the urgency of devoting
attention to alignment must be made clear to researchers, since a single, well-aligned
knowledge product that really offers a contribution will often be preferable to a large
number of knowledge products that are of little practical use. However, this aim cannot
solely be achieved at research level, but requires efforts and collaboration at all hierarchical
levels of both organizations (i.e., the knowledge institute and the Ministry) during the
entire research process. It is crucial that all parties involved are aware of their role in the
research process and assume their responsibilities while taking into account those of the
other organization. Although alignment is essential to enhance contributions to policy-
making, knowledge institutes must simultaneously balance adequate alignment with policy-
makers with sufficient distance from the policy-making domain if they wish to maintain
their independence. Internal vertical alignment between researchers, project managers,
and line management of the knowledge institute is essential to optimize both alignment
and independence and to strike the right balance.
Usability of the R4P tool
During our project, we found that theoretical considerations on alignment and knowledge
contributions have little appeal to health systems researchers. Therefore, the understanding
of important alignment areas and the topics they represent had to be “translated” in order
to be useful to researchers in their everyday work. In the R4P tool, the combination of
reflection questions based on research findings and illustrative examples from the case
studies with situations familiar to the researchers particularly offered added value.
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Although our reflection tool is based on translation of alignment areas derived from case
studies in our own institute, we argue that the tool could also provide a basis for reflection
in other research projects, both for researchers and policy-makers, since the topics covered
are process-related and the tool can be used in a flexible way. The present tool includes 23
questions that cover all important alignment areas. It is up to users to decide whether they
are relevant to their particular project at a given point in time and whether the answers to
the questions have to result in an alignment effort.
Conclusions
Aligning to the needs of policy-makers offers researchers the opportunity to take influence
into their own hands in an ever-changing context, such as the policy priorities of the
Ministry, the influence of political reality on the relevance of their knowledge products, and
the organization of their own research institute. We found that reaching alignment is not
easy at all and depends on many aspects. In our study, we first identified the most important
aspects for researchers in government-commissioned research. By cross-analysis of the case
studies, we could identify eight key alignment areas: the goal, quality, relevance, timing,
and presentation of research (findings), the tasks and authorities of actors, the consultative
structure and vertical alignment within organizations, and the organizational environment.
The R4P tool is based on these areas. We intended to develop an instrument that supports
researchers in undertaking alignment efforts to enhance the contributions of their work
to policy-making. Researchers recognized the questions — which were illustrated with
examples from case studies— as relevant and to the point. The R4P tool can be deployed
in any health systems research project to reveal the topics that are most important in the
project. Initial experiences in using the R4P tool show that it offers useful alignment guidance
to researchers and facilitates reflection on process issues, which will help researchers to
adopt a more context-sensitive approach in their work. By regular reflection, researchers
will be better able to decide what to do or not.
Since the questions in the tool are intended for inspiring reflection, it is not necessary to
answer completely all questions at the same time. It is up to the users which topic they
want to reflect on depending on the phase and characteristics of a specific research project.
By thinking about the answer to the questions, researchers gain insight into the ongoing
process and become aware of what action is needed and how to anticipate on the policy-
making reality. The tool can be used as a checklist by individuals and as basis for open
discussion in project teams. The R4P tool may also provide a basis for dialogue between
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researchers and policy-makers, turning it into a shared tool for alignment. For the use of
the R4P tool as shared guidance in the dialogue between researchers and policy-makers,
the next step will be to assess its applicability for policy-makers and any need for adaption.
Finally, the ultimate step will be to investigate the influence of using the R4P tool on actual
knowledge contributions to policy-making.
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17. Kok MO, Schuit AJ. Contribution mapping: a method for mapping the contribution of research to enhance its impact. Health Res Policy Syst. 2012;10:21.
18. RIVM. National Institute for Public Health and the Environment. Available from: http://www.rivm.nl/en. Accessed 21 September 2015.
19. Kok MO, Gyapong JO, Wolffers I, Ofori-Adjei D, Ruitenberg J. Which health research gets used andwhy?Anempiricalanalysisof30cases.HealthResPolicySyst.2016;14(1):36.
20. Hegger I, Janssen S, Keijsers J, Schuit AJ, van Oers, HAM. Analyzing the contributions of a government-commissioned research project: a case study. Health Res Policy Syst. 2014;12(1):8.
21. Hegger I, Kok MO, Janssen SJ, Schuit AJ, van Oers HAM. Contributions of knowledge products to health policy: a case study on the Public Health Status and Forecasts Report 2010. Eur J Pub Health. 2016; 26(6):922-927.
22. Hegger I, Marks LK, Janssen SW, Schuit AJ, van Oers, HAM. Enhancing the contribution of research to health care policy-making: a case study of the Dutch Health Care Performance Report. J Health Serv Res Policy. 2016;21(1):29–35.
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23. Khan S, Van Wynsberghe R. Cultivating the under-mined: cross-case analysis as knowledge mobilization. Forum Qual Soc Res. 2008 9(1). Art. 34.
24. Gold M. Pathways to the use of health services research in policy. Health Serv Res. 2009;44(4):1111–36.
25. Schut M, van Paassen A, Leeuwis C, Klerkx L. Towards dynamic research configurations: a framework for reflection on the contribution of research to policy and innovation processes. Sci Public Policy. 2014;41:207–18.
26. Briggs SV. Integrating policy and science in natural resources: why so difficult? EcologicalManagement & Restoration. 2006;7(1):37–9.
27. Westert GP, van den Berg MJ, Zwakhals SLN, de Jong JD, Verkleij H. Dutch Healthcare Performance Report 2010. Bilthoven: RIVM; 2010.
28. Van der Lucht F, Polder JJ. Van gezond naar beter. Volksgezondheid Toekomst Verkenning 2010. Bilthoven: RIVM; 2010.
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Additional files
Additional file 1: Topic list.
Additional file 2: Draft R4P tool.
Additional file 3: Final R4P tool
available at DOI 10.1186/s13012-016-0496-1
Appendix Chapter 6
Additional file 3
Final R4P tool
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Research for PolicyResearch Project
FormulationPhase ProductionPhase Extension Phase
R4P TOOL R4Pquestions R4Pquestions R4Pquestions
Organizationalenvironmentoftheproject
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Goal of the project 070809
11
13
07
0910111213 13
Interactionduringtheproject 1415161718
1415161718
141516
18
Outcome of the project 1920212223
1920212223
1920
2223
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I: Organizational environment of the project
1.Whatorganizationswill be involved in theproject and inwhat capacity?What is the
position of these organizations within the health domain of the project, and what are the
practicalimplicationsofitsposition?Explanation and example 1
2. What are the (current) characteristics of the commissioning organization and its
relationshipwithyourorganization?Howdoyouaddressthesefactorsduringtheprocess?
Explanation and example 2
3. In what (dynamic) context does the commissioner operate during the project, and what
implicationscouldthishavefortheprojectitself?Explanation and example 3
4. In what dynamic context does your institute operate, and what implications could this
haveforyourprojectandthealignmentwiththecommissioner?Explanation and example 4
5. What are the specific characteristics of the researchers on your project team? How
are tasks and responsibilities dividedbetween them, andhow is thework coordinated?
Explanation and example 5
6. Are there any problems which prove impossible to be resolved at project level, whereby
higherorganizationallevelsmightbeofassistance?Explanation and example 6
II Goal of the project
7. How and when should the research product be used according to your organization and
thecommissioningorganization?Whatisitspurpose? Explanation and example 7
8. What is the underlying concern of the research question in relation to the problem that
thecommissionerwishestosolve?Explanation and example 8
9. To what extent is it possible to refine the research question at a later stage of the research
process to bring itmore closely in linewith the commissioner’s need?Explanation and
example 9
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10. Has the commissioning organization experienced any changes which may affect their
knowledge need since the project proposal was produced? Does the research question
formulatedintheprojectproposalcontinuetoaddressthecurrentknowledgeneed?Isit
necessary(andpossible)toamendtheprojectplan?Explanation and example 10
11.Withinwhattimeframedoesthecommissionerrequiretheproductandwhy?Didyou
agreeontheprojectschedule?Areallphases,milestonesanddeliverablesclearlydefined?
Explanation and example 11
12. Have the scientific models, concepts and definitions to be applied within the project
beenagreedbyallparties?Explanation and example 12
13. Did you explicitly agree on the rights and responsibilities of both the commissioner and
yourinstitutewithintheproject?Explanation and example 13
III Interaction during the project
14.Withwhomshouldyoualignwithinyourownorganizationduringtheprocess?Whose
commitmentmustbesoughtandhow?Explanation and example 14
15. With whom should you align externally during the process and whose commitment
mustbesought?Explanation and example 15
16. What type and frequency of consultation with the commissioner will be most appropriate
totheprocess? Explanation and example 16
17. Did you plan any interim knowledge exchange with the commissioner regarding the
contentoftheresearchproduct?Explanation and example 17
18. How do you achieve interim exchange of knowledge between the various users?
Explanation and example 18
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IV Outcome of the project
19. What types of user (at various levels within the commissioning organization) can be
identified for the intended product, and how is their diversity to be taken into account in
termsofcontentandprocess?Explanation and example 19
20. How do you monitor the production of (similar) knowledge products by other
organizations, and the influence that such products may have on the commissioner and end
usersduringtheproject?Explanation and example 20
21. Do you have a timely discussion with the commissioner with regard to the form of the
researchproduct? Explanation and example 21
22. Do you envisage to draft a plan for the presentation and dissemination of your research
product, and has this been agreed well in advance with both the commissioner and relevant
internalstaff? Explanation and example 22
23. Have the higher organizational levels within both your institute and the commissioning
organization been made aware of the (expected) research results and the product forms
wellinadvance?Explanation and example 23
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Explanation Questions
I: Organizational environment of the project
Question 1
Whatorganizationswillbeinvolvedintheprojectandinwhatcapacity?Whatistheposition
of these organizations within the health domain of the project, and what are the practical
implicationsofitsposition?
Explanation question 1
It is important to identify: What are the characteristics of the different organizations
in question? What is their position (in relation to your organization’s network, e.g.
commissioner, project partner, subcontractor). What authority or influence do they possess,
andhowcanthisbeexploitedintheinterestsoftheproject?
Example 1
The issue
An independent governmental organization is in charge of a database containing confidential
health care information and this data is only provided for supervision purposes to the Health
Care Inspectorate. Since your project is commissioned by the Health Care Inspectorate to
support them in their tasks, the Health Care Inspectorate puts a data set from the database
to your disposal. However, the independent governmental organization is not involved and
raises objections to the use for research purposes in a meeting with your manager later in
the process.
The outcome
To resolve the issue, your manager aligns with the organization and the Health Care
Inspectorate. They agree to inform each other in future.
Question 2
What are the (current) characteristics of the commissioning organization and its relationship
withyourorganization?Howdoyouaddressthesefactorsduringtheprocess?
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Explanation question 2
It is important to identify: What are the characteristics of the commissioning organization
(e.g. Health Care Inspectorate, Ministry of Health, or other ministry), including its
institutional work culture. Attention should also be devoted to the commissioner’s role
within the research process (e.g. as a member of a steering group or advisory committee)
and the degree of ‘formal’ involvement.
Example 2
The issue
Your commissioner, the Inspectorate, supervises health care practices in your country,
maintains the law and as a result, is often the target of media attention. This clarifies why
inspectors are expected to act both in an authoritative manner and in a very carefull way.
In your own research project, the inspector involved wants to have full control and insists in
being involved in decisions on methods and in publications. According to his workculture,
he persists on his position despite your referring to your institute’s independent position.
The outcome
Since this divergence of views cannot be solved at project level, you ask your manager to
align with the inspector’s manager. They agree on the existing operating procedure ensuring
both sufficient information for the Inspectorate and independence for the researchers.
The inspector involved is informed by his manager on the agreed operating procedure and
takes now another position in the project. In return, you commit to inform him on draft
publications in order to avoid surprises.
Question 3
In what (dynamic) context does the commissioner operate during the project, and what
implicationscouldthishavefortheprojectitself?
Explanation question 3
To monitor the context in which the commissioner is operating, is essential to understand
any unexpected course of action and to be able to discuss this with a view to understanding
the commissioner’s motives.
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Example 3
The issue
At the commencement of your research project, the commissioner’s contact person asks
you to be kept fully informed of the decisions and choices made by your research team.
Two months later, it turns out to be impossible to contact her in time, because she does
not answer the phone, responds to emails only after a lengthy delay and, according to her
secretary, has no time to schedule a meeting. Meanwhile, there have been media reports of
an urgent reorganization within the commissioning organization, prompted by the minister’s
desire to show effective leadership following a number of incidents. This clarifies why the
contact person is preoccupied with other matters.
The outcome
You align with the head of department to decide how best to proceed. You agree to delegate
the issue to the account manager. She contacts the commissioning organization and via this
route, your contact is restored.
Question 4
In what dynamic context does your institute operate, and what implications could this have
foryourprojectandthealignmentwiththecommissioner?
Explanation question 4
External parties generally regard your research institute as a single, integrated organization.
It is however important to devote attention to the activities and developments at the
various levels within your institute and its individual departments in order to ensure
uniformity, avoid overlap and address circumstances which may affect your institute as a
whole. Matters to be considered include strategic plans, alignment between your institute
and commissioning organizations at management level, new tasks and responsibilities for
your organization, and other research projects or reports.
Example 4
The issue
Your institute publishes a report about the adverse effects of cycling in traffic, notably
the inhalation of fine particulate matter from exhaust fumes. A week later, your institute
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publishes another report in which it advises local authorities to encourage people to cycle
to work as a form of healthy exercise.
The outcome
The institute has unintentionally issued conflicting messages, causing confusion and
attracting adverse media attention. The director of the institute is asked to explain this to
both the Ministry of Health and the Ministry of Environmental protection. He commits to
improve the institute’s internal communication.
Question 5
Whatarethespecificcharacteristicsoftheresearchersonyourprojectteam?Aretasksand
responsibilitiesexplicitlyattributedtotheteammembers?Howistheworkcoordinated?
Explanation question 5
It is important to consider whether all necessary competences and expertise are represented
within the team. The tasks should be clearly designated, for example to specialists in
communications, media, design, data collection, etc. All team members should be aware of
the purpose and deadlines of the product.
Example 5
The issue
In a major project, the project managers involve all relevant experts with respect to the
complicated public health issues that will be investigated during the project. They carefully
keep guard over the scientific quality of their reports and they present their findings at
many acedemic occassions. Surprisingly, the commissioner expresses some dissatisfaction
about the outcome. It turns out that this is caused by the many delays in the process and
the unwelcome media message that came out of the public presentation of the final report.
The outcome
Apperently, necessary project management competences were not available at an adequate
level. To avoid this type of difficulties in future, it was decided that to add a researcher with
extensive process management competences to the project team and to put her in charge
of managing the process.
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Question 6
Are there any problems which prove impossible to be resolved at project level, whereby
higherorganizationallevelsmightbeofassistance?
Explanation question 6
If there are any problems, difficulties or obstacles which cannot be resolved by the project
coordinator and/or the commissioner’s contact person, it is essential to refer the matter to
a higher hierarchical level.
Example 6
The issue
In a project, the researchers are not provided with the data which has been promised by the
commissioner, although the data is crucial to the project. The commissioner’s contact person
says that he is unable to help since the data turn out to be confidential. The researchers
cannot proceed.
The outcome
The project coordinator aligns with the head of department to discuss ways in which this
problem can be resolved. In his turn, the head of department contacts the director, who
discusses the issue with both his counterpart at the commissioning organization and they
agree on the conditions for using the confidential data. After taking some measures, the
researchers receive the data and continue with the project.
II Goal of the project
Question 7
How and when should the research product be used according to your organization and the
commissioningorganization?Whatisitspurpose?
Explanation question 7
You need full clarity regarding the expectations which the product is to meet. In the case of
a research report for the Ministry of Health, for example, the parties should agree the point
within the policy process at which it is to be used, and the nature of that use.
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Example 7
The issue
Your two-yearly reports are intended to provide input at different moments in the policy
cycle. It is a major job to collect all data and to integrate them in a report every two years.
However, policy-makers indicate that policy realities constantly change and that they need
more up-to-date data.
The outcome
After a constructive discussion, you agree to start a website to present all data. This website
will be updated four times a year.
Question8
What is the underlying concern of the research question in relation to the problem that the
commissionerwishestosolve?
Explanation question 8
You need clarity with regard to whether the research question and its interpretation
adequately address the commissioner’s need. Conversely, and depending on the type
of product and the anticipated results, it may also be necessary to examine whether the
commissioner will be able to implement an adequate response based on the research
findings and whether adequate policy instruments are available to do so. You have to be
aware that the commissioner can be confronted with queries or criticism on the research
from the professional field, parliament, the media, etc.
Example 8
The issue
The Ministry of Health submits a research question to investigate prevention of obesity in
children. The question is rather vaguely articulated and for the researchers, it is not clear what
exactly made the commissioner submit the question. Is there need for information on the
trends in the number of obese children, on their geographical distribution, on effectiveness
ofinterventions,oneffectivenessofpubliccampaigns,ontheroleofyouthhealthcare?All
these issues have been addressed already. In a discussion with policy-makers, they indicate
that obesity in children will become a key issue in a new national prevention plan starting
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soon. The research should explore (policy) options to enhance healthy food uptake and
physical exercise at a local level. The results are awaited within half a year.
The outcome
It is agreed to discuss any findings after three months to align on recommendations. The
results will be presented in an infographic that can be used by local policy-makers.
Question 9
To what extent is it possible to refine the research question at a later stage of the research
processtobringitmorecloselyinlinewiththecommissioner’sneed?
Explanation question 9
A ‘broad’ research question is not necessarily a bad thing since you will have greater
discretion to define your own focus, which will emphasize the organization’s independent
scientific position. You don’t have to specify all research requirements in advance if you
create opportunities for further refinement and coordination during the research process
(e.g. by means of scheduled consultation meetings).
Example 9a
The issue
The Ministry of Health requests a Public Health Status and Forecasts report for which the
research question is very generally formulated. It is agreed that defining the themes is an
integral part of the project.
The outcome
In the first period of the production phase, the researchers can take certain time to reflect
on the themes and to align with policy-makers and scientists in planned meetings. They
finish the report in time.
Example 9b
The issue
The Inspectorate asks for a model to select inspection objects. At the start of the project,
the researchers need a lot of time to find out what the inspectors exactly expect and need.
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This extension of the formulation phase was not foreseen in the project plan and causes
delay already at the start of the project. At a later stage, lack of both time and budget hinder
the project.
The outcome
For future projects, the project manager firmly resolves to plan time and budget for further
definition of the project in the production phase to avoid problems at the final stage.
Question 10
Has the commissioning organization experienced any changes which may affect their
knowledge need since the project proposal was produced? Does the research question
formulatedintheprojectproposalcontinuetoaddressthecurrentknowledgeneed?Isit
necessary(andpossible)toamendtheprojectplan?
Explanation question 10
The commissioner’s requirements with regard to the purpose or form of the end product
may change over time, even after approval of the original project proposal. It is important to
ascertain whether this is the case on a regular basis, and to consider whether any changes
to the process itself are then necessary (and possible).
Example 10
The issue
A commissioner wishes to commission research examining the risks of a new technology
used in hospitals, as a follow-up to an earlier study. You formulate a proposal but before the
project itself starts, a serious incident involving a different type of technology takes place.
This causes significant media attention and the commissioner is subject to severe criticism.
It is now far more important for the commissioner to gain further knowledge about this new
technology than about that covered by your original proposal.
The outcome
In consultation with you, a new focus and a different approach are adopted.
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Question 11
Withinwhattimeframedoesthecommissionerrequiretheproductandwhy?Didyouagree
ontheprojectschedule?Areallphases,milestonesanddeliverablesclearlydefined?
Explanation question 11
The exact moment of the product’s finalization and/or presentation can be important in
terms of its relevance and use.
Example 11
The issue
The commissioning Ministry requires an extensive research report to support an important
policy document which is subject to a very strict deadline. Given the deadline, not all
required research can be performed within time, but finalization after the deadline will
make the product far less relevant to the commissioner.
The outcome
The project team agrees on the minimum part of the product to be delivered before the
deadline.
Question 12
Have the scientific models, concepts and definitions to be applied within the project been
agreedbyallparties?
Explanation question 12
The scientific models, concepts and definitions used during the research can have a significant
bearing on the findings. It is possible to dismiss an unfavourable research result by arguing
that the approach was flawed. To ensure the acceptance and relevance of the product, it
is prudent to create support for the scientific basis among all stakeholders, including the
commissioning organization. It is also important to identify any (political) sensitivities about
the models or definitions.
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Example 12
The issue
In your project, you have to calculate the cost of a certain type of medical care. You find
that this type of medical care has various definitions in practice, with different interventions
and equipment being grouped under the same general heading. For the purposes of your
research, you opt to apply the definition followed by the majority of health care professionals
and for which reliable data sources are available.
The outcome
When the draft report is completed, the high cost calculation takes the commissioner
unpleasantly by surprise. The commissioner argues that your organization did not apply
the correct definition. It takes a long discussion to convince the policy-makers of the
correct method. To compensate for the commissioner’s objection, you decide to extend the
discussion on the definition used in your report.
Question 13
Did you explicitly agree on the rights and responsibilities of both the commissioner and your
institutewithintheproject?
Explanation question 13
General rules establish the rights and responsibilities of the parties involved in a project of
your institute. However, it is also important to examine whether any specific agreements are
required with regard to aspects such as the ownership of data, the procedures for providing
feedback on draft versions of the product, and intellectual property rights.
Example13
The issue
A commissioning organization wishes to have three of its staff review a draft report.
However, one of the three is extremely slow to do so. Clear agreements have been made
with regard to the review process and the action to be taken further to the reviewers’
comments (Your institute retains full editorial control and will decide whether to make any
suggested changes). In addition a time limit has been set, i.e. the annotated version must be
returned within two working weeks.
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The outcome
The research coordinator decides to present the commissioner’s contact person with two
options: either the completion deadline remains unaltered and the third reviewer’s input
is disregarded altogether, or the deadline will be deferred to allow time for this reviewer’s
comments to be taken into consideration. The new agreement is recorded in writing.
III Interaction during the project
Question 14
Withwhom should you align within your own organization during the process?Whose
commitmentmustbesoughtandhow?
Explanation question 14
Vertical imbedding of the product within your organization is important for its legitimacy
towards the commissioner, the resources and capacity required (determined in part by the
desired quality and form of the product) and own future use or further research.
Example 14
The issue
During the production phase of a major project, the project team informs the director on
the proceedings in regular meetings. In the final stage of a theme report, a director at the
Ministry of Health is dissatisfied with its publication form, a flyer instead of a formal report
and he immediately contacts the director of the research institute.
The outcome
Being well informed, the director of the research institute is able to respond adequately on
the complaint. The directors agree on a compromise, a formalized brochure and additional
budget to complete a research report.
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Question 15
With whom should you align externally during the process and whose commitment must
besought?
Explanation question 15
In advance of the research process, you should identify the persons with whom alignment
is required (also with a view to the intended recipient of the product). You should also
determine how contact can best be established and maintained.
Example 15
The issue
Your institute is asked to conduct a major research project on public health. Two other
research institutes are very disappointed that they were not charged with this project.
The outcome
Since you need their expertise and wish to maintain a good relationship, you decide to
invite them for a stakeholder meeting before the project starts. You agree to include several
experts from both institutes in the project team and to organize a management meeting
twice a year. All organizations are satisfied with this outcome.
Question 16
What type and frequency of consultation with the commissioner will be most appropriate
totheprocess?
Explanation question 16
You should ensure that both capacity and the time schedule allow for adequate interaction
and consultation. Agree the form that such consultation will take (e.g. face-to-face, via social
media, email etc.) with all parties concerned.
Example 16
The issue
The contact persons of the commissioning organization are very busy people and it is difficult
to contact them. At the start of the project, you agree on different communication forms.
Four meetings are planned for the whole year. Furthermore, you start an online community
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to discuss upcoming issues in the meantime. Any interim questions will be solved by e-mail
or by phone.
The outcome
After several months, it turns out that the online community is hardly used. However, the
planned meetings prove to be very important for alignment with the commissioner. In the
next meeting with the commissioner, you agree to plan an extra meeting and to change the
function of the online community into a repository of background information.
Question 17
Did you plan any interim knowledge exchange with the commissioner regarding the content
oftheresearchproduct?
Explanation question 17
The intended effect of the research product can be increased or achieved somewhat sooner
by scheduling discussions of the interim results (before completion of the project and its
final report). It is important to discuss possible research outcomes with the commissioner
at the earliest possible opportunity, in order to allow all parties to be adequately prepared
for the implications of a particular finding.
Example 17
The issue
You foresee that your research results will not be politically expedient for the Ministry of
Health. In an early stage, you share the results with your contact person and with your
manager.
The outcome
Although the Ministry is not in the positin to influence your research results, timely
discussion with policy-makers give them the opportunity to prepare an adequate response
before your report is published. It must be remembered that such discussion relates solely
to alignment and anticipation. It does not entail the commissioner’s ‘approval’ of the results.
Your institute maintains its scientific independence and integrity by ensuring appropriate
internal alignment between all hierarchical levels of the organization.
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Question18
Howdoyouachieveinterimexchangeofknowledgebetweenthevarioususers?
Explanation question 18
The impact of the research product will be enhanced when there is interim discussion and
an exchange of knowledge between the various end users during the course of the project.
It is therefore useful for the project coordinator to know who alignst with those end users
on behalf of the commissioner, and what activities he or she undertakes in order to do so.
If the commisioner’s alignment efforts are not enough to ensure knowledge exchange with
the end users, it may be necessary for the project team to take action, involving the account
manager and his/her staff.
Example 18
The issue
A project has a steering group on which various directorates of the Ministry of Health are
represented. The project group collates and processes the steering group’s comments on the
draft versions of the final research report. Some directorates offer considerable feedback,
others little or none at all.
The outcome
After publication of your report, the project evaluation reveals that the directorates which
have provided least feedback also show least awareness of the report’s findings, yet are
the most critical with regard to its practical value. A steering group member who shows
considerable involvement and engagement in the process tends to engender greater
satisfaction. The project team decides that any follow-up project will involve closer alignment
with the commissioner’s contact person in order to determine the exact membership of the
steering group and the degree of involvement its members are expected to show.
IV Outcome of the project
Question 19
What types of user (at various levels within the commissioning organization) can be
identified for the intended product, and how is their diversity to be taken into account in
termsofcontentandprocess?
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Explanation question 19
There may well be several types of user within the commissioning organization (e.g. different
policy directorates, departments or hierarchical levels). Their diverse interests may demand
differentiation in terms of the presentation of the product, both in form and timing.
Example 19
The issue
For your project, you regard the policy-makers of the Ministry of Health as the intended users
of the knowledge products resulting from your project. All directorates are represented in
the advisory board of the project and you expect that your knowledge products will be
widely supported within the Ministry.
The outcome
In practice, it turns out that behind the scenes, your first report is not supported unanimously
within the Ministry and some policy-makers question whether your research should be
continued. You find that this mismatch can be attributed to the characteristics of the policy
directorates: one directorate acts more on general or system level whereas another is more
specialized in a specific health domain. This causes some directorates to feel less committed
than others, although during the advisory board meetings, the representatives do not
clearly express their discontent. You decide to spend frequently a workday at the Ministry
to enable informal meetings with representatives of the different directorates and to gather
information on their specific needs.
Question 20
How do you monitor the production of (similar) knowledge products by other organizations,
and the influence that such products may have on the commissioner and end users during
theproject?
Explanation question 20
Throughout the production phase, it will be useful to ascertain whether other research
organizations are working on similar or related products. It is also important to determine
the likely value of such products to the commissioner, and whether they will affect the
(perceived) relevance of your product. This will enable you to take these influences into
account in your project and in the alignment with the commissioner.
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Example 20
The issue
Another research organization intends to present a report at a large event just days before
you are due to publish a product relating to similar subject matter. This will inevitably distract
attention from your product. Moreover, inside information suggests that the conclusions of
the other report directly contradict your own findings. This could place the commissioner in
a particularly difficult situation.
The outcome
You decide to contact both the commissioner and the higher hierarchical levels within your
institute to align on the potential problems and the action required.
Question 21
Do you have a timely discussion with the commissioner with regard to the form of the
researchproduct?
Explanation question 21
Much research culminates in the publication of a report. However, it is possible that a different
form of product will be more useful to the commissioner. Examples of alternative products
include a summary of a scientific publication to support a policy decision, a presentation, or
an instrument such as a simulation model or a survey questionnaire. Knowledge presented
during a round-table discussion is also a ‘product’.
Example 21
The issue
A commissioner faces a particularly complex policy issue and requests your institute to
provide input for its internal deliberations. Out of habit, your commissioner asks for an official
report on the subject. However, you realize that a report will not meet the commissioner’s
knowledge need for their own exploration of the problem and cannot be delivered on time.
The outcome
Following consultation with the commissioner, it is agreed to prepare and host a
brainstorming session for the policy-makers concerned. Based on literature study, your
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team will also produce a background document and a presentation. On the outcomes of the
brainstorming session, the commissioner is able to base further action and decisions, and
to formulate terms of reference for a research project on the same topic to be conducted
the following year.
Question 22
Do you envisage to draft a plan for the presentation and dissemination of your research
product, and has this been agreed well in advance with both the commissioner and relevant
internalstaff?
Explanation question 22
Working to a set plan for the presentation and dissemination of the research product will
increase its outreach and hence the likelihood that the findings are acted upon in practice.
It is useful to plan the relevant activities during the course of the project itself, since there
may be neither time nor capacity once the product has been completed
Example 22
The issue
Despite some delays in a project, the deadline can still be met if staff works overtime. The
research product is completed just before the Christmas holiday, much to the relief of the
project team. When work resumes in January, the team is disbanded and its members
assigned to new projects. They have no time left for extended presentation or dissemination
of the former project’s results since these activities had not been planned and no budget is
available.
The outcome
During the new commissioning cycle by the Ministry, the researchers realize that their
previous research efforts did little to raise awareness of their findings. The policy-makers
show scant interest in the research findings and the Ministry commissions only limited
further research. The researchers discuss this disappointing result in their team and agree
to plan more time and capacity for dissemination in a new project they are working on.
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Question 23
Have the higher organizational levels within both your institute and the commissioning
organization been made aware of the (expected) research results and the product forms
wellinadvance?
Explanation question 23
The higher organizational levels can enhance the effectiveness and assimilation of a
product within the commissioning organization by drawing their counterpart’s attention to
the forthcoming product at the earliest possible opportunity. Moreover, the discussion of
relevant RIVM results at the senior management level supports the profiling of RIVM. It is
important that the higher organizational levels on both sides are aware of the forthcoming
results and conclusions so that no one is taken by surprise. The proactive transfer of
information about RIVM research results to the higher management levels is therefore
extremely worthwhile.
Example 23
The issue
Your institute is preparing a research report which has been commissioned by a specific
policy directorate within the Ministry of Health Your director reports on progress and the
expected results at a meeting of the Ministry’s Executive Council, whereupon a director at
the Ministry realizes that the report may well be relevant to his directorate and the Minister,
which he then informs accordingly.
The outcome
The publication of the final report prompts an unexpected discussion between various
field parties, a debate which inevitably attracts media attention. However, because your
director already informed the Minister of Health about the publication and the contents
of the report, the latter is able to field press questions when arriving at her next public
engagement.
Chapter 7
Discussion and Conclusion
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Introduction
This chapter starts with a short description of the study context, design and findings.
Following this short overview, we present a reflection on the findings in relation to the
research questions. Next, we reflect on the methodology used in this study. Finally, we
provide some perspectives for further research and we end with the conclusions of this
study.
Short description of the study context, design and findings
Context
National Public Health Institutes (NPHIs) have the task to support governments in
safeguarding public and environmental health by monitoring the health status of the
inhabitants, by conducting research and providing advice based on scientific knowledge. It
is part of the NPHIs’ job to contribute with scientific knowledge to policy and practice, which
appears to be difficult.
The National Institute for Public Health and the Environment (RIVM) in the Netherlands
describes its mission as follows on its website [1]:
‘How can we keep ourselves and our environment healthy? That is the challenge facing
government authorities at all levels, from the local to the international. The Dutch National
Institute for Public Health and the Environment (RIVM) carries out independent research and
provides policy advice to assist them in this task.’ Furthermore, the website also mentions
that RIVM places its knowledge ‘at the disposal of policy-makers, researchers, regulatory
authorities and the general public’.
Behind this concise description of RIVM on the website, a complex reality hides in which
researchers often experience that just producing and offering knowledge appears to be
insufficient for contributing to policy and practice. The complexity of a research institute’s
task to provide policy-makers effectively with scientific knowledge is well-recognized [2-4].
Research findings often find their way with difficulty to practice, which is certainly true for
policy-making. How to enhance knowledge utilization is a major issue in public health and
covers an extended research field nowadays [5-7]. This study aims to gain more insights in
ways for enhancing the contributions of government commissioned research in the NPHI
context.
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For our study on improving knowledge utilization, we defined two main research questions
(Chapter 1):
1. What alignment areas are important for enhancing the contributions to health
policy of government commissioned research conducted by National Public
Health Institutes?
2. Based on the empirical findings gained in this study, what is a practical approach
to enhance knowledge contributions from NPHIs to evidence-informed health
policy-making at national level?
Theoretical framework
Since we intended to find empirical insights at the level of the research project in our study,
we used the method Contribution Mapping developed by Kok and Schuit proceeding from
a constructivist perspective [8] (Chapter 1 and 2). According to Contribution Mapping,
knowledge has only impact if people put a meaning to it, which they will be more inclined
to do if knowledge is aligned with their own views, beliefs, ideas and concerns. Contribution
Mapping considers alignment between researchers and knowledge users important and
provides a method to investigate alignment efforts in relation to knowledge contributions,
which may show into options for improving knowledge utilization.
Study design
We gathered data by a qualitative case study approach [9]. We conducted three case
studies and analyzed these in line with the method Contribution Mapping. After this stage,
we conducted a cross-case analysis to identify areas where specific attention for alignment
is needed in a research project. Based on these alignment efforts and the findings from
the case studies, we developed a reflection tool for researchers at an NPHI [10]. Figure 7.1
provides a schematic representation of the study.
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Discussion and conclusion | 155
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Findings
Three case studies
In the first stage of our research (2011–2013), we conducted three empirical, qualitative
case studies (Chapter 3, 4 and 5) [11-13]. We gathered data by document analysis and by
semi-structured interviews with researchers, policy-makers and managers involved in the
projects. By coding and analysis, we identified alignment areas that were important for the
contributions of the project.
Three multi-annual RIVM projects from the Public Health and Health Care domain with
different characteristics and all completed in 2010 were selected as cases: “Development
of a Risk Model” (chapter 3); “Development of the Dutch Health Care Performance Report
2010” (chapter 4); and “Development of the Dutch Public Health Status and Forecasts
Report 2010” (chapter 5). These three cases had different characteristics, with the most
prominent differences their size and the increasing formal status of the knowledge products
in policy-making.
In the first case study “Development of a Risk Model”, the development of a risk-based
approach for clinical trial inspections in the Netherlands is described (Chapter 3) [11]. The
knowledge product was a risk model acting as an initial impetus for risk-based selection of
inspection objects. This knowledge product had to be further developed to become part of
the formal inspection policy at a later stage. It therefore retained a confidential, unpublished
status. We found that researchers and commissioning inspectors had divergent views on
their collaboration and the ownership of the knowledge product, but were not aware of
these different perceptions. Areas relevant for alignment in the project concerned not only
the project level, but also the organizational environment of the project and the formal and
historical relationship between the organizations. Although the project was distant from
the strategical level of both organizations and although both researchers and inspectors
involved were not (fully) aware of the historical relationship between the organizations, the
organizational environment and history proved important also at project level.
The second case study described the development of the Dutch Health Care Performance
Report 2010 (DHCPR) (Chapter 4) [12]. The DHCPR monitors the health care performance in
the Netherlands by using indicators for quality, accessibility, and affordability in commission
of the Ministry of Health, Welfare and Sport and aims to contribute to strategic policy-
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Discussion and conclusion | 157
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making. In this study, influence of the environmental complexity on alignment emerged.
Important alignment areas were familiarity with the commissioning organization and the
need for alignment with different ministerial directorates, but also with other knowledge
institutes. Furthermore, launching new product types, such as an infographic, also requires
specific alignment, such as on the purpose of the new product and its consistency with other
knowledge products. In this project, we observed that after retirement of a highly valued
double-role-actor, both policy-makers and researchers considered the lack of a successor as
a noticeable loss in the alignment repertoire for the DHCPR.
The third case study concerned the Dutch Public Health Status and Forecasts Report 2010
(PHSF 2010) (Chapter 5) [13]. The PHSF report is embedded in the national health policy
cycle by law and provides the policy themes for the National Health Memorandum. Its
contribution to health–policy making is thus formalized and direct. The PHSF2010 process
included established alignment efforts between researchers and policy-makers based
on about 20 years of experience with alignment from previous PHSF editions. However,
researchers still felt that more contributions could come out of this major project. We
identified areas for specific alignment that could help in enhancing contributions of the
PHSF: creating more awareness of the divergent, continuously changing actor scenarios
of stakeholders and more specifically of policy-makers at different places and levels in the
Ministry; working on vertical alignment within the organizations involved; and careful timing
of draft products to create early adopters.
Cross-case study
To find the most important alignment efforts, we conducted a cross-case study and analyzed
the findings of the three cases in conjunction (Chapter 6) [10]. We identified eight areas
for which alignment efforts are particularly relevant, which are summarized in Table 7.1.
The issues reflect which problems can be avoided by alignment, the topics indicate where
alignment efforts could focus on, for example by discussing them in joint meetings of
researchers and commissioners (Table 7.1).
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Table 7.1 Eight areas for alignment
Area for alignment Issue Topics to address
Goal Need for full clarity regarding theexpectationsaboutandthe purpose of the knowledge product
Theformulationoftheknowledgequestion;explorationofitsorigin,the‘questionbehindthequestion’andtheunderlyingneedforthe knowledge products
Tasks and authority Needtodefinetasksandresponsibilitieswithintheresearch team and to have clear agreement on the rights andresponsibilitiesofinvolvedorganizations
The input of all involved actors (both researchers and policy-makers); their responsibilities,knowledgeanddataexchange by actors during the process and thefinalauthorityovertheknowledgeproducts
Quality Needtosharethescientificmodels, concepts and definitionsusedduringtheresearch to avoid dismissal of an unfavorable research result
The research method; conceptual framework, and data used in the research project
Consultativestructure
Need to ensure both capacity andtimetoallowforadequateinteractionduringtheresearchprocess
Theconsultativestructureoftheproject;thesharingofrelevantinformationandtherelationshipsbetweenactors;double-roleactors
Verticalalignment Needforverticalembeddingof project and knowledge productwithinorganizationstoassuresufficientlegitimacyand resources
Interactionwithintheorganizationconductingresearchandwithinthecommissioningorganization;interactionbetween hierarchical levels and the embedding of the project in the organizations
Organizationalenvironment
Need to be familiar with thecharacteristicsofinvolvedorganizations,suchasinstitutionalworkculture, dynamics of the commissioner’s context and developments in the own organization.
The environment of the research project; awarenessofrelevantconditionsexternaltotheresearchprojectinfluencingtherelationshipbetweeninvestigatorsandlinked actors; incidents, media events, relationshipswithotherorganizations,changingprioritiesandchangingactors
Relevance and timing
Needtobecontextsensitiveand to be aware of any changes in the commissioner’s needs and requirements with regard to the purpose, form, andtimingoftheproduct.
Theformulationandwordingoftheresearchresultsandtimingofthedeliveryandpresentationoftheknowledgeproducts
Presentation Needtoagreetimelyontheformandpresentationoftheknowledge products and their dissemination.
The design and structure of knowledge products and the tools for the extension strategy
From: Hegger et al;Implementation Science. 2016;11(133) [10]
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Discussion and conclusion | 159
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Development of the reflection tool Research for Policy (R4P)
In the next phase of our study, we formulated a practical approach to translate our findings
for researchers working in government commissioned projects (Chapter 6).
Based on the eight alignment areas identified, we developed a reflection tool for researchers.
In this tool, we translated the important alignment areas into open concise questions to
support researchers in their reflection on the research process. In a pilot study, we asked
three project managers to test the two drafts of the R4P tool in their ongoing projects. They
indicated that the topics raised were in fact the key topics they experienced in their research
projects. They suggested making the tool more user-friendly, for example by adding clickable
links, and considered the examples from the case studies to illustrate the questions very
helpful. Taking account for their feedback, we finalized the Research for Policy tool.
The final R4P tool has a clickable format and all questions are illustrated with an example
based on the case studies (Annex 1). When using the tool for reflection, researchers can
decide themselves which questions they consider relevant at a certain moment. They can
also use it as a checklist to prevent overlooking important issues.
Reflection on the findings
In scientific literature, it is well recognized that knowledge push without adequate
alignment is usually insufficient to realize contributions [14-17]. For example, interaction
between researchers and policy-makers is widely considered an important precondition for
knowledge utilization in policy-making [15]. As we described in the introduction, this can be
understood by considering the different logic of policy-making in comparison to research
and science. Alignment efforts and moving towards each other are necessary to find the the
right balance between science and policy-making. In the case studies, we observed that this
common understanding was put into practice by formal and more informal alignment efforts
for coming to agreement with the commissioners. In the interviews, everyone stressed the
importance of meetings, knowing each other and understanding each other’s interests and
needs.
Nevertheless, another common feeling was that there is room for improvement, raising the
question ‘which buttons should be pushed to achieve this’. We initiated the current study
to find practical ways for improving knowledge contributions to health policy in addition to
already implemented approaches.
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The findings of the three case studies and the cross-case analysis provided us an answer to
the first research question:
What alignment areas are important for enhancing the contributions to health policy of
government commissioned research conducted by National Public Health Institutes?
From the case studies, we identified eight alignment areas that need specific attention to
prevent unaligned situations during the research project (chapter 6). The areas showed to
be consistent with many critical factors for knowledge utilization mentioned in scientific
literature [4, 14, 15, 18-23]. In addition, we consider the difficulty of reaching alignment in
practice also a crucial finding. As the saying goes, the devil is in the detail. We observed that
effective alignment is about ongoing attention to details, which makes reaching alignment
more complicated than often envisaged. Apart from procedures – such as organizing a
meeting-, effective alignment asks for awareness of the critical factors, for knowledge about
the other stakeholders’ concerns and for political sensitivity. For example, it is common
practice to consult the commissioner at the start of a project. However, if researchers are
insufficiently aware of the fact that behind the initial research question often other, actual
questions hide or that the commissioning organization may quite differently perceive the
concern or problem behind the research topic, they could unjustly assume that alignment
on the research question exists after a meeting. Wordings or professional jargon can have
a different meaning for researchers and policy-makers, causing different interpretations of
agreed objectives and terms.
Furthermore, the difficulty of reaching alignment is also caused by some burdensome
features of alignment efforts: they often ask much more time than anticipated and require
full attention. In the case studies and the pilot study for the R4P tool, some researchers
indicated that although they acknowledge the importance of alignment and undertaking
alignment efforts, they consider the scientific issues the main priority of the project and
the process issues as an additional task needing precious research time. We noticed that
researchers look at the process as the vehicle for bringing knowledge to the commissioner;
it should smoothly function and preferably cause no difficulties, extra costs or additional
time.
The case studies demonstrated the need for continuous awareness for non-aligned
situations teaching us that lack of alignment is often unexpected or even unnoticed. The
entire process needs alignment efforts, but what type of alignment effort is needed at what
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Discussion and conclusion | 161
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point in time can hardly be predefined. Researchers need more than little enthusiasm for
process issues in order to sustain in conducting alignment efforts apart from the agreed
consultation structure during the entire project.
These findings bring us to the second research question:
Based on the empirical findings gained in this study, what is a practical approach to enhance
knowledge contributions from NPHIs to evidence-informed health policy-making at national
level?
From the case studies, we learned that developing a set of generally applicable alignment
actions would not be the best solution for a practical approach to reach effective alignment.
Instead of operating rules, effective alignment needs continuous reflection on the process.
Researchers working on projects for contributing to health policy have to be aware of
the context of their research, while remaining independent at the same time [18]. Schut
et al affirm the importance of reflection among researchers and the promotion of more
embedded, context-sensitive and flexible research strategies [24].
These considerations made us decide to develop a reflection tool for researchers. Such a
tool would make our findings available in a practical way and can be applied in research
projects, regardless their characteristics such as subject, commissioner, phase, context,
seize, resources and political sensitivity (Annex 1). It is up to the researchers (and other
users) to determine the type and intensity of the alignment efforts needed.
However, this reflection tool can only be effective in an organizational framework that
meets some preconditions. As mentioned before, attention for process issues is difficult to
sustain and researchers need support by facilitating reflection and alignment efforts. The
most important preconditions are (1) a facilitating organization, (2) alignment as a two-
way process and (3) balance between scientific independency and alignment with the
commissioner’s needs. As we will explain, these preconditions also interrelate making the
challenge of enhancing knowledge contributions even more complex.
Facilitating organization
In their interaction, policy-makers and researchers have to take into account and have to deal
with the complex context, in which they operate. Strydom et al pointed out the influence
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of organizational factors on the uptake of evidence by policy-makers in the decision-
making process [18]. Our case studies have shown that the professional environment of
the NPHI also influences the level at which researchers (are able to) undertake alignment
efforts to enhance knowledge uptake by their commissioning counterpart [18]. Because
of their position at the nexus of science and policy-making, knowledge institutes such as
NPHIs are accountable to both the government and the scientific community and the first
organizational challenge manifests itself. This also implies that they have to meet both the
need for producing aligned commissioned knowledge products to serve the commissioning
organization and the need for publishing in scientific journals as rewarded by the scientific
community. As we mentioned before, we observed that the researchers’ focus was often
primarily on the scientific issues and the content of the knowledge products, whereas
the process issues and alignment efforts, although considered quite important, were
secondary. For researchers, a publication in a peer-reviewed scientific journal is a valuable
reward contributing to their scientific status. A reward for the backstage process tasks is
often less pronounced since many aspects are rather invisible and not quantifiable. NPHIs
should therefore consider whether they reward backstage alignment in sufficient balance
compared to rewarding scientific output and the quantifiable performance tasks, such as
timely delivery or number of reports [25]. Rewarding the often-invisible work on process
issues and alignment efforts as such, regardless any actual contributions to health policy,
emphasizes its importance and will motivate researchers to reflect on alignment.
Knowledge utilization will benefit from sufficient flexibility in interactions with policy-makers.
To be creative in alignment efforts and to interact with the final users of knowledge products,
researchers need a certain level of room for manoeuvre, such as time for informal meetings
and a mandate to make flexible arrangements. On the other side, organizations have to
assure the quality of their knowledge products while facing the risk of external criticism and
negative publicity. Most NPHIs will have an accredited quality system with formal operating
procedures in place for managing the risks related to quality and communication [26]. The
NPHI’s need to be flexible and creative may conflict with the need for formal procedures
to assure the quality of knowledge products from time to time. For stimulating alignment
efforts at every organizational level, we recommend NPHIs to assess regularly their internal
organizational control system, such as operating procedures and accountability rules,
specifically regarding their impact on the margin of manoeuvre for undertaking alignment
efforts by the different organizational levels.
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Related to this topic of the organizational control system, the case studies revealed that
interaction of researchers with managers and higher hierarchical levels both within the
research organization and within the commissioning organization was often limited or even
absent. Being governmental organizations, most NPHIs will be organized in a hierarchical
way with different organizational layers having a decreasing order of control from top to
bottom [27]. For each organizational layer, the mandate for taking decisions on issues will
be different as well as the importance of these issues and the considerations they attach
to them. For example, the case studies demonstrated that the researchers’ mandate for
taking decisions on data exchange with other research institutions or the strategy for
data collection was limited, which resulted in unfulfilled needs of the commissioner. The
researchers could not solve these problems on their own level, but also experienced that
it was difficult to lift the problem to a higher organizational layer [11, 12]. This lack of what
we call vertical alignment clearly hinders contributions. It was often not obvious or easy
for researchers to gain sufficient insight into the project’s context and the policy-maker’s
reality due to the information gap between the different organizational layers. Vice versa,
managers of higher organizational levels were often unaware of alignment issues at project
level. In each project, issues may arise that can better be solved in a joint endeavor across
the organization, which asks for internal, vertical alignment.
We also would like to emphasize that vertical interaction is not only relevant in case of already
existing problems. For example, we found that the way representatives of the commissioner
participate in the advisory commission of the project was indicative for their organization’s
support and use of the knowledge products afterwards (Chapter 4). Committed members
proved to be favorable for achieving contributions afterwards and we argue that vertical
alignment could also be applied for influencing the appointment of advisory-commission-
members on forehand. The need for vertical alignment during the entire process will be
obvious for major knowledge products with a presentation at the highest national level,
for example in the cases of the DHCPR and PHSF report in our study (Chapter 4 and 5). In
such cases, lack of vertical alignment may undermine alignment reached at project level,
as was the case for the PHSF report when presented to the Minister of Health. The key
message communicated by the highest management was not consistent with the message
as formulated by the researchers and aligned with the policy-makers at project level [13].
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Vertical alignment may hardly seem necessary in a project with a very specific (technical)
scope and a limited number of stakeholders as in the case study ‘Development of a Risk
Model’ (Chapter 3). However, as part of expectation management, it can be wise to verify
whether the other stakeholders also involve their management in the project outcome. Our
case studies showed that lack of vertical alignment unexpectedly led to misunderstandings
and problems in the final stage of the project.
In addition to vertical alignment on project specific issues, we argue that organizations
should also reflect on the topics alignment and alignment efforts in a systematic way on a
management level. Successful alignment efforts and valuable practices should be identified,
assured and implemented in other organization parts. For example, the double-role-actor
in the DHCPR case can be regarded as a valuable alignment practice that was not assured
by the organization. Both policy-making organizations and NPHIs should consider how to
implement a certain level of alignment assurance, for example by designating for example
by designating special alignment experts who develop alignment strategies, support their
colleagues in implementing them and who keep the organization active on alignment issues.
The two-way process
To reach alignment, efforts only from the researchers’ side will not be sufficient. We observed
that the commissioner’s efforts put into the process determine the success of a research
project to a considerable extent. Without time for consultation or possibilities to share
information, alignment with the policy-makers’ needs is very difficult to reach. In all case
studies, contact persons of the commissioning organization were very busy policy-makers
for which the commissioning a research project was an additional task to their regular
policy-making tasks. Embedding a knowledge product in a formal procedure, as is the case
for the Dutch PHSF in the public health policy cycle, increases the policy-makers’ interest
and commitment, thus stimulating their involvement in the process and their preparedness
to spend time on consultations. Furthermore, researchers can have peace of mind to some
extent about the contributions of their knowledge product to health policy since this is
largely determined by its embedding in the policy cycle. However, such a formal status is
only achievable in limited cases and for other cases, not even desirable. For example, as we
observed in the case Risk Model (chapter 3), smaller projects with experimental approaches
generating intermediate knowledge products do not serve as NPHI flagship and will have
modest contributions to policy-making. Such research projects do not easily fit into a
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predefined framework and benefit from a high degree of flexibility in the project plan. On
this level, alignment efforts nevertheless remain crucial for ascertaining commissioner’s
satisfaction since a comparative disadvantage of a less formal (and often less important)
knowledge product can be the limited commissioner’s interest and preparedness to put
efforts into the process. To overcome such situations, it is imperative that both the NPHI
and the commissioning organization commit to invest in alignment efforts. Even in case
of small projects with lesser strategic importance for the NPHI, flexible vertical alignment
should be obvious and possible. Although a modest knowledge product may not be the
most important from the NPHI’s point of view, it nevertheless contributes to its image on
the long term. For example, in the case study Risk Model (chapter 3), we found that every
(little) experience contributes to the commissioner’s view on the NPHI and may influence
future commissioning.
Next to alignment efforts, we argue that commitment to respect each other’s role in the
process is also crucial in a two-way process. On one hand, alignment with the commissioner’s
needs is necessary to get optimal contributions to policy-making. On the other hand, more
involvement of a commissioner also implies more influence on the knowledge produced
which leads us to the sensitive issue of scientific independence.
Scientific independence
To be influential in public health, a NPHI needs public trust and authoritative expertise.
Although these preconditions may seem obvious and fundamental, they are also difficult
to combine with sufficient alignment in an era of declining public trust in institutions such
as government, politics and science [28]. Most NPHIs are directly financed by their national
government, which is often also their main commissioner for several public health tasks
including research and policy advice [29]. Nowadays in the (social) media, people frequently
refer to governmental knowledge institutes as being insufficiently independent. The
authority of governmental organizations is not accepted by definition anymore and people
question the NPHI’s advices. As put forward in public discussions, some people believe that
a NPHI paid by the government will -despite of other evidence- support the governmental
position with respect to controversial public health issues such as childhood vaccination,
pollution risks and prevention measures. More than ever before, NPHIs have to balance very
sensitively and act very carefully to maintain public trust and authority [30].
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At the same time, the need to contribute to health policy is evident. NPHIs need a significant
budget raised from taxpayers, an investment which should lead to societal benefits.
Furthermore, the government considers evidence-informed (health) policy essential and
needs support to succeed in this ambition. From this perspective, the plea for better
alignment to the commissioner’s needs is fully understandable. However, the commissioner’s
involvement and interference should always be subordinate to the overriding NPHI’s need to
safeguard its scientific independence and integrity. Although no governmental organization
will contest this statement in general, the difficulty in practice lies in determining where
policy and opinions ends and science starts. Co-creation of knowledge in which researchers,
policy-makers and/or other stakeholders closely cooperate in a research project is often put
forward as desired approach to optimize alignment and to initiate knowledge use already
during the research process. However, researchers and policy-makers should be aware
that this approach may have the drawback of blurring responsibilities and jeopardizing
scientific independence. We observed that policy-makers oftentimes attempted to interfere
with scientific issues, such as the choice of methodology or definitions. The concepts
of ‘front stage work’ and ‘backstage work’ as put forward by Goffman can be helpful in
understanding and respecting each other’s role in the process [28, 31, 32]. Backstage work is
very important for alignment, as we could observe in the case studies. However, researchers
and policy-makers have to remain sufficiently autonomous and aware of their role to avoid
harm at the front stage. The challenge for researchers is to align with policy-makers and to
remain aligned while persevering in their role and discussing openly any arising tensions.
NPHIs should consider developing actively a professional attitude of their researchers in
this respect. For example, RIVM acknowledged the need to provide continuing education of
its staff in this respect by initiating the so-called ‘RIVM Academy’ in 2013, which focusses
on training researchers in the specific competences they need as experts working in a NPHI
to support the government in safeguarding public and environmental health [33]. In the
context of the Academy, they learn about the policy-making process, the commissioning
organizations and the NPHI position in society while exchanging their own experiences with
all these aspects of their work.
One should bear in mind that the NPHI’s scientific independence and integrity are
highly important: both for the NPHI itself, but also for the commissioning governmental
organizations. As mentioned before, the preconditions for reaching effective alignment and
stimulating reflection interrelate. In an organization facilitating reflection, both researchers
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and policy-makers will be able to align with each other while preserving their independence.
In the case of doubts, flexible vertical alignment supports them to find the right balance.
A delicate balance
All these considerations make clear that conducting NPHI research and producing knowledge
products in commission of governmental organizations to serve evidence-informed health
policy, is a delicate balancing act between alignment and independence, an art in itself.
One of the key tasks for a NPHI is to serve the public good by producing knowledge that
meets the needs of its commissioners. Next to ensuring a clear research question in relation
to the knowledge needs, application of a valid method and a founded interpretation of the
findings, it is the NPHI’s responsibility to present its work in a serviceable form to policy-
makers and other intended users [34]. This overall package of responsibilities, including
alignment efforts, characterizes the job of NPHI researchers. Producing knowledge to support
evidence-informed health policy in commission of governmental organizations entails an
inherent paradox making the job not that easy [3, 35]. On one hand, the commissioner asks
for answers to knowledge questions, which demands significant research efforts. At the
same time, scientific knowledge is not the only thing that matters for policy-makers; they
might disregard the knowledge at the end, despite scientific quality and all alignment efforts
put into the process [2, 35].
Furthermore, scientific knowledge will only contribute in some way to policy-making if
it fits and is included in the actor scenario of policy-makers. However, it is impossible to
know fully someone else’s actor scenario; moreover, most people are not even aware of
(all aspects of) their own actor scenario. Since actor scenarios also change continuously,
complete adaptation to someone else’s actor scenario is impossible. However, alignment is
about finding an acceptable convergence, not a pursuit of perfection. Sometimes, alignment
is even impossible despite all efforts.
Awareness of these inevitable paradoxes could be a consolation for researchers, who
experience not yielding the expected contributions to health policy. Instead, they might
consider the existence of their organization as a basic contribution to policy-making.
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In fact, the RIVM ambition to be the trusted advisor on public health and the environment is
a perfect concise formulation to describe the ideal role of NPHI researchers in policy-making
[36]. Establishing and maintaining this valuable position is more complex than one could
envisage at first sight and needs continuous efforts and evaluation of processes.
Reflection on the methodology
Reflection on the use of case studies
In this study, we conducted an evaluation of three cases from RIVM. In fact, the study can be
considered a self-evaluation, which entails both advantages and disadvantages.
Due to our existing knowledge of the organizations involved, the procedures and important
issues, we were able to conduct in-depth examinations of the cases. This proved to be very
valuable for our goal to find a practical approach for enhancing knowledge contributions.
All detailed information and insights in the different layers of a case helped us to find the
heart of the problem in alignment: effective alignment is very difficult to reach and it highly
depends on details, ongoing efforts and organizational environment.
Being aware that our bias could influence the findings, we decided to deploy independent
investigators for most interviews. Interviewees were very open and willing to provide the
interviewers with insight information, which was of great value. The processes investigated
were completed sometime before, which made us being alert on any recollection bias.
Although we cannot exclude this bias, the interviews offered so much details from
different perspectives that we were able to reconstruct a consistent picture for each case.
Furthermore, data saturation could be obtained and general issues clearly came up to the
surface, showing that many alignment areas are generally applicable. Our findings are in line
with barriers and enhancers for knowledge utilization as described in scientific literature [4,
14, 15, 18, 19, 20-23]. We therefore argue that the alignment areas defined will be relevant
for NPHIs and other knowledge institutes in the field of public health and the environment.
Since the need for a two-way process is also an important precondition, policy-makers may
also profit from the findings in their alignment efforts with research organizations.
Reflection on Contribution Mapping
In the case studies, we used Contribution Mapping as theoretical framework for our analysis.
In this paragraph, we reflect on this method.
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The Three Phase Model
In the analysis of the case studies, we considered the division of a project in three phases
very functional for our purpose to unravel alignment efforts during the project. However,
the original graphic representation of the Three Phase Model of Contribution Mapping
showing the course of a research project looks rather complicated at first sight [8]. (Figure
7.2) We experienced that the complete model is rather hard to explain to an outsider
who is not familiar with the constructivist theory. In the interviews, we used a simplified
version (without the arrows and actors) as we noticed that it was helpful for respondents in
recollecting the course of events in the project.
Figure 7.2 The Three Phase Model (Kok & Schuit, 2012 [8])
Although complicated, the model still reduces significantly the complexity of real life. In
practice, the phases of a project are not as strictly separated as the model suggests. This
specifically emerged from the feedback of the project managers during the development
of the R4P tool. Alignment needs both anticipation on coming phases and repetition of
efforts during the process. This means that most reflection questions of the R4P tool can
be relevant at any point in time. Although a division into phases is useful for retrospective
analysis, it is clearly not for reflection on alignment in practice. We decided to let go the idea
of developing separate R4P-parts in the final R4P tool. In the R4P tool, a table now indicates
the phase(s) for which every reflection question can be relevant (Chapter 6) [10].
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Analysis by Contribution Mapping
The Three Phase Model only represents the course of one project. In practice, most
researchers work simultaneously on several projects, which differ in phase, timing, size,
commissioner and structure. The same situation exists on part of the policy-makers for
whom commissioning research is often just a (minor) part of their tasks. Working on different
projects and tasks also influences alignment, if only by causing time constraints and being
engaged in inequitable issues. One could argue that the evolving actor scenarios represent
this real-life-complexity in the Three Phase Model. Nevertheless, Contribution Mapping
does not address alignment constraints related to interference of other projects or tasks.
The Contribution Mapping approach of conducting case studies, analyzing them and
providing feedback to stakeholders is laborious and asks for considerable throughput time
and research capacity. In the meantime, the projects evaluated are finished or if continued,
staffed with new researchers and policy-makers. Furthermore, the context is continuously
changing, due to reorganizations, new managers, politicians and budget considerations.
Therefore, we do not consider Contribution Mapping as an appropriate method for providing
an immediate solution to an urgent problem.
Particularly, Contribution Mapping is a valuable method for evaluating the ‘alignment
system’ of a knowledge institute. For this purpose, the method could gain strength if a
specific comparison between the intended outcome of formalized institutional procedures
and the actual outcome of all alignment efforts is also included. For example, in our case
studies, a recurrent problem reported was the gap between the formalized requirement for
researchers to align their project plan with the commissioning organization and the feasibility
to meet this requirement in the allocated period. Analysis by Contribution Mapping made
clear what the consequences of this existing gap were for the research projects. Knowledge
institute can use such general findings to optimize their internal procedures. Based on the
analysis of three cases, we were able to identify general applicable alignment areas that
are important for a NPHI, regardless the project, commissioner or people involved. By
translating these areas into the R4P tool, we made the insights of this study accessible for
interested researchers and retained them for practical use.
An important notion for applying Contribution Mapping is that it is an intervention in itself.
One should be aware that it also has the effect of an alignment effort and may change the
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constellation around the case investigated. In fact, most alignment areas mentioned in the
R4P tool also apply to a contribution-mapping project.
Reflection on the R4P tool
In this study, we developed a practical reflection tool based on our findings and intended
to support researchers in their alignment efforts. To get this tool further developed and
used by the intended users, appeared to be a case of knowledge utilization within a study
on knowledge utilization. In turn, we experienced that dissemination of our findings and
the R4P tool was likewise difficult to achieve in an effective way needing attention and
alignment efforts.
In our study, we found that alignment within the own organization is also essential. The
need for alignment exists on many levels and can hardly be underestimated. However, we
also observed that sharing of alignment experiences occurred only to a limited extent within
the organizations involved in the case studies. Again, we would like to advocate systematical
reflection and open information exchange with respect to alignment with commissioning
organizations and it would be great if this would include a certain degree of transparency
about difficult situations and mistakes to illustrate the unruly reality of reaching alignment.
Perspectives for further research
Further development of the R4P tool
In this study, we developed the R4P reflection tool for supporting NPHI researchers in
their alignment with commission governmental organizations. The tool is based on our
findings in three case studies in the health domain. In the pilot study, we demonstrated
the tool’s applicability for the health domain, but its effectiveness on actual alignment with
the commissioner needs further research. We propose to develop further the R4P tool
while using it at the same time. For this purpose, prospective action research will be most
suitable, in which researchers systematically use the tool in their project, in accordance with
a study protocol. In different cycles, in which also policy-makers should be involved and
interviewed, the researchers could implement adaptations of the tool and/or procedures
based on the findings.
As researchers suggested during the pilot study, the tool will probably be useful for
commissioning organizations too. In an implementation study, it is worthwhile to investigate
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whether applying the tool in joint meetings of researchers and commissioners could provide
a method to make implicit assumptions more explicit. If this could be achieved, alignment
and mutual trust will improve.
We hypothesize that the R4P tool will also be applicable in other research domains based
on the recognition of the R4P issues shown in different groups of researchers. Nevertheless,
a point for further development is the implementation of the R4P tool in research domains
that are linked to other commissioning ministries and/or other stakeholders than the health
domain. Such an applicability study will also show which adaptations may be needed for use
by other NPHIs.
European differences in alignment
A major challenge for NPHIs is to manage the balance between the scientific focus and the
process issues in the long term. As the case studies demonstrated and we argued before,
alignment asks for ongoing efforts and attention from researchers. The remaining question
is how to persist effectively in attention for alignment. We suggest creating an enabling
and learning organization that supports its staff in alignment efforts and process issues.
Based on the experience gained in the case studies, we expect that this will require an
integrated, long-term approach. This challenge could benefit from research on optimal
ways to preserve the motivation for process-issues and the systematic transfer of good
practices within a knowledge institute. Such research should focus on the influence of work
culture, but also on other cultural aspects in alignment. For example, in the Netherlands,
the work culture is often relatively informal in the way people interact and communicate.
The advantages of this informality are easy interaction and access to each other, but may
cover up the still existing formal hierarchy, sometimes resulting in unexpected lack of
vertical alignment. In other countries, other characteristics can be influential and it will be
useful to map these differences in future research. In the first place, this will provide insights
for enhancing contributions at a national level in the countries concerned. In the second
place, knowledge about international differences in alignment processes is highly relevant
to enhance contributions to European policy-making. It is already complex to understand
and optimize alignment processes within one country, an international context is even more
complex [37]. To complete the Dutch example, the tendency to avoid hierarchical thinking
within organizations is often reflected in the international representation of knowledge
institutes, for example in European working parties. Where the Netherlands considers
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representation by a lower hierarchical level appropriate, other member states will be more
inclined to delegate higher hierarchical levels from knowledge institutes [38], which creates
a different starting position in the consultation structure. To be aware of the implications of
these differences can be very useful for effective alignment with other member states for
realizing contributions to European policy-making.
Enhancing contributions in an era of skepticism
For this study, we focused on the level of the research project and specifically on the
researchers’ possibilities of exercising influence on their contributions to policy-making.
Our starting point was the situation where a commissioning organization has a knowledge
question and asks for scientific evidence to support the policy-making process. Even in this
situation, implying a favorable attitude towards scientific evidence, we found that alignment
is more difficult than expected, since it is about the details, ongoing attention and sticking
to one’s role. In fact, researchers have to be well acquainted with the policy-making process
and organization (and vice versa).
We also mentioned the importance of the NPHI’s scientific authority and the fact that
this authority is not as obvious anymore for the public as it used to be some decades ago.
Discussions in social media reflect public skepticism about and even denial of scientific
evidence, for example in the case of childhood vaccination and environmental change. NPHIs
already try to anticipate on this development by investigating effective risk communication
and effective participation in the public debate. However, it is also conceivable that skepticism
and denial become manifest in policies, which will be challenging to both policy-makers and
researchers, rocking the established principles in their profession [39]. Research is needed
to investigate the possible impact of this trend on enhancing knowledge contributions to
health policy and should include the level of the research project as we did in our study. The
insights gained should offer guidance for collaboration and maintaining scientific integrity,
both to researchers and to policy-makers.
Conclusions
Next to the scientific outcome, the knowledge contributions of a NPHI research project to
health policy also depend on the process, specifically the interaction between the NPHI
and the commissioning governmental organization, both at management level and at
project level. Reaching alignment with the commissioner is an important way to influence
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knowledge utilization making alignment efforts a never-ending, crucial part of a research
project. To enhance contributions to health policy, national public health institutes should
pay specific and ongoing attention to eight alignment areas: goal, tasks and authority,
quality, consultative structure, vertical alignment, organizational environment, relevance
and timing and presentation (Table 7.1). Each area represents issues that may arise in
government commissioned research. Researchers may enhance knowledge contributions
to health policy by focusing specific alignment efforts on these issues.
To identify the need for any specific alignment effort, a general rule or procedure is not
achievable since alignment depends on situation-specific details. Every research project
has its own characteristics and is constantly evolving in time. To identify the need for
specific alignment efforts, we advise researchers to reflect systematically and regularly on
the process. The reflection tool R4P, based on the important alignment areas, supports
researchers in this systematic reflection.
Nevertheless, knowledge institutes have to acknowledge that reaching alignment is much
more difficult than often believed. Furthermore, they need to balance carefully alignment
with the commissioner’s need against the institute’s scientific independence and integrity.
By organizing the institute in a way that facilitates and supports this balancing act, the NPHI
may optimize its contributions to health policy.
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13. Hegger I, Kok MO, Janssen SJ, Schuit AJ, van Oers HAM. Contributions of knowledge products to health policy: a case study on the Public Health Status and Forecasts Report 2010. Eur J Pub Health. 2016; 26(6):922-927.
14. De Leeuw E, McNess A, Crisp B, Stagnitti K. Theoretical reflections on the nexus between research, policy and practice. Crit Public Health 2008;18:5–20
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17. Wehrens R. Beyond two communities -from research utilization and knowledge translation to co-production?PublicHealth.,2014;128(6):545-551.
18. Strydom WF, Funke N, Nienaber S, Nortje K, Steyn M. Evidence-based policymaking: A review. S Afr J Sci 2010;106(5/6):249.
19. Sedlačko M, Staroňová K. An Overview of Discourses on Knowledge in Policy: ThinkingKnowledge, Policy and Conflict Together. Cent Eur J Public Health. 2016; 9(2): 10-31.
20. Keijsers JFEM, Paulussen TGWM, Peters LWH, Fleuren MAH, Lammers F. Better use of knowledge: Information behaviour of national policy makers. (In Dutch: Kennis beter benutten: Informatiegedrag van nationale beleidsmakers). Woerden: NIGZ and TNO; 2005.
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22. Haynes AS, Derrick GE, Chapman S, Redman S, Hall WD, Gillespie J, Sturk, H. From “our world” to the “real world”: Exploring the views and behaviour of policy-influential Australian public health researchers. Soc Sci Med. 2011; 72(7):1047-1055.
23. Kothari A, Birch S, Charles C. “Interaction” and research utilisation in health policies and programs:doesitwork?HealthPolicy.2005;71(1):117-125.
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25. Frey BS, Homberg F, Osterloh M. Organizational Control Systems and Pay-for-Performance in the Public Service. Organization Studies. 2013; 34(7): 949-972.
26. Viso AC, Wanoyoike S, Dusenbury C, Mably S, Sethi M, Desenclos JC. Peer-to-Peer Evaluation Initiative for National Public Health Institutes. In: A Series of Technical and Policy Briefs. 2014; IANPHI: St-Maurice, France; Atlanta, USA.
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29. IANPHI. The International Association of Public Health Institutes. Available from: http://www.ianphi.org/. Accessed: 15 January 2017.
30. Assmuth T, Lyytimäki J. Co-constructing inclusive knowledge within converging fields: Environmental governance and health care. Environ. Sci. Policy 2015 51: 338-350.
31. Goffman E. The presentation of self in everyday life. London: Penguin; 1990.32. Bekker M, van Egmond S, Wehrens R, Putters K, Bal R. Linking research and policy in Dutch
healthcare: infrastructure, innovations and impacts. Evid Policy 2010;6(2):237–253.33. RIVM. Annual Report 2013: RIVM Academy encourages learning. Bilthoven: RIVM. Available
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38. Nederlandse END-vereniging. Handleiding voor Nederlandse Gedetacheerde Nationale Deskundigen (In English: Manual for seconded national experts). 2013. Available from: http://eu.nlvertegenwoordiging.org/binaries/content/assets/postenweb/b/belgie/permanente-vertegenwoordiging-van-nederland-bij-de-eu-in-brussel-pv-eu/import/europese_instellingen/end/handleiding_end/handleiding---update---end-najaar-2013.pdf. Accessed: 15 January 2017.
39. Lewandowsky S, Mann ME, Brown NJL, Friedman H. Science and the Public: Debate, Denial, and Skepticism. Journal of Social and Political Psychology, North America, 4, Aug 2016. Available at: http://jspp.psychopen.eu/article/view/604. Date accessed: 12 March 2017.
Summary
Samenvatting
Dankwoord
About the author
ListofPublications(2011-2017)
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Summary
Chapter 1. Introduction
In this thesis, we describe an empirical study on how contributions of knowledge and
knowledge products to health policy-making are achieved. We have investigated how these
contributions can be enhanced by focusing on the processes involved in the relationship
between research and health policy-making and by taking into account the continuously
changing context of the research process.
We specifically addressed the use of knowledge produced by knowledge institutes, such as
National Public Health Institutes (NPHIs), in public policy by governmental organizations.
These knowledge institutes weigh and translate relevant information for the purpose of
policy-making and often present the knowledge in a way that meets the needs of the
policy-makers, in the form of reports, tools, websites, infographics, or other knowledge
products. In practice, NPHI researchers experience that knowledge contributions to policy-
making are not self-evident and despite taking into account the policy-makers’ needs,
contributions of knowledge products to health policy are difficult to achieve. In the pursuit
of evidence-informed health policy-making, decision-making is well informed by the best
available research evidence and scientific knowledge. However, one should bear in mind
that other types of information, such as ideas and interests, are also relevant and influential
in addressing the wicked problems in public health and health care. When NPHI researchers
intend to contribute effectively to policy-making, they will need some insights on knowledge
utilization in policy-making and support in the form of practical tools next to their specific
scientific expertise.
The aim of this study was to obtain insights in how knowledge institutes such as NPHIs can
enhance the contributions to evidence-informed health policy of knowledge produced in
commission of governmental organizations. We addressed the following research questions:
1. What alignment areas are important for enhancing the contributions to health
policy of government commissioned research commissioned by National Public
HealthInstitutes?
2. Based on the empirical findings gained in this study, what is a practical approach to
enhance knowledge contributions from NPHIs to evidence-informed health policy-
makingatnationallevel?
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For this study, Contribution Mapping provided the theoretical framework. We used a case
study approach and mapped in detail the process of three projects of the Dutch National
Institute for Public Health and the Environment (RIVM), focusing on the alignment efforts in
the projects and the projects’ contributions to health policy-making by the commissioner at
national level. Based on the findings from the case studies, we identified the most decisive
alignment areas for optimal knowledge contributions to health policy-making. Finally, we
prepared and evaluated a draft tool based on the theoretical framework and empirical
findings for supporting researchers in alignment.
Chapter 2. The complex relationship between research and health policy: a concise
overview of theoretical approaches
It often appears difficult to achieve integration of scientific knowledge and research
evidence into health policy; a problem which has been subject of extended scientific
research in social sciences for several decades. Chapter 2 provides a concise overview of the
theoretical background for the complex relationship between research and health policy,
which describes an influential typology of knowledge use and successive theoretical models
on knowledge utilization.
Knowledge can be used in different ways and Weiss provided an influential typology of
knowledge use, which makes a division between instrumental, conceptual and symbolic use
of knowledge. Instrumental use means that technical, objective data are utilized in a direct,
specific way to solve a particular problem. Conceptual use emerges when research delivers
ideas to policy-makers, which changes their perception of a problem. When decision makers
use research as an argument to take an advocacy position, it influences policy in a symbolic
way.
To handle the complexity of knowledge utilization, models have been developed to explain
actual knowledge use and to identify barriers and enhancers to improve the knowledge
utilization. The rational positivist models regard knowledge as a product for use in policy-
making at a certain point in time. These models presume two different worlds of science
and policy-making and hardly reflect the complex and incremental nature of policy-making.
Interactive models of science-policy relations also consider the context, communication
and interaction between researchers and policymakers for bridging the gap between the
two communities. Constructivist models emphasize the co-creation of knowledge in a
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social process and consider boundaries between research and policy as the outcome of
negotiation processes between researchers and policy-makers. The idea of separate
worlds is replaced by the concept of ‘hybrids’ where researchers and policy-makers co-
create knowledge in mutual interaction. In this concept, boundary organizations having
characteristics of both science and politics, and involving both scientists and policy-makers
in knowledge production, can play an important role. In a negotiation process including
informal interaction, researchers and policy-makers search for consensus backstage behind
the scenes. This boundary work creates trust and makes knowledge (products) ‘acceptable’
at the formal frontstage, where a clear division of tasks and responsibilities is presented to
the public.
All models offer some part of understanding about what is going on in the relationship
between science and policy and the different theoretical approaches resulted in different
practices to improve knowledge utilization. The positivist approach is reflected in knowledge
translation activities such as research priority setting, knowledge distribution and evaluation
of uptake. From the interaction perspective, knowledge brokers linking researchers and
knowledge users act as valuable intermediates to bridge the gap between the two worlds. In
this study, we used the Contribution Mapping approach by Kok and Schuit, a constructivist
approach for monitoring research projects and for understanding of how to improve
alignment between researchers and knowledge users. Contribution Mapping introduces the
concept of alignment efforts, which are efforts undertaken by researchers and other involved
actors, such as commissioner and knowledge users, to reach alignment in the research
process. Alignment efforts are the starting point for enhancing research contributions to
policy-making and have a central role in this study. Furthermore, the term actor scenario
indicates the involved actors’ scenario of the future. According to Contribution Mapping,
knowledge has to feature in the actor scenario of (intended) knowledge users for achieving
actual contributions.
Chapter 3. Analyzing the contributions of a government-commissioned research project:
a case study
Chapter 3 describes the first case study ‘Development of a Risk Model’, in which we analyzed
the process of an RIVM project. In this project, risk-ranking models for clinical trials were
developed in commission of the Health Care Inspectorate. The aim of our case study was
to identify the alignment efforts that influenced contributions of the Risk-Model-project to
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the Inspectorate’s work. According to the Contribution Mapping approach, we conducted
an analysis of relevant documents such as minutes of project meetings and we interviewed
actorsfromRIVMandInspectorateinvolvedintheproject(n=10):theRIVMinvestigators,
the key users of the risk models (four inspectors) and managers from both RIVM and the
Inspectorate at two different organization levels. In a feedback session with inspectors,
RIVM investigators and their managers, we discussed our findings for finalization. Based on
the findings, we inductively identified six categories of relevant alignment efforts.
We found that both organizations, RIVM and Inspectorate, had divergent views on the
ownership of the project’s knowledge products and on the mutual relationship of their
organizations, which resulted in different expectations with respect to the project. The
RIVM researchers considered the use of the risk models to be disappointing, whereas
the inspectors had a positive opinion about their contributions. However, all interviewed
actors (investigators, inspectors, and managers) were unaware of these remarkably
different perceptions. We identified six relevant categories of alignment efforts: relevance,
consultative structure, goal and timing, tasks and authority, vertical alignment and
organizational environment. These six categories of alignment efforts include both horizontal
alignment efforts between the investigators and inspectors as well as vertical alignment
efforts between investigators or inspectors and their managers within the own organization.
Furthermore, it became manifest that alignment efforts can be relevant at three levels: at
the first level, to align between investigators and linked actors; at the second level, to achieve
alignment with the organizational environment of the project; at the third level, to align
between the involved organizations as part of their formal and historical relationship (existing
irrespective of the project). Researchers can improve first-level alignment by continuous
reflection on the process, awareness of mutual expectations, and open discussions with the
commissioner. At the second level, vertical alignment is essential to formulate an adequate
response to challenges for the research project from the organizational environment.
Alignment at the third level is more difficult to influence and requires a collective approach
at all organizational levels.
Based on the findings in this first case study, the importance of a reflective attitude towards
the social aspects of research projects at all levels of the organization became clear.
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Chapter 4. Enhancing the contributions of research to health care policy-making: a case
study on the Dutch Health Care Performance Report
In a second case study, we analyzed the developmental process of the 2010-edition of the
Dutch Health Care Performance Report (DHCPR). The DHCPR is a major RIVM knowledge
product, in which the health care performance in the Netherlands is monitored by using
indicators for quality, accessibility and affordability of health care. Both RIVM and the
Ministry of Health wishes to increase the contribution of the DHCPR to health care policy-
making and our aim was to identify ways to achieve that. This case study focused specifically
on the process at project level, where RIVM researchers and policy-makers of the Ministry
of Health are the main involved actors. To investigate which areas need specific alignment
efforts by researchers and/or policy-makers to enhance the contributions of the DHCPR, we
interviewedRIVMresearchers(n=8)andpolicy-makersfromtheMinistryofHealth(n=10).
We integrated the interview data with findings from the document analysis of relevant
(policy) documents and reports and assessed the process for developing the 2010 version of
DHCPR according to the Contribution Mapping approach.
We identified six areas where alignment is specifically relevant for enhancing the
contributions of future versions of the DHCPR. These areas are:
1. the DHCPR content for presenting well-balanced information for different
ministerial directorates;
2. backstage work for negotiating the border between science and policy-making and
for reaching consensus on the formulation of findings and recommendations;
3. availability of double role actors working both at the knowledge institute and the
Ministry for enhancing information exchange and mutual understanding;
4. (expected) reports of other knowledge institutes for avoiding overlap, contradictions
and poor timing;
5. data collection and generation for assuring data completeness and continuity of
data supply.;
6. the form in which project results are presented for being aligned to the needs of
the end users and the commissioner
We found that achieving the contribution of healthcare-performance-reporting to policy-
making is complicated and requires continuous alignment efforts between researchers and
policy-makers. These efforts should therefore form an inseparable part of the healthcare-
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performance-reporting. This demands substantial resources, but it is worth considering
since it may pay back in better contributions to policy-making.
Chapter 5. Contributions of knowledge products to health policy: a case study on the
Public Health Status and Forecasts Report 2010
Chapter 5 describes the case study on the 2010-edition of the Dutch Public Health Status
and Forecasts report (PHSF 2010). The PHSF Report integrates research data on public
health and identifies future trends affecting public health in the Netherlands. The PHSF has
a formalized position in the national public-health policy cycle and is issued by RIVM every
four years. RIVM considers all policy-makers at the Ministry of Health, Welfare and Sport its
key users, but RIVM-researchers experience that far from all policy-makers are familiar with
the PHSF and that the group of users could considerably be extended.
To investigate how PHSF contributions to national health policy can be enhanced, we
analyzed the development process of the PHSF 2010. As in the previous two case studies,
we used Contribution Mapping in this case. For collecting data, this study included the
analysis of documents from the PHSF-2010 process and in-depth semi-structured interviews
with key actors from RIVM and the Ministry of Health who were involved in VTV 2010.
Interviewers independent from RIVM and the Ministry of Health conducted the interviews
withRIVM researchers andmanagers at three levels (n=10) andwith policy-makers and
managersatthreelevelsattheMinistryofHealth(n=10).Finally,weidentifiedimportant
areas for alignment efforts using a constant comparative analysis method.
The PHSF report is considered an example of successful boundary work in literature. Indeed,
the PHSF-2010 process included several established activities aiming at alignment between
researchers and policy-makers, such as informal meetings. Nevertheless, we identified
three issues that are easily overlooked in knowledge development, but provide suggestions
for enhancing contributions to health policy. The first issue is awareness of divergent and
continuously changing actor scenarios; the second issue is attention for effective vertical
alignment within the organizations involved; and the third issue is attention for careful
timing of draft-knowledge-products to create early adopters. We found that it is insufficient
to raise the awareness of potential new users to enhance the contributions made by an
established public health report, such as the PHSF Report. This is because the knowledge
product must also be geared to the needs of new users and must be introduced into the
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scenarios of new actors who may be less familiar to the researchers. However, in order to
keep established users on board, the demand for knowledge product adaptations has to be
carefully considered. This requires continuous alignment efforts in all directions: horizontal
and vertical, external and internal.
Chapter6.ResearchforPolicy(R4P):Developmentofareflectiontoolforresearchersto
improve knowledge utilization
In the three previous chapters, we extensively evaluated complex research projects
commissioned by the Ministry of Health to investigate how alignment is achieved in a
research process and to discover ways to enhance knowledge contributions to health
policy. We found that alignment between researchers and policy-makers during knowledge
production is essential, but difficult to maintain. In this chapter, we describe how the
findings of the three case studies were integrated into a practical tool for researchers to
enhance their contribution to evidence-informed policy.
By cross-case analysis of the three case studies, we identified the following eight important
alignment areas:
1. Goal of the project;
2. Tasks and authorities of involved actors;
3. Quality of the research method;
4. Consultative structure in the project;
5. Vertical alignment within organizations;
6. Organizational environment of the project;
7. Relevance and timing of knowledge products;
8. Presentation of research findings.
Since we found that alignment between research and policy-making requires continuous
efforts and a clear understanding of process issues in the research project, we prepared a
tool for supporting researchers in their alignment efforts. Our starting point was that we
want to encourage researchers to reflect on process issues in order to become aware of any
need for alignment.
In an iterative process, we developed a tool that includes practical reflection questions for
researchers taking into account the eight alignment areas. This Research for Policy (R4P) tool
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was tested with input from the RIVM project managers of three new research projects in
2015. They regarded the R4P tool as a useful checklist for alignment in a research project.
Based on their feedback, illustrative examples from the case studies were added to the
reflection questions. The project managers suggested making the tool accessible not only
to researchers but also to policy-makers. We adjusted the format of the R4P tool further to
the users’ needs by adding clickable links. In this way, the R4P tool offers practical alignment
guidance and facilitates reflection on process issues, which supports researchers in aligning
with policy-makers and in acting in a context-sensitive way.
Chapter 7. Discussion and Conclusion
In this chapter, the study as a whole is discussed including a reflection on the findings in
relation to the research questions and on the methods applied. Finally, it provides some
perspectives for further research and ends with the conclusion of this study.
The findings of the three case studies (chapter 3, 4 and 5) and the cross-case analysis
(chapter 6) provided an answer to the first research question:
What alignment areas are important for enhancing the contributions to health policy of
government commissioned research commissioned by National Public Health Institutes?
From the case studies, we identified eight alignment areas that need specific attention
to prevent unaligned situations during the research project (chapter 6). These areas are
consistent with critical factors for knowledge utilization mentioned in scientific literature.
However, another crucial finding is that reaching alignment in practice turns out to be very
difficult. It requires ongoing attention to details and awareness of the critical factors, for
knowledge about the other stakeholders’ concerns and for political sensitivity. This causes
alignment efforts to be much more time-consuming than anticipated and researchers need,
apart from enthusiasm for scientific issues, enthusiasm for process issues in order to sustain
in conducting alignment efforts.
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The second research question was:
Based on the empirical findings gained in this study, what is a practical approach to enhance
knowledge contributions from NPHIs to evidence-informed health policy-making at national
level?
From the case studies, we learned that effective alignment needs continuous reflection
on the process. We developed a reflection tool, called R4P tool, for making the findings
available for researchers in a practical way and offering them support in determining
the type and intensity of the alignment efforts needed (chapter 6). Nevertheless, we
argue that the R4P tool can only be effectively used in an organizational framework that
meets some preconditions. Since continuous attention for process issues is difficult to
sustain, researchers need support in reflection and alignment efforts. The most important
preconditions for sufficient alignment are (1) a facilitating organization, (2) alignment as a
two-way process and (3) the right balance between scientific independency and alignment
with the commissioner’s needs.
A facilitating organization of a knowledge institute rewards not only scientific achievements,
but also alignment efforts for ensuring a smooth process, since this motivates researchers
to spend time and energy to this often-invisible part of their job. Furthermore, alignment
benefits from flexibility in interactions of researchers with policy-makers, which implies
that the margin of manoeuvre for undertaking alignment efforts has to be sufficient for all
organizational levels. For knowledge institutes, vertical alignment should be an important
point of concern since we found that lack of it clearly hinders knowledge contributions. In
addition, both policy-making organizations and NPHIs should consider how to implement
a certain level of alignment assurance by their organization, for example by designating
special alignment experts who develop alignment strategies, who support their colleagues
in implementing them and who keep the organization active on alignment issues.
Reaching alignment needs a two-way process. For an optimal outcome, both the NPHI and
the commissioning organization should spend time and energy to the process and commit
to invest in alignment efforts. We observed that for a knowledge product embedded in a
formal procedure, as is the case for the PHSF report, commitment to the process increases
at both the NPHI and the governmental commissioning organization. Nevertheless, small
projects with lesser strategic importance also need two-way alignment efforts at different
organizational levels since they all contribute to the relationship between NPHI and
commissioning organization in the long term.
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Alignment with the commissioner’s needs to get optimal contributions to policy-making
may apparently conflict with the NPHI’s scientific independence. Nowadays, the authority
of governmental organizations is not accepted by definition anymore and people publicly
question the NPHI’s advices, for example on vaccination. The challenge for researchers is
to align with policy-makers and to remain aligned while persevering in their independent
scientific role and not creating any alleged conflict of interest. NPHIs should therefore
support their staff in developing the specific skills needed for working at this nexus of
science and health policy.
In this study, we used a qualitative case study approach that enabled an in-depth examination
of the cases. For data analysis, the Contribution Mapping approach offered a functional
three-phase model to unravel alignment efforts. During the development of the R4P tool,
it became clear that the reflection questions for the three different phases showed overlap
and needed to be largely identical. The final R4P tool is therefore organized by process topics
instead by the three phases of the research process. We consider Contribution Mapping
a valuable method for evaluating the alignment system of a knowledge institute, since it
reveals institutional patterns to be tackled. Since the method requires much time and effort,
using it for the evaluation of a small project will be less obvious.
Perspectives for further research include further development of the R4P tool, European
differences in alignment and the implications of skepticism towards science. The R4P tool
has to be validated for alignment-outcome and can be extended to other research domains.
For operating in European and international networks, it is useful to investigate whether
cultural differences between countries affect alignment and alignment efforts. These
insights can be used to improve the contribution of scientific knowledge to health policy at
international level.
Based on our study, we argue that knowledge institutes have to acknowledge that reaching
alignment needs much more effort, time and resources than often presumed. Conducting
research at an NPHI and generating knowledge products in commission of governmental
organizations to serve evidence-informed health policy is a delicate balancing act between
alignment and independence. By organizing the institute in a way that facilitates and
supports this balancing act, the NPHI may optimize its contributions to health policy.
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Samenvatting
Hoofdstuk 1. Inleiding
In dit proefschrift beschrijven we een empirische studie over hoe bijdragen van
wetenschappelijke kennis aan gezondheidsbeleid tot stand komen. We hebben onderzocht
hoe deze bijdragen kunnen worden versterkt door gerichte aandacht voor de processen die
plaatsvinden in de relatie tussen onderzoek en beleidsvorming en door rekening te houden
met de steeds veranderende context van het onderzoeksproces.
We hebben ons specifiek gericht op het gebruik van kennis die wordt geproduceerd ten
behoeve van het nationale overheidsbeleid door kennisinstituten, zoals de nationale
volksgezondheidsinstituten (NPHIs; National Public Health Institutes in het Engels). Dergelijke
kennisinstituten integreren en duiden relevante informatie voor beleidsontwikkeling
en presenteren vervolgens deze kennis meestal op een wijze die tegemoet komt aan de
behoeften van de beleidsmakers, in de vorm van rapporten, instrumenten, websites,
infographics, of andere kennisproducten. In de praktijk ervaren de onderzoekers echter dat
het gebruik van de door hun geleverde kennis bij de beleidsvorming niet vanzelfsprekend
is, ondanks dat rekening is gehouden met de specifieke kennisbehoeften van de
beleidsmakers. De overheid streeft weliswaar naar zogenaamde ‘evidence-informed health
policy-making’, waarbij in de besluitvorming de beste beschikbare onderzoeksgegevens
en wetenschappelijke kennis worden betrokken, maar het is daarnaast belangrijk om in
gedachten te houden dat ook andere soorten informatie dan wetenschappelijke kennis,
zoals ideeën, belangen en praktijkervaring, relevant en invloedrijk zijn bij het aanpakken
van complexe en vaak hardnekkige problemen in de volksgezondheid en gezondheidszorg.
Wanneer NPHI-onderzoekers effectief willen bijdragen aan beleidsontwikkeling, hebben
ze, naast hun specifieke wetenschappelijke expertise, ook inzicht in kennisgebruik bij
beleidsvorming nodig en ondersteuning in de vorm van praktische hulpmiddelen.
Het doel van deze studie was om inzicht te verkrijgen in hoe kennisinstituten, zoals NPHIs, de
bijdragen van de kennis geproduceerd in opdracht van overheidsorganisaties aan evidence-
informed beleid kunnen versterken. Hiervoor hebben we de volgende onderzoeksvragen
geformuleerd:
1. Welke afstemmingsgebieden zijn belangrijk om de bijdragen aan gezondheidsbeleid te
versterken van projecten uitgevoerd door NPHIs in opdracht van de overheid?
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2. Op basis van de empirische bevindingen van deze studie, wat is een praktische aanpak om
kennisbijdragen van NPHI’s aan evidence-informed gezondheidsbeleid op nationaal niveau
te verbeteren?
Voor deze studie leverde Contribution Mapping het theoretische kader. We hebben
casestudies uitgevoerd, waarin we gedetailleerd het proces van drie projecten van het
Nederlandse Nationaal Instituut voor Volksgezondheid en Milieu (RIVM) in kaart hebben
gebracht en vooral aandacht hebben besteed aan de inspanningen om af te stemmen
(alignment efforts) in de projecten en de bijdragen (contributions) van de projecten aan
het gezondheidsbeleid op nationaal niveau. Op basis van de bevindingen uit de casestudies
hebben we vastgesteld wat de belangrijkste onderwerpen zijn om over af te stemmen als
je een optimale bijdrage van kennis aan gezondheidsbeleid wilt bereiken. Op basis van
het theoretische kader en de empirische bevindingen, hebben we tot slot een concept-
instrument dat tot doel heeft onderzoekers te ondersteunen in het afstemmen, ontwikkeld
en geëvalueerd.
Hoofdstuk 2. De complexe relatie tussen onderzoek en gezondheidsbeleid: een beknopt
overzicht van theoretische benaderingen
Het blijkt vaak moeilijk om te bewerkstelligen dat wetenschappelijke kennis en bewijs
uit onderzoek daadwerkelijk in gezondheidsbeleid verwerkt worden: een probleem dat
al jarenlang het onderwerp is van uitgebreid wetenschappelijk onderzoek in de sociale
wetenschappen. Hoofdstuk 2 geeft een beknopt overzicht van de theoretische achtergrond
voor de complexe relatie tussen onderzoek en gezondheidsbeleid, waarin we een invloedrijke
typologie van kennisgebruik en opeenvolgende theoretische modellen over kennisgebruik
beschrijven.
Kennis kan op verschillende manieren gebruikt worden. Weiss heeft een invloedrijke
typologie van kennisgebruik geformuleerd, waarin instrumenteel, conceptueel en symbolisch
gebruik van kennis worden onderscheiden. Instrumenteel gebruik betekent dat technische,
objectieve gegevens op een directe, specifieke manier worden gebruikt om een probleem
aan te pakken. Conceptueel gebruik komt tot stand wanneer onderzoek aanleiding geeft tot
nieuwe denkbeelden bij beleidsmakers en zo hun perceptie van een probleem verandert.
Wanneer bij een beslissing of in een discussie onderzoek gebruikt wordt als argument voor
een bepaald standpunt, beïnvloedt onderzoek het beleid op een symbolische manier.
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Om de complexiteit van kennisgebruik te kunnen hanteren, zijn modellen ontwikkeld om
het daadwerkelijke kennisgebruik te verklaren en barrières en bevorderende factoren voor
kennisgebruik te identificeren. De rationele positivistische modellen beschouwen kennis als
een product voor gebruik in beleidsontwikkeling op een specifiek moment. Deze modellen
veronderstellen twee verschillende werelden van wetenschap en beleidsontwikkeling en
weerspiegelen nauwelijks de complexe en incrementele aard van beleidsontwikkeling.
Interactieve modellen van de relatie wetenschap-beleid houden echter ook rekening met
de context, communicatie en interactie tussen onderzoekers en beleidsmakers om de kloof
tussen de twee gemeenschappen te overbruggen. Constructivistische modellen benadrukken
de co-creatie van kennis in een sociaal proces en beschouwen de grens tussen onderzoek
en beleid als de uitkomst van de onderhandeling die plaatsvindt tussen onderzoekers en
beleidsmakers. Het idee van afzonderlijke werelden is hierbij vervangen door hybride
ruimtes waarin onderzoekers en beleidsmakers in wederzijdse interactie kennis creëren.
In dit concept kunnen zogenaamde boundary organizations, die zowel wetenschappelijke
als beleidsmatige kenmerken hebben en zowel wetenschappers als beleidsmakers in de
kennisproductie betrekken, een belangrijke rol spelen. Achter de schermen (backstage)
wordt in een onderhandelingsproces met informele contacten tussen onderzoekers en
beleidsmakers gezocht naar consensus, ook wel boundary work genoemd. Zo wordt
vertrouwen gecreëerd en worden kennis en kennisproducten acceptabel gemaakt voor het
formele openbare podium (front stage) waar een duidelijk onderscheid bestaat in taken en
verantwoordelijkheden van onderzoek en beleid.
Alle modellen bieden op een andere manier inzicht in de relatie tussen wetenschap en
beleid en de verschillende theoretische benaderingen hebben geleid tot verschillende
benaderingen om kennisgebruik te verbeteren. De positivistische aanpak wordt weerspiegeld
in kennistranslatie-activiteiten zoals het opstellen van onderzoeksagenda’s, disseminatie
van kennis en evaluatie van gebruik en toepassing. Vanuit het interactieperspectief fungeren
kennismakelaars die onderzoekers en kennisgebruikers met elkaar in contact brengen
en verbinden, als waardevolle tussenpersonen om de kloof tussen de twee werelden te
overbruggen. In deze studie hebben we Contribution Mapping van Kok en Schuit gebruikt,
een constructivistische benadering om het proces van onderzoeksprojecten te analyseren
en inzicht te krijgen in de mogelijkheden om de afstemming tussen onderzoekers en
kennisgebruikers te verbeteren. Contribution Mapping gebruikt de term alignment
efforts voor de inspanningen van betrokkenen om tot onderlinge afstemming in het
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192 | Samenvatting
onderzoeksproces te komen. Alignment efforts is ook de term die we in deze Nederlandstalige
samenvatting hanteren: ze vormen het aanknopingspunt om de bijdragen van onderzoek
aan beleidsontwikkeling te verbeteren en hebben een centrale plaats in deze studie. Verder
wordt de term actorscenario gebruikt om het toekomstscenario van betrokkenen (actoren)
aan te duiden. Volgens Contribution Mapping kan kennis pas daadwerkelijk een bijdrage
leveren als het een plek krijgt in het actorscenario van (beoogde) kennisgebruikers.
Hoofdstuk 3. Analyse van de bijdragen van een onderzoeksproject uitgevoerd in opdracht
van de overheid: een casestudie
Hoofdstuk 3 beschrijft de eerste casestudie waarin we het onderzoeksproces van het RIVM-
project ‘Ontwikkeling van een risicomodel’ analyseren. In dit risicomodelproject werden in
opdracht van de Inspectie voor de Gezondheidszorg modellen ontwikkeld voor het scoren
van risico’s van klinische studies. Het doel van onze casestudie was om de alignment efforts
te identificeren die de bijdrage van het risicomodelproject aan de werkzaamheden van de
inspectie hebben beïnvloed. In lijn met de Contribution Mapping werkwijze hebben we een
analyse uitgevoerd van relevante documenten zoals de verslagen van projectbijeenkomsten.
Vervolgens hebben we interviews gehouden met actoren van RIVM en inspectie, die
betrokkenwarenbijhetproject(n=10):ditwarendeRIVM-onderzoekers,debelangrijkste
gebruikers van de risicomodellen (vier inspecteurs) en de managers van zowel RIVM als de
inspectie op twee verschillende organisatieniveaus. In een feedbacksessie met inspecteurs,
RIVM-onderzoekers en hun managers hebben we onze bevindingen besproken om de
casestudie af te ronden. Op basis van de bevindingen hebben we op inductieve wijze zes
categorieën relevante alignment efforts geïdentificeerd.
We stelden vast dat beide organisaties, RIVM en inspectie, een andere visie hadden op het
eigenaarschap van de kennisproducten van het risicomodelproject en op de onderlinge
relatie tussen hun organisaties, hetgeen resulteerde in uiteenlopende verwachtingen over
het project. De RIVM onderzoekers vonden het gebruik van de risicomodellen teleurstellend,
terwijl de inspecteurs juist positief waren over de bijdragen van de risicomodellen. Alle
geïnterviewde betrokkenen (onderzoekers, inspecteurs en hun managers) waren zich
echter van deze opmerkelijke verschillen in beleving niet bewust. We vonden zes relevante
categorieën alignment efforts: relevantie, overlegstructuur, doel en timing, taken en
zeggenschap, verticale afstemming en organisatorische omgeving. Deze belangrijke
categorieën alignment efforts omvatten zowel horizontale alignment efforts tussen de
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onderzoekers en de inspecteurs, als verticale alignment efforts tussen onderzoekers dan
wel inspecteurs en hun managers binnen de eigen organisatie.
Het werd bovendien duidelijk dat alignment efforts van belang zijn op drie niveaus.
Op het eerste niveau gaat het om afstemming tussen de onderzoekers en andere direct
betrokkenen bij het project; op het tweede niveau om afstemming vanuit het project op de
organisatorische omgeving; op het derde niveau gaat het om afstemming tussen de twee
betrokken organisaties als onderdeel van hun formele en historische relatie (die ongeacht het
project bestaat). Onderzoekers kunnen de afstemming op het eerste niveau zelf verbeteren
door regelmatig te reflecteren op het proces, door zich bewust te zijn van de wederzijdse
verwachtingen en door open gesprekken met de opdrachtgevers. Op het tweede niveau is
verticale afstemming essentieel om adequaat te kunnen reageren op uitdagingen voor het
onderzoeksproject vanuit de organisatorische omgeving. Afstemming op het derde niveau is
lastiger te beïnvloeden en vereist een collectieve aanpak van alle organisatorische niveaus.
Uit de bevindingen van deze eerste casestudie werd het belang duidelijk van een
reflecterende houding op alle niveaus van de organisatie ten opzichte van de sociale kant
van onderzoeksprojecten.
Hoofdstuk 4. Verbeteren van de bijdrage van onderzoek aan gezondheidszorgbeleid: een
casestudie over de Nederlandse Zorgbalans
In een tweede casestudie hebben we het ontwikkelingsproces geanalyseerd van de
2010-editie van de Zorgbalans. De Zorgbalans is een belangrijk RIVM kennisproduct dat
rapporteert over de gezondheidszorgprestaties in Nederland op basis van indicatoren voor
de kwaliteit, de bereikbaarheid en de betaalbaarheid van de gezondheidszorg. Zowel het
RIVM als het Ministerie van Volksgezondheid, Welzijn en Sport (VWS) wil de bijdrage van de
Zorgbalans aan het gezondheidszorgbeleid versterken en het doel van deze casestudie was
manieren te identificeren om dit te kunnen bereiken. De casestudie richtte zich specifiek op
het proces dat op projectniveau plaatsvindt, waarin RIVM-onderzoekers en beleidsmakers
van het Ministerie van VWS de belangrijkste betrokkenen zijn. Om te onderzoek welke
aandachtsgebieden specifieke alignment efforts van onderzoekers en / of beleidsmakers
nodig hebben om de Zorgbalans-bijdrage aan beleid te versterken, hebben we RIVM-
onderzoekers(n=8)enbeleidsmakersvanhetMinisterievanVWS(n=10)geïnterviewd.De
interviewgegevens hebben we vervolgens geïntegreerd met bevindingen uit de analyse van
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relevante (beleids)documenten. Daarna hebben we het ontwikkelingsproces van Zorgbalans
2010 geanalyseerd volgens de Contribution Mapping aanpak.
We hebben zes aandachtsgebieden geïdentificeerd waar afstemming specifiek van belang
is om voor nieuwe edities van de Zorgbalans de bijdrage aan beleid te verbeteren. Dit zijn:
1. de inhoud van de zorgmonitor om de informatie goed uit te balanceren voor de
verschillende directoraten op het Ministerie van VWS;
2. het zogenaamde ‘backstage’-werk, om achter de schermen over de grens tussen
wetenschap en beleid te onderhandelen en informeel te kunnen zoeken naar
consensus;
3. de beschikbaarheid van medewerkers die zowel in het onderzoeksinstituut als het
ministerie werken (double-role-actors) om zo de uitwisseling van informatie en het
wederzijds begrip te versterken;
4. de (te verwachten) rapporten van andere kennisinstellingen om overlap,
tegenspraak en ongelukkige timing te voorkomen;
5. dataverzameling en datageneratie zodat de volledigheid van data en de continuïteit
van datatoelevering geborgd zijn;
6. de wijze waarop de projectresultaten worden gepresenteerd zodat het aansluit bij
de behoeften van de eindgebruikers en de opdrachtgever.
We hebben geconstateerd dat de totstandkoming van de bijdrage aan beleid van een
zorgmonitor ingewikkeld is en dat onderzoekers en beleidsmakers daarvoor voortdurend
moeten afstemmen. Alignment efforts moeten daarom een onlosmakelijk onderdeel
vormen van de ontwikkeling van een zorgmonitor. Dit vergt wel een substantieel deel van
het budget, maar is het overwegen waard omdat het zich terugbetaalt in een betere bijdrage
aan beleid.
Hoofdstuk 5. De bijdrage van kennisproducten aan gezondheidsbeleid: een casestudie
over de Volksgezondheid Toekomst Verkenning 2010
Hoofdstuk 5 beschrijft de casestudie over de Volksgezondheid Toekomst Verkenning (VTV)
van 2010. De VTV integreert onderzoeksgegevens over publieke gezondheid en identificeert
toekomstige trends die de volksgezondheid in Nederland beïnvloeden. De VTV heeft een
vaste plaats in de nationale beleidscyclus voor de publieke gezondheid en wordt iedere vier
jaar uitgebracht door het RIVM. Het RIVM beschouwt alle beleidsmakers van het ministerie
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van VWS als belangrijkste beoogde gebruikers, maar RIVM-onderzoekers ervaren dat verre
van alle beleidsmakers bekend zijn met de VTV en dat de groep gebruikers nog flink kan
worden uitgebreid.
Om te onderzoeken hoe de VTV-bijdrage aan het nationale gezondheidsbeleid kan worden
versterkt, hebben we het ontwikkelingsproces van de VTV 2010 geanalyseerd. Daarbij
hebben we net als in de twee voorgaande casestudies Contribution Mapping toegepast. Om
data te verzamelen omvatte deze studie de analyse van documenten uit het VTV-2010 proces
en semigestructureerde diepte-interviews met belangrijke spelers, die vanuit RIVM en het
Ministerie van VWS betrokken waren bij de VTV 2010. Interviewers, die onafhankelijk waren
van RIVM en het Ministerie van VWS, voerden de interviews uit met de RIVM-onderzoekers
enhunmanagersopdrieniveaus(n=10)enmetdeVWSbeleidsmakersenhunmanagers
opdrieniveaus(n=10).Vervolgensidentificeerdenwebelangrijkegebiedenvooralignment
efforts met behulp van een constante vergelijkende analysemethode.
De VTV wordt in de literatuur beschouwd als voorbeeld van succesvol ‘boundary work’
(grenswerk). Het VTV-2010-proces bevatte inderdaad verschillende vaste activiteiten gericht
op de afstemming tussen onderzoekers en beleidsmakers, zoals informele vergaderingen.
Toch hebben we drie onderwerpen geïdentificeerd, die gemakkelijk over het hoofd worden
gezien in kennisontwikkeling, maar wel een aanknopingspunt bieden voor een betere
bijdrage aan beleid. Het eerste onderwerp is aandacht voor de verschillende en voortdurend
veranderende actorscenario’s; het tweede onderwerp is aandacht voor effectieve verticale
afstemming binnen de betrokken organisaties; en het derde onderwerp is aandacht voor
zorgvuldige timing van commentaarrondes voor concept-kennisproducten om zo ‘early
adopters’ van kennisproducten te creëren. We hebben geconstateerd dat voor het vergroten
van de bijdrage aan beleid van een bestaand volksgezondheidsrapport als de VTV, het
onvoldoende is om van potentiële nieuwe gebruikers aandacht te vragen voor het bestaande
product. Het kennisproduct moet namelijk ook afgestemd worden op de behoefte van de
nieuwe gebruikers en moet worden opgenomen in het actorscenario van deze nieuwe, voor
de onderzoekers minder bekende gebruikers. Om bestaande gebruikers ook binnenboord te
houden, moet de noodzaak voor het aanpassen van een bestaand kennisproduct echter wel
zorgvuldig worden overwogen. Dit vereist voortdurende alignment efforts in alle richtingen:
horizontaal en verticaal, extern en intern.
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Hoofdstuk 6. Research for Policy (R4P): ontwikkeling van een reflectietool voor
onderzoekers om kennisgebruik te verbeteren
In de drie vorige hoofdstukken hebben we uitgebreid drie complexe onderzoeksprojecten, die
waren uitgevoerd in opdracht van het Ministerie van VWS, geëvalueerd om te onderzoeken
hoe de afstemming in een onderzoeksproces bereikt wordt en om mogelijkheden te
ontdekken voor het verbeteren van de kennisbijdrage aan het gezondheidsbeleid. We
constateerden dat afstemming tussen onderzoekers en beleidsmakers tijdens de productie
van kennis weliswaar essentieel, maar ook moeilijk vast en vol te houden is. In dit hoofdstuk
beschrijven we hoe we de bevindingen van de drie casestudies integreerden in een praktische
tool voor onderzoekers om hun bijdrage aan evidence-informed beleid te versterken.
Door middel van een cross-case analyse van de drie casestudies identificeerden we de
volgende acht belangrijke gebieden voor afstemming:
1. het doel van het project,
2. de taken en verantwoordelijkheden van de betrokkenen,
3. de kwaliteit van de onderzoeksmethode,
4. de overlegstructuur van het project,
5. de verticale afstemming binnen organisaties,
6. de organisatorische omgeving van het project,
7. de relevantie en de timing van kennisproducten,
8. de presentatie van de onderzoeksresultaten.
Aangezien we hebben vastgesteld dat afstemming tussen onderzoek en beleid
voortdurende inspanningen (alignment efforts) vereist met daarbij inzicht in het proces
van het onderzoeksproject, hebben we een instrument ontwikkeld om onderzoekers te
ondersteunen in hun alignment efforts. Ons uitgangspunt daarbij was dat we onderzoekers
willen aanmoedigen om te reflecteren op het proces om zo bewust te worden van een
eventuele noodzaak tot afstemmen.
Rekening houdend met de acht geïdentificeerde afstemmingsgebieden hebben we in een
iteratief proces een hulpmiddel (tool) met praktische reflectievragen voor de onderzoeker
ontwikkeld. Deze Research for Policy tool (R4P-tool) werd getest door de RIVM projectleiders
van drie nieuwe onderzoeksprojecten in 2015. Zij vonden de R4P-tool nuttig als checklist voor
afstemming in een onderzoeksproject. Op basis van hun feedback werden verhelderende
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voorbeelden uit de casestudies toegevoegd aan de reflectievragen. De projectleiders stelden
voor om de R4P-tool niet alleen toegankelijk te maken voor onderzoekers maar ook voor
beleidsmakers. We hebben het format van de R4P-tool verder aangepast aan de behoefte
van de gebruikers door aanklikbare links toe te voegen. De R4P-tool biedt zo een praktische
richtlijn voor de benodigde afstemming en hulp bij reflectie op het proces, wat onderzoekers
ondersteunt bij het afstemmen met beleidsmakers en bij het omgevingsbewust handelen.
Hoofdstuk 7. Discussie en conclusie
In dit hoofdstuk wordt de studie als geheel besproken, inclusief een reflectie op de
onderzoeksbevindingen in relatie tot de onderzoeksvragen en een reflectie op de toegepaste
methoden. Tot slot worden mogelijke invalshoeken voor verder onderzoek benoemd en
wordt het hoofdstuk afgerond met de conclusie van deze studie.
De onderzoeksbevindingen van de drie casestudies (hoofdstukken 3, 4 en 5) en de cross-
case analyse van de drie casestudies (hoofdstuk 6) leverden een antwoord op de eerste
onderzoeksvraag:
Welke afstemmingsgebieden zijn belangrijk om de bijdragen aan gezondheidsbeleid te
versterken van projecten uitgevoerd door NPHIs in opdracht van de overheid?
Uit de casestudies hebben we acht afstemmingsgebieden geïdentificeerd waarvoor
specifieke aandacht nodig is om te voorkomen dat niet-afgestemde situaties tijdens het
onderzoek ontstaan (hoofdstuk 6). Deze gebieden zijn in overeenstemming met kritische
factoren voor kennisgebruik zoals genoemd in de wetenschappelijke literatuur. Een andere
belangrijke bevinding is echter dat het bereiken van afstemming in de praktijk erg moeilijk
is. Afstemming vereist voortdurend aandacht voor details, bewustzijn van kritische factoren,
kennis over de belangen en zorgen van de andere stakeholders en politieke sensitiviteit. Dit
zorgt ervoor dat alignment efforts veel meer tijd kosten dan voorzien en dat onderzoekers
naast interesse in wetenschappelijke problemen ook interesse in het proces nodig hebben
om te kunnen volharden in alignment efforts.
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De tweede onderzoeksvraag was:
Op basis van de empirische bevindingen van deze studie, wat is een praktische aanpak om
kennisbijdragen van NPHI’s aan evidence-informed gezondheidsbeleid op nationaal niveau
te verbeteren?
In de case-studies zagen we dat voor goede afstemming voortdurende reflectie op het
proces nodig is. We ontwikkelden de reflectie-tool R4P om onze bevindingen op een
praktische manier beschikbaar te maken voor onderzoekers en hen ondersteuning te
bieden bij het bepalen van het benodigde type en de benodigde omvang van alignment
efforts (hoofdstuk 6). Toch willen we benadrukken dat de R4P-tool alleen effectief gebruikt
kan worden in een organisatorische omgeving die aan bepaalde voorwaarden voldoet.
Aangezien continue aandacht voor het proces lastig is vol te houden, hebben onderzoekers
ondersteuning nodig bij reflectie en alignment efforts. De belangrijkste randvoorwaarden
voor voldoende afstemming zijn (1) een faciliterende organisatie, (2) afstemming als een
tweerichtingsproces en (3) een juiste balans in de wetenschappelijke onafhankelijkheid en
het afstemmen met de behoeften van de opdrachtgever.
Een faciliterende organisatie van een kennisinstituut beloont niet alleen wetenschappelijke
prestaties maar ook de alignment efforts om het proces goed te laten verlopen, zodat
onderzoekers gemotiveerd worden om tijd en energie te besteden aan dit vaak onzichtbare
deel van hun baan. Verder heeft afstemming baat bij enige flexibiliteit in de interacties van
onderzoekers met beleidsmakers, hetgeen betekent dat er voldoende manoeuvreerruimte
op alle organisatorische niveaus moet zijn voor alignment efforts. Verticale afstemming
zou een belangrijk aandachtspunt voor kennisinstituten moeten zijn, aangezien we zagen
dat te weinig verticale afstemming duidelijk de kennisbijdrage belemmert. Ook zouden
zowel de beleids-makende organisaties als NPHIs kunnen overwegen om een vorm van
afstemmingsborging te implementeren, bijvoorbeeld door speciale afstemmingsexperts aan
te stellen, die afstemmingsstrategieën ontwikkelen, die hun collega’s ondersteunen om die
strategieën te gebruiken en die de organisatie alert houden voor afstemmingsvraagstukken.
Om afstemming te bereiken is een tweerichtingsproces nodig. Voor een optimaal resultaat
moeten zowel het NPHI als de opdrachtgever tijd en energie te steken in het proces en zich
committeren om te investeren in alignment efforts. We zagen dat bij een kennisproduct dat
is ingebed in een formele procedure, zoals bij de VTV, de inspanningen om het proces goed te
laten verlopen toenemen bij zowel het NPHI als de opdrachtgevende overheidsorganisatie.
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Samenvatting | 199
S
Toch zijn alignment efforts op verschillende organisatorische niveaus in twee richtingen
ook nodig voor de kleine projecten van minder strategisch belang, aangezien alle projecten
bijdragen aan de relatie tussen de NPHI en de opdrachtgever op lange termijn.
Afstemming met de behoefte van de opdrachtgever om tot een optimale bijdrage aan beleid
te komen, kan in strijd lijken met de wetenschappelijke onafhankelijkheid van het NPHI.
Tegenwoordig wordt het gezag van overheidsorganisaties niet zonder meer geaccepteerd
en stellen mensen de NPHI adviezen, bijvoorbeeld over vaccinatie, openlijk ter discussie.
De uitdaging voor onderzoekers is om af te stemmen met beleidsmakers en afgestemd te
blijven, terwijl ze tegelijk hun onafhankelijke wetenschappelijke rol vasthouden en daarbij
geen schijnbare belangenverstrengeling creëren. NPHIs moeten daarom hun medewerkers
ondersteunen bij het ontwikkelen van de specifieke vaardigheden die nodig zijn voor het
werken in de nexus van wetenschap en gezondheidsbeleid.
In deze studie hebben we een kwalitatieve casestudie benadering gebruikt die een
diepgaand onderzoek van de projecten mogelijk maakte. Voor de data analyse bood
Contribution Mapping een functioneel driefase-model om de alignment efforts te
ontrafelen. Tijdens de ontwikkeling van de R4P-tool werd duidelijk dat de reflectievragen
voor de drie verschillende fasen elkaar overlappen en grotendeels identiek moesten zijn. De
uiteindelijke R4P-tool is daarom ingedeeld op proces-onderwerpen in plaats van op de drie
fasen van het onderzoeksproces. We beschouwen Contribution Mapping een waardevolle
methode voor het evalueren van het alignment-systeem van een kennisinstituut, omdat het
de institutionele patronen blootlegt waarvoor actie vereist is. Aangezien de methode veel
tijd en moeite vergt, ligt toepassing voor de evaluatie van een klein project minder voor de
hand.
Mogelijke invalshoeken voor verder onderzoek zijn de verdere ontwikkeling van de R4P-tool,
Europese verschillen in afstemming en alignment efforts en de implicaties van activistisch
scepticisme ten opzichte van wetenschap. De R4P-tool moet gevalideerd worden op
effectiviteit (daadwerkelijke meer afstemming) en kan uitgebreid worden naar andere
onderzoeksdomeinen. Voor werken in Europees verband en in internationale netwerken
is het nuttig om te onderzoeken of culturele verschillen tussen landen invloed hebben
op afstemming en alignment efforts. Deze inzichten kunnen worden gebruikt om ook op
internationaal niveau de bijdrage van wetenschappelijke kennis aan gezondheidsbeleid te
verbeteren.
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200 | Samenvatting
Op basis van onze studie stellen we dat kennisinstituten moeten erkennen dat het
bereiken van afstemming veel meer inspanning, tijd en middelen nodig heeft dan vaak
wordt verondersteld. Het uitvoeren van onderzoek bij een NPHI en het genereren van
kennisproducten in opdracht van overheidsorganisaties ten behoeve van evidence-
informed gezondheidsbeleid vraagt de nodige behendigheid om de juiste balans te houden
tussen afstemming en onafhankelijkheid. Door het instituut te organiseren op een wijze
die dit balanceren vergemakkelijkt en ondersteunt, kan het NPHI zijn bijdragen aan het
gezondheidsbeleid optimaliseren.
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Dankwoord | 201
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Dankwoord
Mijn promotietraject was een lang en leerzaam proces, waarin ik veel hulp, morele steun en
vertrouwen van de mensen om mij heen heb ondervonden. Daar ben ik bijzonder dankbaar
voor!
Allereerst wil ik mijn promotores Hans van Oers en Jantine Schuit bedanken. Zij hebben
steeds ruim tijd voor mijn begeleiding vrij gemaakt. In onze IKU-overleggen was de sfeer
bijzonder goed en hebben we ook veel gelachen.
Hans, jij hebt mij steeds weer teruggebracht naar de kern van het probleem en mij geholpen
door de bomen het bos te blijven zien. Je vertrouwen in mij heeft mij enorm geholpen in de
afgelopen jaren.
Jantine, jouw visie en inbreng over de context van ons werk zijn heel waardevol voor mij
geweest. Je verlaat spijtig genoeg het RIVM, tegelijk is het ook mooi dat je de decaan bent
geworden van de faculteit waar ik mijn proefschrift mag verdedigen.
In de dagelijkse praktijk werd ik in mijn onderzoek gesteund door mijn co-promotor en
leidinggevende Susan Janssen. Susan, naast je inhoudelijke bijdrage aan mijn proefschrift,
heb je mij steeds de ruimte en gelegenheid gegeven om te werken aan dit onderzoek en mij
aangemoedigd vol te houden. Daar wil ik je heel graag voor bedanken!
Zonder de directe medewerking van een aantal mensen had ik het onderzoek niet kunnen
uitvoeren. Jolanda Keijsers was als meedenker van het eerste uur betrokken bij de opzet
van de studie en twee artikelen. Joyce de Goede heeft mij op weg geholpen na haar eigen
promotietraject en was steeds beschikbaar voor advies. Lisanne Marks heeft aanvankelijk
als student en later als collega meegewerkt aan de studie naar de Zorgbalans 2010 en
de ontwikkeling van de R4P-tool. Tijdens haar studie is Lisanne vanuit iBMG, Erasmus
Universiteit begeleid door Roland Bal, die ook een bijdrage heeft geleverd aan het overzicht
van theoretische benaderingen van kennis voor beleid. Maarten Kok heeft mij geïnspireerd
met zijn theoretische beschouwingen en een aandeel geleverd in de studie naar de VTV
2010. Peter Schouten was als student betrokken in het eerste onderdeel van de studie naar
VTV 2010 bij de start van het onderzoek. Jolanda, Joyce, Lisanne, Roland, Maarten en Peter,
bedankt voor jullie waardevolle bijdrage aan mijn onderzoek.
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202 | Dankwoord
De leden van de leescommissie bedank ik van harte voor alle tijd en moeite die zij hebben
besteed aan het beoordelen van mijn proefschrift. Geachte leden van de leescommissie, ik
stel het bijzonder op prijs dat u allen mij zo verder heeft willen helpen.
Als senior RIVM onderzoeker kreeg ik de mooie kans om alsnog te promoveren. Ik bedank
mijn werkgever RIVM, vertegenwoordigd in de personen Annemieke de Vries, Xandra
Gravestein, Henriëtte Treurniet, Rogier Bos, Annemiek van Bolhuis en André van der Zande,
dat ik hiertoe in de gelegenheid ben gesteld.
Mijn naaste collega’s zijn altijd belangrijk voor mij, maar hun onmisbaarheid voelde ik
zeker tijdens mijn promotietraject. Dank jullie wel voor de feedback die specifiek op mijn
proefschrift was gericht, maar ook voor alle collegialiteit, steun en gezelligheid die jullie mij
op het werk schenken! Gelukkig houdt onze samenwerking ook na de afronding van mijn
proefschrift niet op.
Terwijl ik mijn promotieonderzoek verrichtte, ging het leven natuurlijk gewoon door en
bracht naast fijne gebeurtenissen ook turbulenties met moeilijke momenten. Het was voor
mij belangrijk dat ik op die momenten zo veel mensen om mij heen had die mij op een of
andere manier hebben gesteund en mij aanmoedigden de draad van het proefschrift vast
te houden. Ik bedank mijn vriendinnen en vrienden voor hun interesse, begrip en voor alle
vrolijke ontspanning, tijdens gezellige etentjes, de repetities van het WP-koor, de NoWaBi-
wandelingen, de koffie na gedane fitness-inspanning, de maandelijkse Vrijmibo-gesprekken
en de uitjes met de Cult-club.
Mijn familie van Hegger-, Dämmler- en Bakker-kant vormt een liefdevolle kring van
dierbare mensen om mij heen. Ik bedank mijn familieleden allemaal voor de interesse in
de vorderingen van mijn ‘boek’, de aanmoedigingen en het vertrouwen in de goede afloop
ondanks mijn lange doorlooptijd om dit af te ronden.
Een speciaal woordje richt ik tot mijn moeder. Mama, jij hebt mij met papa altijd door dik en
dun gesteund en jullie hebben altijd onvoorwaardelijk van mij gehouden, daarvoor hoefde
ik gelukkig niet te promoveren. Ik hoop nog heel lang samen met jou dingen te kunnen
ondernemen!
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Dankwoord | 203
D
Mijn kinderen hebben mij steeds geïnspireerd om door te zetten, zoals zij dat tegelijkertijd
ook deden in hun eigen studies. Matthijs, Thomas en Esther, in de jaren dat dit proefschrift
tot stand kwam hebben jullie je ontwikkeld tot prachtige, liefdevolle volwassenen met een
eigen leven en lieve, leuke partners. Ik vind het fijn dat Sephora, Anouk en Richard ook een
onderdeel van mijn leven zijn geworden.
Tot slot bedank ik mijn levensmaatje. Lieve Herman, mijn promotietraject en alles
wat verder in die periode gebeurd is, hebben we samen goed doorstaan. Je hebt me
steeds aangemoedigd bij het schrijven van mijn proefschrift en mij geholpen met jouw
vanzelfsprekende zorgzaamheid, zoals het brengen van thee naar zolder en het eten klaar
hebben op een tijdstip dat handig was voor mijn schrijf-flow. Nu mijn proefschrift is afgerond,
verheug ik me op de zee aan vrije tijd samen.
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204 | About the author
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About the author | 205
A
About the author
Ingrid Hegger was born on November 11th, 1960 in The Hague, the Netherlands. She
studied Pharmacy at the University of Leiden, the Netherlands from 1979 until 1986 and
obtained the professional title of pharmacist at the University of Utrecht, the Netherlands
in November 1987.
Since February 1988, she works at the National Institute for Public Health and the
Environment in Bilthoven, the Netherlands. She became an expert in the quality of biological
and biotechnological medicinal products and in the European regulation of medicinal
products. In her professional life, she has been involved in many national and international
activities related to the quality of biological medicinal products: the EU control authority
batch release of immunological medicinal products and plasma derived products; the
scientific assessment of biological medicinal products for marketing authorization and the
standardization of vaccines in the European Pharmacopoeia.
From 1999 onwards, the focus in her work shifted from the product quality of biologicals
towards “close-to-policy” projects in the field of medicinal products, pharmaceutical care
and the regulatory system for medicinal products. She has been involved in projects on
the regulation of medicinal products, investigational medicinal products for clinical trials,
advanced therapies, pharmaco-economics, orphan diseases, the influence of internet on
medicines use and the organization of pharmaceutical care. Currently, she is working on
personalized medicine, new technologies and the Dutch care system.
In 2011, she started as principal researcher in the RIVM research project “Improving
knowledge utilization”, granted by the RIVM strategic research programme. The study
conducted in this project is presented in this thesis.
Ingrid is married to Herman Bakker and together, they have three, now grown-up, children,
Matthijs, Thomas and Esther.
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206 | List of Publications (2011-2017)
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List of Publications (2011-2017) | 207
L
List of Publications
(2011-2017)
Publishedjournalarticles(2011-2017)
Hegger I, Marks LK, Janssen SWJ, Schuit AJ, Keijsers JFEM, van Oers HAM. Research for Policy
(R4P): a reflection tool for researchers to enhance contributions to policymaking. Implement
Sci. 2016; 11(133)
Hegger I, Kok MO, Janssen SWJ, Schuit AJ, van Oers HAM. Contributions of knowledge
products to health policy: a case study on the Public Health Status and Forecasts Report
2010. Eur JPublic Health. 2016; 26(6): 922-927.
Hegger I, Marks LK, Janssen SWJ, Schuit AJ, van Oers HAM. Enhancing the contribution of
research to health care policy-making: a case study of the Dutch Health Care Performance
Report. J Health Serv Res Policy. 2016; 21(1): 29-35.
Hegger I, Janssen SWJ, Keijsers JFEM, Schuit AJ, van Oers, HAM. Analyzing the contributions
of a government-commissioned research project: a case study. Health Res Policy Syst. 2014;
12(1): 8.
Jongen PM, van den Bogert CA, van de Laar CW, Notenboom K, Hille ET, Hegger I. Risk
indicator taxonomy for supervision of clinical trials on medicinal products. Curr Med Res
Opin. 2016; 32 (7):1269-1276.
Venhuis BJ, Keizers PHJ, Klausmann R, Hegger I. Operation resistance: A snapshot of falsified
antibiotics and biopharmaceutical injectables in Europe. Drug Test Anal. 2016; 8(3-4):398-
401.
Van Kerkhof LWM, van de Laar CWE, de Jong C, Weda M, Hegger I. Characterization of apps
and other e-tools for medication use: insights into possible benefits and risks. JMIR MHealth
UHealth. 2016 ; 4(2):e34
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208 | List of Publications (2011-2017)
Van Berkel JJ, Lambooij MS, Hegger I. Empowerment of patients in online discussions about
medicine use. BMC Med Inform Decis Mak. 2015; 15:24
Submitted journal articles
Hegger I, Marks L, Bal RA, van Oers HAM. The complex relationship between research and
health policy: a comprehensive overview of theoretical approaches.
Moltó-Puigmartí C, Vonk RAA, van Ommeren GL, Hegger I. A logic model for product- and
patient-focused pharmaceutical care.
RIVMreports(2011-2017)
Hegger I, Moltó-Puigmartí C. Registratie op werkingsmechanisme: Een verkenning naar de
mogelijkheden om geneesmiddelen te registreren op werkingsmechanisme. RIVM report
2016-0214. Bilthoven: RIVM; 2016.
Van Berkel J, Lambooij M, Hegger I. Luisteren naar de digitale patiënt: verkennende analyse
van gesprekken op social media over medicatie en ziekte. RIVM report 2015-0160. Bilthoven:
RIVM; 2015.
Woutersen M, Tiesjema G, Jeurissen S, de Bruijn A, Herremans J, Hegger I. Producten op
de grensvlakken Warenwet-Wet op de medische hulpmiddelen-Biocideverordening. RIVM
report 2015-0184. Bilthoven: RIVM; 2015.
Van Kerkhof L, van de Laar K, Schooneveldt B, Hegger I. e-Medication met behulp van apps.
RIVM report 2015-015. Bilthoven: RIVM; 2015.
Vonk RAA, van de Laar, CWE, Hegger I, Ezendam J, Janssen SWJ, Hoebert JM. Legal barriers
for the use of alternatives to animal testing: do current EU regulations and guidelines for
regulatoryacceptanceofmedicinalproductsposelegalbarriers?RIVMreport2015-0084.
Bilthoven: RIVM; 2015.
Hoebert JM, Vonk RAA, van de Laar CWE, Hegger I, Weda M, Janssen SWJ. Minds Open
Sustainability of the Euroepan regulatory system for medicinal products. RIVM report 2014-
0033. Bilthoven: RIVM; 2014.
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List of Publications (2011-2017) | 209
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Hegger I, Janssen SWJ. Betrouwbare geneesmiddeleninformatie beter toegankelijk voor de
gebruiker! Een gezamenlijke inspanning van CBG, Lareb, RIVM en Zorginstituut Nederland.
RIVM letterreport 132054001. Bilthoven: RIVM; 2014.
Hegger I, Akkermans A, Notenboom K, de Vries B. Efficiency en uitkomst van onaangekondigde
GMP-inspecties bij farmaceutische bedrijven. RIVM report 360006002. Bilthoven: RIVM;
2012.
Notenboom K, Molema-Buursma AR, Hegger I. Contract Research Organisaties in Nederland:
inventarisatie en kwaliteitsniveau. RIVM report 370005001. Bilthoven: RIVM; 2011.
Conferencecontributions(2011-2017)
Hegger I, Marks LK, Janssen SWJ, Schuit AJ, Keijsers JFEM, van Oers HAM. Research for Policy
(R4P): a reflection tool for researchers based on the evaluation of knowledge contributions
to policy-making. Presentation at EES Conference 29 September 2016, Maastricht, the
Netherlands.
Hegger I, Marks LK, Janssen SWJ, Schuit AJ, Keijsers JFEM, van Oers HAM. Research for
Policy (R4P): a reflection tool for researchers to enhance contributions to policymaking.
Presentation at FUSE conference 27 April 2016, NewCastle, UK.
HeggerI,VonkR,vandeLaarK.Thecommunitypharmacist:unknown,unloved,unwanted?
Research project on System Assessment Development for pharmaceutical patient care and
the pharmacist’s role in integrated primary care. Presentation at policy debate session,
European Forum for Primary Care Conference, 30 August -1 September, Amsterdam, the
Netherlands.
Van Berkel JJ, Lambooij MS, Hegger I. Empowerment of patients in online discussions
about medicine use. Presentation at International Conference on Health Informatics and
Technology, 27-29 July 2015, Valencia, Spain.
Van Kerkhof L, de Jong C, van de Laar K, Hegger I. Characterization of apps and other e-tools
for medication use. Presentation at International Conference on Health Informatics and
Technology, 27-29 July 2015, Valencia, Spain.
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210 | List of Publications (2011-2017)
Van Kerkhof L, de Jong C, van de Laar K, Weda M, Hegger I. eMedication met behulp van
apps – onderzoek naar kansen en risico’s. Presentation at Prisma Symposium, 19 mei 2015,
Amersfoort, the Netherlands.
Hegger I, Marks LK, Janssen SWJ, Schuit AJ, Keijsers JFEM, van Oers HAM. Kennisversneller:
beter laten doorwerken van kennis in beleid. Presentation at Nederlands Congres
Volksgezondheid 2014, 11 april 2014, Rotterdam, the Netherlands.
Hegger I, Kok MO, Janssen SWJ, Keijsers JFEM, Schuit AJ, van Oers HAM. Verbetering van
het gebruik van kennis voor beleid en toezicht. Poster-presentation at Nederlands Congres
Volksgezondheid 2012, 11-12 April 2012.
Research for Policy A
study on improving the contribution of scientific know
ledge to evidence-informed health policy
Ingrid Hegger
Research for PolicyA study on improving the contribution of
scientific knowledge to evidence-informed health policy
Ingrid Hegger
Evidence-informed health policy-making is generally considered as an important approach
for safeguarding public health: governments should take into account the best available
research evidence in health policy-making. Most countries have established a National
Public Health Institute to support their government in essential public health operations by
activities such as health protection, population health assessment and research to produce
evidence for policy-making. However, researchers experience that achieving contributions
to health policy-making appears to be more difficult than one would expect in view of the
institute’s mission. In the body of scientific literature on knowledge utilization, alignment
between researchers and policy-makers is recognized as an important key for enhancing
contributions of scientific knowledge to policy-making.
This thesis describes a study investigating how alignment is achieved and can be improved
in research projects conducted by a National Public Health Institute in commission of
governmental organizations.
Uitnodiging
voor het bijwonen van de openbare verdediging van mijn proefschrift
Research for PolicyA study on improving
the contribution of scientific knowledge to evidence-informed
health policy
op woensdag 6 september 2017 om 16:00 precies in de aula van de
Universiteit van Tilburg,Warandelaan 2 te Tilburg
Aansluitend bent u
van harte welkom opde receptie ter plaatse
Ingrid HeggerSoestdijkseweg Zuid 19
3732 HC De [email protected]
06-38464916
Paranimfen:Thomas Bakker
Esther [email protected]
De aula bevindt zich in het Cobbenhagengebouw,
te bereiken via het Koopmansgebouw. Bij de universiteit is voldoende
parkeergelegenheid. Station Tilburg Universiteit is op
10 minuten loopafstand.https://www.tilburguniversity.edu/nl/
contact/campus-map/