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Verkissen MN, Ezendam NPM, Fransen MP, Essink-Bot ML, Aarts MJ, Nicolaije KAH, Vos MC, Husson O. The role of health literacy in perceived information provision and satisfaction among women with ovarian tumors: A study from the population-based PROFILES registry. Patient Education and Counseling, 2014; in press.

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    Patient Education and Counseling xxx (2014) xxxxxx

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    PEC-4748; No. of Pages 8

    Contents lists available at ScienceDirect

    Patient Education

    jo ur n al h o mep ag e: w ww .e lseMarie-Louise Essink-Bot c, Mieke J. Aarts b, Kim A.H. Nicolaije a,b,M. Caroline Vos d, Olga Husson a,b

    aCoRPS Center of Research on Psychology in Somatic Diseases, Department of Medical and Clinical Psychology, Tilburg University, The Netherlandsb Eindhoven Cancer Registry, Comprehensive Cancer Center South (CCCS), Eindhoven Cancer Registry, The NetherlandscDepartment of Public Health, Academic Medical Center, University of Amsterdam, The NetherlandsdDepartment of Obstetrics and Gynecology, St. Elisabeth Hospital, Tilburg, The Netherlands

    1. Introduction

    The provision of appropriate information is one of the mostimportant aspects of the support for cancer survivors. Appropriateinformation provision, for example about the diagnosis, treatment,long-term effects, and care services, can result in informed decisionmaking, improved treatment adherence, lower levels of distress,and higher satisfaction with care and information received [16].Nevertheless, adequate information provision remains a challenge

    in the eld of cancer care. It has shown to be a common unmet needamong cancer survivors in all phases of their disease [7]. Effectiveinformation provision requires an individualized approach that istailored to the patients needs, competences, limitations, andpossible barriers to the use of health information [8]. Tailoredinformation may lead to improved outcomes, such as betteradjustment to treatment [9]. In general, patients want to beinformed about their disease and its implications, regardless ofwhether this information is positive or negative [10,11]. However,specic information needs may depend on many individualizedfactors, including education and health literacy [12,13].

    Health literacy (HL) entails peoples knowledge and compe-tences to access, understand, appraise, and apply health informa-tion [14]. After a cancer diagnosis, patients are often presented

    A R T I C L E I N F O

    Article history:

    Received 12 September 2013

    Received in revised form 18 February 2014

    Accepted 8 March 2014

    Keywords:

    Ovarian tumors

    Borderline ovarian tumors

    Cancer survivors

    Health literacy

    Information provision

    Information satisfaction

    A B S T R A C T

    Objective: To assess the association of subjective health literacy (HL) and education with perceived

    information provision and satisfaction.

    Methods: Women (N = 548) diagnosed with an ovarian or borderline ovarian tumor between 2000 and

    2010, registered in the Eindhoven Cancer Registry, received a questionnaire including subjective HL,

    educational level, perceived information provision, and satisfaction with the information received.

    Multiple linear and logistic regression analyses were performed, controlled for potential confounders.

    Results: Fifty percent of the women responded (N = 275). Thirteen percent had low and 41% had medium

    subjective HL. Women with low HL reported less perceived information provision about medical tests,

    and were less satised with the information received compared to women with high HL. Low educated

    women reported that they received more information about their disease compared to highly educated

    women.

    Conclusion: Low subjective HL among women with ovarian tumors is associated with less perceived

    information provision about medical tests and lower information satisfaction, whereas low education is

    associated with more perceived information provision about the disease.

    Practice implications: HL should not be overlooked as a contributing factor to patients perceived

    information provision and satisfaction. Health care providers may need training about recognizing low

    HL.

    2014 Elsevier Ireland Ltd. All rights reserved.

    * Corresponding author at: Comprehensive Cancer Center The Netherlands, 5600

    AE Eindhoven, The Netherlands. Tel.: +31 40 2971616; fax: +31 40 2971610.

    E-mail address: [email protected] (Nicole P.M. Ezendam).

    http://dx.doi.org/10.1016/j.pec.2014.03.008

    0738-3991/ 2014 Elsevier Ireland Ltd. All rights reserved.Health Literacy

    The role of health literacy in perceivedprovision and satisfaction among womA study from the population-based PRO

    Mariette N. Verkissen a,b, Nicole P.M. Ezendama,b,*Please cite this article in press as: Verkissen MN, et al. The role of heamong women with ovarian tumors: A study from the populatiodx.doi.org/10.1016/j.pec.2014.03.008formation with ovarian tumors:ILES registry

    irjam P. Fransen c,

    and Counseling

    vier . co m / loc ate /p ated u co ualth literacy in perceived information provision and satisfactionn-based PROFILES registry. Patient Educ Couns (2014), http://

  • with complex medical information regarding their disease andtreatment [15,16]. Patients with low HL are at high risk of not beingable to process the information they are provided. This puts themat risk for various negative outcomes, such as difculty under-standing the diagnosis and treatment recommendations, pooreradherence to medical advice, medication errors resulting frominability to read labels, and increased hospitalizations [1719]. HLcan be assessed using objective and subjective measures. ObjectiveHL measures assess the individuals actual skills (e.g. reading andcalculating), whereas subjective HL measures evaluate theindividuals perceived skills (e.g. asking if he or she has difcultyunderstanding health information). Education is often thought ofas a marker for HL. However, although HL and education arerelated to each other [20], they need to be understood as distinctconcepts [21,22].

    Despite the increased recognition of the importance of bothinformation provision and HL in cancer care, research on the role ofHL in information provision to cancer patients is limited. Previousstudies have examined the relation between breast cancerpatients HL and information-processing styles and preferences[23], breast cancer patients HL levels compared to the level ofwritten patient educational materials provided to them [24], and

    ask few questions during consults [28,29], we hypothesized thatlower HL would be associated with less perceived informationprovision among women with ovarian tumors. In the limited timethat physicians have with their patients, they may not be able totailor the information according to their needs. We thereforehypothesized that lower HL would be associated with lesssatisfaction with the information received. Finally, based onprevious research indicating that patients with lower educationallevels generally feel less condent and are more likely to be passivein interactions with physicians [30], we hypothesized that lowereducation would also be associated with less perceived informa-tion provision and less satisfaction with the information received.

    2. Methods

    2.1. Setting and participants

    This study is part of a population-based survey among womenwith ovarian cancer and BOT registered within the EindhovenCancer Registry (ECR). The ECR collects data of all individualsnewly diagnosed with cancer in the southern part of theNetherlands [31]. All women diagnosed with ovarian cancer or

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    PEC-4748; No. of Pages 8the relation between cancer patients HL and self-reportedinformation needs [22,25]. To our knowledge, however, no studieshave focused on the relation of cancer survivors HL with perceivedinformation provision and satisfaction with the informationreceived.

    The present paper describes an explanatory study focusing onthe additional effect of HL over education on information provisionin a population-based sample of Dutch women with ovarian cancerand borderline (low malignant potential) ovarian tumors (BOT).Cancer of the ovary is one of the most common gynecologicmalignancies, whereas BOT are relatively uncommon. In theNetherlands, about 1300 cases of ovarian cancer and 150200cases of BOT are diagnosed annually [26,27].

    The main purpose of this study was to investigate theassociation between HL and perceived level of informationprovision and information satisfaction, controlling for educationallevel. In order to distinguish between the potentially differenteffects of HL and education, we also evaluated the associationbetween educational level and perceived level of informationprovision and satisfaction. Given that patients with inadequate HLtend to be passive during physicianpatient communication and

    1442 women were dia gnosed and registered witovarian ca ncer (114 7) or bord erli ne ovarian tumo(BOT) (2 95) between Ja nuary 1

    st 2000 and July

    2010 in 6 hospitals in the Eindhoven Cancer Registry region

    719 patients were still alive on September 15th

    20(454 ov arian ca ncer; 265 BOT)

    Their gy necologists receiv ed an invitation letter tpermit st udy par ticipation

    Addresses of 351 ovarian cancer and 202 BOTpatients were ch ecked for correctn ess

    A questio nna ire was sent to the remaining ovaria

    cancer (348) and BOT (2 00) patients

    Patients included in the st udy: 191 (55%) ovaria

    cancer and 84 (42%) BOT

    Fig. 1. Flowchart of the Please cite this article in press as: Verkissen MN, et al. The role of heamong women with ovarian tumors: A study from the populatiodx.doi.org/10.1016/j.pec.2014.03.008BOT between January 1, 2000 and July 1, 2010 as registered withinthe ECR were eligible for participation (N = 1442; Fig. 1). Deceasedpatients were excluded by linking the ECR with the Central Bureaufor Genealogy. Ethical approval for the study was obtained fromthe Medical Ethics Committee of St. Elisabeth Hospital, Tilburg, theNetherlands (no. 2011.129).

    2.2. Data collection

    Data collection took place in 2012. Along with a paperquestionnaire, patients received a letter from their specialistexplaining the survey and an informed consent form. Non-respondents were sent a reminder letter and questionnaire within2 months. Patients were asked to send the informed consent formand questionnaire back to the researchers in a pre-stampedenvelope.

    The PROFILES (Patient Reported Outcomes Following Initialtreatment and Long term Evaluation of Survivorship) registry wasused to organize the data collection. PROFILES is an infrastructurefor the study of the physical and psychosocial impact of cancer andits treatment from a dynamic, growing population-based cohort of

    723 patients deceased (6 93 ovarian

    cancer; 30 BOT )

    1 hospital declin ed (N=12 7) (74 ovarian ca ncer; 53 BOT)

    Excluded: 29 ovarian ca ncer; 10 BOT (d eceased, hospitalized,

    nursing home)

    Addresses unkn own: 3 ov arian cancer; 2 BOT

    Non-responders: 157 (45 %) ovarian

    cancer; 116 (48%) BO T

    ta collection process.alth literacy in perceived information provision and satisfactionn-based PROFILES registry. Patient Educ Couns (2014), http://

  • M.N. Verkissen et al. / Patient Education and Counseling xxx (2014) xxxxxx 3

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    PEC-4748; No. of Pages 8both short and long-term cancer survivors [32]. PROFILES containsa large web-based component and is linked directly to clinical datafrom the ECR. Data from the PROFILES registry are available fornon-commercial scientic research, subject to study question,privacy and condentiality restrictions, and registration (http://www.prolesregistry.nl/).

    2.3. Measures

    2.3.1. Clinical and socio-demographic characteristics

    Clinical and patient information was obtained from the ECR (i.e.,date of birth, date of diagnosis, tumor grade, and primarytreatment). Socio-economic status (SES) was determined at theneighborhood level using postal codes, combining mean house-hold income and mean value of housing, as provided by StatisticsNetherlands [33]. The questionnaire contained questions oneducational level, employment status, and marital status.

    2.3.2. Subjective health literacy

    A Dutch adaptation of Chews three-item Set of Brief ScreeningQuestions (SBSQ) was used to evaluate subjective HL [34]. TheAmerican version of the SBSQ has been previously validatedagainst widely used measures of health literacy (REALM and S-TOFHLA) as the reference standard [35,36] across a variety ofsettings [3739]. Previous research has suggested that a scalecombining the three items is no more effective in identifyingindividuals with inadequate HL than one single item [3537,40]. Ithas also been demonstrated that the item How condent are youlling out medical forms by yourself? (very, quite, some-what, a little and not at all) is more effective in predictinginadequate HL than the other two items [37,40]. Therefore, thissingle item was used in the analyses.

    2.3.3. Perceived information provision and satisfaction

    To evaluate the perceived level of and satisfaction withinformation provision, the Dutch version of the EuropeanOrganization for Research and Treatment of Cancer (EORTC)QLQ-INFO25 questionnaire, an instrument to assess the infor-mation given to cancer patients, was used [41]. Patientsresponses to the EORTC QLQ-INFO25 were collated into foursubscales: (1) perceived receipt of information about the disease(four items regarding diagnosis, spread of disease, cause(s) ofdisease and whether the disease is under control); (2) medicaltests performed in relation to the disease (three items regardingpurpose, procedures and results of tests); (3) treatment (sixitems regarding medical treatment, benets, side-effects, effectson disease symptoms, social life and sexual activity); and (4)other care services (four items regarding additional help,rehabilitations options, managing illness at home, psychologicalsupport). The question format was as follows: During yourcurrent disease or treatment, how much information did youreceive on. . .?. Additionally, the questionnaire contained asingle item regarding patients satisfaction with informationreceived (Were you satised with the amount of informationyou received?).

    The response options were not at all, a little, quite a bit,and very much. After linear transformation, all scales and itemsrange in scores from 0 to 100, with higher scores indicating betterperceived information provision or higher satisfaction [3].

    The EORTC QLQ-INFO25 has a good scale structure and has beeninternationally validated [41,42]. Internal consistency for all scalesand test-retest reliability have been reported to be good (a > 0.70and intraclass correlations > 0.70, respectively) [41]. Our datarevealed Cronbachs alphas of 0.80 (disease), 0.90 (medical tests),0.88 (treatment), and 0.81 (other care services) for the foursubscales.Please cite this article in press as: Verkissen MN, et al. The role of heamong women with ovarian tumors: A study from the populatiodx.doi.org/10.1016/j.pec.2014.03.0082.4. Statistical analyses

    All statistical analyses were conducted using IBM SPSS Statisticsversion 19 (SPSS Inc., Chicago, IL, USA). p-Values of

  • 3.2. Subjective health literacy and educational level

    Thirteen percent of the women had low subjective HL; 41% hadmedium subjectiveHL.Fifteenpercenthada loweducational level;64%had a medium educational level (Table 2). HL and educational levelwere signicantly related to each other (p < 0.001). Of women withhigh HL (N = 119), 33% had a high educational level as well, and of allwomen with low HL (N = 33), 49% had a low educational level as well.

    3.3. Educational level, subjective health literacy, and perceived

    information provision

    On average, low educated women reported a lower perceivedlevel of information provision about medical tests and treatmentcompared to highly educated women, and women with lowsubjective HL reported a lower perceived level of informationprovision about disease, medical tests, and treatment compared towomen with high HL (Table 2).

    Table 1Socio-demographic and clinical characteristics of questionnaire respondents and

    non-respondents.

    Respondents Non-respondents p-Value

    N = 275 N = 282

    N (%) N (%)

    Age at time of survey (mean, SD) 62.8 (12.4) 60.9 (14.3) 0.10

    Years since diagnosis (mean, SD) 6.3 (3.1) 6.4 (3.1) 0.55

    Tumor type

    Ovarian tumor 191 (70%) 163 (58%)

  • provision related to medical tests. We found similar trendsregarding perceived information provision about disease andtreatment, but these trends were not statistically signicant.Women with low HL were also less likely to be satised with theinformation received compared to women with high HL. Thesendings are in line with our hypotheses, and with previousresearch showing that patients with low HL were more likely toreport worse patientphysician communication in the domains ofinformation provision about disease and care processes (e.g.medical tests) [48]. Besides problems with reading, writing andnumeracy, patients with low HL may have difculty processingoral communication, assimilating new information, comprehend-ing health vocabulary and asking questions during visits with theirhealth care professional [48,49]. If health care providers lack thetime or skills necessary to help patients with low HL fullyunderstand their condition, the information provided to patientswith low HL may not correspond with their information needs.This may lead to patient dissatisfaction. Moreover, patients tend toforget a signicant amount of the information they received whenthis information is complex and emotionally charged [50], whichmay be particularly true for patients with low HL because of their

    0

    5

    10

    15

    20

    25

    Informationdisease

    Informationmedical tests

    Information treatme nt

    Information othercare services

    Perc

    enta

    ge

    Health literacy (step 3)

    Educati onal lev el (st ep 2)

    Confo unders (st ep 1)

    *

    *

    Fig. 2. Explained variance (R2 (%)) of the EORTC QLQ-INFO25 perceived informationprovision subscales by the confounders tumor type, years since diagnosis, age at

    M.N. Verkissen et al. / Patient Education and Counseling xxx (2014) xxxxxx 5

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    PEC-4748; No. of Pages 8Hierarchical multiple logistic regressions revealed no signi-cant association between educational level and informationsatisfaction. Compared to patients with high subjective HL, womenwith low HL were signicantly less likely to be satised with theinformation they received (OR = 0.2 (0.1; 0.6); Table 4).

    4. Discussion and conclusion

    4.1. Discussion

    In the present study, lower subjective HL was associated withless perceived information provision about medical tests and lowerinformation satisfaction. Contrary to our hypothesis, low educa-tional level was associated with more perceived informationprovision about the disease compared to high educational level. HLand educational level explained a relatively small amount of thevariability in perceived information provision and informationsatisfaction.

    time of survey, employment status and marital status (step 1); plus educational

    level (step 2); plus subjective health literacy (step 3). *p < 0.05.Compared to women with high subjective HL, women withmedium and low HL scored lower on perceived information

    Table 3Hierarchical multiple linear regression analyses evaluating the associations of education

    High

    educationaMedium education Low education Hi

    HL

    Information disease

    Model 2 (B, 95% CI) Ref 2.3 (10.0; 5.5) 12.4 (1.1; 23.6)*Model 3 (B, 95% CI) Ref 1.5 (9.3; 6.2) 15.5 (3.8; 27.2)* Re

    Information medical tests

    Model 2 (B, 95% CI) Ref 5.6 (14.5; 3.4) 0.9 (13.9; 12.1) Model 3 (B, 95% CI) Ref 4.3 (13.1; 4.6) 3.4 (10.0; 16.7) Re

    Information treatment

    Model 2 (B, 95% CI) Ref 3.6 (12.2; 4.9) 3.7 (8.6; 16.0) Model 3 (B, 95% CI) Ref 2.8 (11.3; 5.8) 7.0 (5.8; 19.7) Re

    Information other care services

    Model 2 (B, 95% CI) Ref 7.0 (1.1; 15.1) 8.8 (2.8; 20.5) Model 3 (B, 95% CI) Ref 7.0 (1.2; 15.1) 9.7 (2.5; 22.0) Re

    Note: Model 1 (not reported) includes tumor type, years since diagnosis, age at time of sur

    education level; Model 3 includes all of Model 2 as well as subjective health literacya Educational level: high = university or higher education; medium = secondary educb HL = subjective health literacy: high = being very condent lling out medical forms;

    little or not at all condent lling out medical forms* p < 0.05.

    Please cite this article in press as: Verkissen MN, et al. The role of heamong women with ovarian tumors: A study from the populatiodx.doi.org/10.1016/j.pec.2014.03.008poor ability to recall information provided during medicalconsultations [51].

    Contrary to our hypothesis that patients with a lowereducational level would indicate that they received less informa-tion, low educated women reported that they received moreinformation about their disease compared to highly educatedwomen. Previous studies found that having a lower level ofeducation was associated with less perceived information provi-sion about medical tests and treatment [6,45,47] and with atendency to ask fewer questions during visits with a health careprovider [52]. However, a low educational level does notnecessarily implicate low learning capacity. Older women inparticular might not have had the opportunity to proceed to highereducation. Differences between the effects of HL and education onperceived information provision found in this study may thereforebe partially explained by misclassication of women in the loweducation group.

    Another explanation could be that low educated women hadlower information needs and were less critical than highlyeducated women. This may have caused them to feel that theyreceived a large amount of disease-related information, while theactual amount of information was more or less equal in bothgroups. Finally, it has been suggested that low educated patients

    al level and subjective health literacy with perceived level of information provision.

    ghb

    Medium HL Low HL R2 (%) DR2 (%) Dp-value

    10.3% 4.1%

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    e

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    uc

    s;

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    PEC-4748; No. of Pages 8generally tend to report more positive health care experiencescompared to highly educated patients, which may reect areporting bias rather than a real difference [53,54].

    Subjective HL and educational level accounted for a remarkablysmall amount of the variability in the outcome variables. There areseveral factors other than subjective HL and education that mayhave had an impact on patients perceived level of informationprovision and satisfaction. We controlled for the potentialconfounders tumor type, years since diagnosis, age at time ofsurvey, employment status, and marital status. However, differ-ences in information needs may have affected the outcomes aswell. How information needs are related to HL and the outcomevariables, e.g. through mediation or as a confounding factor,remains uncertain. Another patient characteristic that might haveaffected the outcomes is coping style. Two main coping styles fordealing with cancer information have been described: monitoring(attending to) and blunting (avoiding). Patients with a monitoringstyle tend to do better when provided with more information, andpatients with a blunting style generally fare better when given lessinformation [55]. A recent study found that cancer patients with acombination of the personality traits negative affectivity and socialinhibition (the so-called Type D personality) reported that theyreceived less information about their disease, medical tests, andtreatment, and were less satised with the information receivedcompared to non-Type D patients [56]. This indicates thatpersonality could play a signicant role in cancer patientsperceived level of information provision and satisfaction. More-over, differences in actual information receipt could have directlyaffected patients perceived level of information provision andsatisfaction.

    Another explanation for the small amount of variabilityexplained in the regression analyses may lie in the measurementof HL. HL was measured by asking patients perceived condence(self-efcacy) and not their actual skills in lling out medical formsby themselves [57]. As patients with low literacy skills tend tooverestimate their own abilities [58], this could have affected theprevalence rate of low HL. Future research on the relation betweenHL and information provision may be improved by addressing

    Table 4Hierarchical multiple logistic regression analyses evaluating the associations of educat

    unsatised (not or only a little satised with the information received; reference) an

    High

    educationaMedium education Low educati

    Model 2 (odds ratio, 95% CI) Ref 0.5 (0.2; 1.1) 1.1 (0.4; 3.3Model 3 (odds ratio, 95% CI) Ref 0.6 (0.3; 1.2) 2.0 (0.6; 6.8

    Note: Model 1 includes tumor type, years since diagnosis, age at time of survey, employm

    educational level; Model 3 includes all of Model 2 as well as subjective health literaa Educational level: high = university or higher education; medium = secondary edb HL = subjective health literacy: high = being very condent lling out medical form

    little or not at all condent lling out medical forms.* p < 0.01.objectively measured HL, for example by using validated versionsof the REALM (Rapid Estimate of Adult Literacy in Medicine) [59],the S-TOFHLA (Short Test of Functional Health Literacy in Adults)[60] or the NVS (Newest Vital Sign) [61]. Of these instruments, theREALM and the NVS have already been adapted and applied in theNetherlands [34]. However, it is unclear whether these generic HLmeasures cover all important skills needed for cancer survivors tond their way in cancer care. Future studies should investigatewhether a cancer-specic HL instrument is needed to measure thebroad scope of cancer-related HL.

    The present study is one of the rst studies in the eld of cancercare examining the association between HL and informationprovision. However, some limitations should be considered wheninterpreting the results. One limitation concerns the relatively low

    Please cite this article in press as: Verkissen MN, et al. The role of heamong women with ovarian tumors: A study from the populatiodx.doi.org/10.1016/j.pec.2014.03.008response rate (50%), which increases the likelihood of selectionbias. It is also reasonable that the mean time since diagnosis of 6.3years has affected the recall of information received. We thereforecontrolled for years since diagnosis in our analyses. Furthermore,information satisfaction was measured by using only one itemwhich we dichotomized for the analyses. The test-retest reliabilityand the convergent and divergent validity of this question haveshown to be good [41], but have not been evaluated for thedichotomized item. Moreover, the question does not provideinformation as to why patients were (un)satised with theinformation they received.

    The provision of information to BOT survivors may differsubstantially from the provision of information to ovarian cancersurvivors. Unlike invasive ovarian tumors, BOT rarely metastasize,are usually slow growing, and are not likely to lead to death.Furthermore, BOT generally are treated by surgery alone, becausethey are insensitive to chemotherapy. Because we expected tumortype (ovarian cancer versus BOT) to be related to informationprovision, we adjusted for tumor type in the regression analyses.For future research, it might be of interest to compare ovariancancer and BOT survivors in their information provision and itsrelationship with HL and education. This may help understand howinformation provision might differ between medical conditions.

    4.2. Conclusion

    Ovarian cancer and BOT survivors with low subjective HLreported that they received less information about medical testsperformed in relation to their disease, and were less likely to besatised with the information received compared to survivors withhigh subjective HL.

    These associations were found after controlling for educationallevel, showing that HL is related to perceived informationprovision and satisfaction beyond the effect of education.

    However, HL accounted only for a small amount of thevariability in information provision. A more objective cancer-specic measure of HL might be more appropriate to measurecancer-related HL and its association with cancer-specic infor-

    nal level and subjective health literacy with information satisfaction, categorized as

    satised (quite or very satised with the information received).

    High HLb Medium HL Low HL 2LL D2LL Dp-value

    291.7 5.1 0.08

    Ref 0.9 (0.5; 1.7) 0.2 (0.1; 0.6)* 282.1 9.7

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    PEC-4748; No. of Pages 8before they leave the consultation (the teach-back technique) toensure that patients understand what they have been told [63,64].For future research, it is important to evaluate the effectiveness ofsuch strategies in the information provision to cancer survivorswith low HL.

    Role of funding source

    The present study was supported with grant no. UVT 2010-4743 from the Dutch Cancer Society and an investment grant of theNetherlands Organization for Scientic Research (NWO #480-08-009), The Hague, the Netherlands. The funding source had noinvolvement in the study design, the collection, analysis, andinterpretation of data, the writing of the manuscript, and thedecision to submit the paper for publication.

    Authors contributions

    MV, NE, MF, MLE-B, MA, CV, and OH contributed to the conceptand design of the study. MF and MLE-B provided advice on HLmeasurement. NE, KN, and CV contributed to the acquisition of thedata. MV and NE analyzed the data and drafted the manuscript. Allauthors provided input into revisions of the manuscript and haveapproved the nal manuscript.

    Conict of interest

    None.

    Acknowledgements

    We would like to thank all patients and their doctors for theirparticipation in the study. In addition, we want tothank the followinghospitals for their cooperation: Amphia Hospital, Breda; CatharinaHospital, Eindhoven; St. Elisabeth Hospital, Tilburg; Jeroen BoschHospital, s Hertogenbosch; TweeSteden Hospital, Tilburg.

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    PEC-4748; No. of Pages 8Please cite this article in press as: Verkissen MN, et al. The role of heamong women with ovarian tumors: A study from the populatiodx.doi.org/10.1016/j.pec.2014.03.008alth literacy in perceived information provision and satisfactionn-based PROFILES registry. Patient Educ Couns (2014), http://

    The role of health literacy in perceived information provision and satisfaction among women with ovarian tumors: A study from the population-based PROFILES registryIntroductionMethodsSetting and participantsData collectionMeasuresClinical and socio-demographic characteristicsSubjective health literacyPerceived information provision and satisfaction

    Statistical analyses

    ResultsPatient characteristicsSubjective health literacy and educational levelEducational level, subjective health literacy, and perceived information provisionEducational level, subjective health literacy, and information satisfaction

    Discussion and conclusionDiscussionConclusionPractice implications

    Role of funding sourceAuthors contributionsConflict of interestAcknowledgementsReferences