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7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 111
The trajectories of adolescent anxiety and depressive symptoms over
the
course
of
a
transdiagnostic
treatment
Alexander H Queen a David H Barlowb Jill Ehrenreich-MayaaDepartment of Psychology University of Miami United StatesbCenter for Anxiety and Related Disorders Boston University United States
A R T I C L E I N F O
Article history
Received 31 January 2014Accepted 12 May 2014
Available online 2 June 2014
Keywords
Anxiety
Depression
Adolescence
Transdiagnostic
Treatment
A B S T R A C T
Anxiety and depressive disorders commonly co-occur during adolescence sharemultiple vulnerability
factors and respond to similar psychosocial and pharmacological interventions However anxiety anddepression may also be considered distinct constructs and differ on some underlying properties Prior
research efforts on evidence-based treatments for youth have been unable to examine the concurrent
trajectories of primary anxiety and depressive concerns across the course of treatment The advent of
transdiagnostic approaches for these emotional disorders in youth allows for such examination The
present study examined the separate trajectories of adolescent anxiety and depressive symptoms over
the course of a transdiagnostic intervention the Uni1047297ed Protocol for the Treatment of Emotional
Disordersin Adolescence (UP-A Ehrenreich et al 2008) aswell asupto sixmonths followingtreatment
The sample included 59 adolescents ages 12ndash17 years old (M =1542 SD= 171) who completed at least
eight sessions of the UP-A as part of an open trial or randomized controlled trial across two treatment
sites Piecewise latent growth curve analyses found adolescent self-rated anxiety and depressive
symptoms showed similar rates of improvement during treatment but while anxiety symptoms
continued to improve during follow-up depressive symptoms showed non-signi1047297cant improvement
after treatment Parent-rated symptoms also showed similar rates of improvement for anxiety and
depression during the UP-A to those observed for adolescent self-report but little improvement after
treatment across either anxiety or depressive symptoms To a certain degree the results mirror thoseobservedamong otherevidence-based treatments for youthwithanxietyanddepression though results
hold implications for future iterationsof transdiagnostictreatmentsregarding optimization of outcomes
for adolescents with depressive symptoms
atilde 2014 Elsevier Ltd All rights reserved
1 Introduction
Anxiety
disorders
are
the
most
prevalent
psychiatric
disorders
in adolescence with prevalence estimates of 10ndash21 in the general
population in the United States (Costello Mustillo Erkanli Keeler
amp
Angold
2003)
Considered
through
the
lens
of
DSM-IV
(American
Psychiatric
Association
2000) unipolar
depressive
disorders (ie major depressive disorder [MDD] dysthymic
disorder) as a whole are also common mental health conditions
and
become
more
prevalent
during
adolescence
as
compared
to
earlier
in
development
(Costello
et
al
2002)
Anxiety
and
depressive disorders commonly co-occur with one another in
adolescence Between 16 and 62 of youth with an anxiety
disorder also meet criteria for depression with the highest
comorbidity
rates
found
among
treatment-seeking
adolescents
(Brady
amp
Kendall
1992 Ollendick
Shortt
amp
Sander
2005)
In
addition self-report measures of youth anxiety and depressive
symptoms show moderate correlations with one another (eg
r
=
034)
even
after
controlling
for
overlapping
items
on
these
instruments
(Stark
amp
Laurent
2001)
In addition to their high comorbidity with one another youth
anxiety and depression share a number of biological environmen-
tal
and
psychological
risk
factors
(for
a
more
thorough
review
see
Garber
amp
Weersing
2010) For
instance
behavioral
inhibition
in
early childhood is a risk factor for the later development of both
anxiety and depression (Kagan Reznick amp Snidman 1987) and
both anxiety and depressive disorders are associated with
neuroendocrine
(Dahl
et
al
2000 Weems
Zakem
Costa
Cannon
amp Watts 2005) and neurotransmitter dysregulation (Flores et al
2004 Fox et al 2005) In addition high negative affect (NA) has
shown to be a latent factor underlying all of the anxiety and
Corresponding author at Department of Psychology University of Miami Flipse
315 5665 Ponce de Leon Boulevard Coral Gables FL 33146 United States
E-mail address jehrenreichpsymiamiedu (J Ehrenreich-May)
httpdxdoiorg101016jjanxdis201405007
0887-6185atilde 2014 Elsevier Ltd All rights reserved
Journal of Anxiety Disorders 28 (2014) 511ndash521
Contents
lists
available
at
ScienceDirect
Journal of Anxiety Disorders
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 211
depressive disorders (Brown Chorpita amp Barlow 1998 Trosper
Whitton Brown amp Pincus 2012)
Youth anxiety and depressive disorders also demonstrate
similar responses to pharmacological and psychosocial interven-
tions For instance both anxiety and depression are responsive to
selective serotonin reuptake inhibitor (SSRI) medications (eg
Treatment for Adolescents with Depression Study (TADS) Team
2004 Walkup et al 2008) Prior work with cognitive-behavioral
therapy (CBT) trials have found ldquospill-overrdquo effects onto comorbid
anxiety or depressive disorders regardless of the principal
disorder For example anxiety-focused CBT has demonstrated
positive effects on comorbid depressive symptoms (Kendall
Safford Flannery-Schroeder amp Webb 2004) and a meta-analysis
of CBT for youth depression found effect sizes in anxiety symptom
reduction (ES = 039) that were only slightly less than those for
depressive symptom improvement (ES = 057 Weisz McCarty amp
Valeri 2006)
Given their frequent comorbidity shared vulnerability factors
and similar response to treatment some (eg Barlow Allen amp
Choate 2004) have advocated for a transdiagnostic or disorder-
non-speci1047297c treatment approach that targets higher-order psy-
chological factors common to the emotional disorders Such an
approach is hypothesized to allow for greater clinical
1047298exibility and
use with patients presenting with multiple emotional disorders aswell as reduce clinician burden in learning multiple disorder-
speci1047297c treatment manuals (McHugh amp Barlow 2010) As such
recent clinical research has focused upon the development and
evaluation of transdiagnostic treatments that may effectively
target anxiety and depressive disorders within a single protocol
The Uni1047297ed Protocol for the Treatment of Emotional Disorders
in Adolescence (UP-A Ehrenreich et al 2008) is a developmental
adaptation of the adult Uni1047297ed Protocol (UP Barlow et al 2010)
designed for adolescents ages 12ndash17 years old presenting with any
primary anxiety disorder unipolar depressive disorder or their
combination The UP-A has theoretical roots in emotion regulation
cognitive science and behavior modi1047297cation and distills common
evidence-based
techniques
that
cut
across
disorder-speci1047297c
treatment manuals for youth anxiety and depression (egpsychoeducation non-judgmental awareness cognitive reapprais-
al exposure behavioral activation etc) within a singular protocol
The
UP-A
incorporates
standard
evidence-based
principles
within
the
broader
function
context
and
regulation
of
a
range
of
positive
and negative emotions (eg sadness anger fear) Therefore it is
theorized to positively affect how adolescents attend to modulate
and
experience
emotions
that
cut
across
speci1047297c
disorders
Similar
to
the
UP
the
UP-A
targets
1047297ve
higher-order
principles
thought
to
be latent constructs underlying lower-order speci1047297c anxiety and
depressive disorders (1) increase present-focused awareness of
emotions
(2)
enhance
cognitive
1047298exibility
(3)
prevent
emotional
avoidance
and
maladaptive
emotion-driven
behaviors
(4)
increase
acceptance of uncomfortable emotion-related physiological sen-
sations
and
(5)
facilitate
exposure
to
bodily
and
environmentaltriggers
of
emotional
experiences
(Barlow
et
al
2010)
A prior
open
trial
of
the
UP-A
established
initial
ef 1047297cacy
with
subjects demonstrating signi1047297cant pre-post reductions in clini-
cian-rated diagnostic severity across anxiety and depressive
disorder
diagnoses
(Trosper
Buzzella
Bennett
amp
Ehrenreich
2009)
and
an
immediate
treatment
(TX)
condition
of
the
UP-A
has found to outperform an 8-week treatment-delayed waitlist
(WL) condition in clinician-rated diagnostic severity for the
principal
disorder
in
a
recently
completed
randomized
controlled
trial
(RCT
Ehrenreich-May
Queen
Rodriguez
amp
Rosen1047297eld
2012)
Analyses from this RCT also found that the presence of a depressive
disorder did not moderate treatment outcomes in the UP-A
(Ehrenreich-May
et
al
2012)
whereas
many
previous
CBT
trials
for
youth
anxiety
have
found
poorer
outcomes
for
patients
with
comorbid depression (eg Berman Weems Silverman amp Kurtines
2000 Ginsburg et al 2011 OrsquoNeil amp Kendall 2012)
To summarize youth anxiety and depression are known to
commonly co-occur with one another share multiple vulnerability
factors and may be effectively treated with a uni1047297ed treatment
approach However despite their similarities anxiety and depres-
sion have also shown to be distinct constructs For instance factor
analytic studies with school-based (Crowley amp Emerson 1996) and
clinical samples (Stavrakaki Vargo Boodoosingh amp Roberts 1987)
have found stronger support for two-factor models of anxiety and
depression compared to single factor models In addition while
both anxiety and depression are characterized by high negative
affect low positive affect has shown stronger associations with
depressive symptoms than with anxiety symptoms (for more
comprehensive reviews see Anderson amp Hope 2008 De Bolle amp De
Fruyt 2010) Given these important differences a next step in
investigating transdiagnostic treatment approaches is to examine
the separate trajectories of symptom change for anxiety and
depression over the course of treatment in order to assess if they
show similar or differential rates of change
The present study examined the separate trajectories of anxiety
and depressive symptoms over the course of the UP-A and up to
six months following the end of treatment for adolescent subjects
completing the UP-A as part of the open trial or RCT investigationWe used piecewise latent growth curve modeling (LGCM) to model
these trajectories over two separate time periods during the
course of treatment (ldquotreatment sloperdquo) and up to six months after
treatment ended (ldquofollow-up sloperdquo) Piecewise LGCM is often
recommended when examining change during treatment and
follow-up given likely non-linear change (Brown 2004) Separate
models were conducted for anxiety and depressive symptoms
Separate models were also conducted for self-rated and parent-
rated symptoms in order to examine informant differences in
symptom change trajectories Therefore a total of four piecewise
LGCMs were conducted
2
Method
21 Participants
Participants
were
59
adolescents
(576
female)
ages
12ndash17
years
old
(M
=
1542
SD
=
171)
who
received
at
least
eight
sessions
of the UP-A and completed at least one post-baseline assessment
Given the aim of the study was to examine separate trajectories of
anxiety
and
depression
symptom
change
for
those
completing
the
intervention
we
decided
to
restrict
analyses
to
those
receiving
at
least 8 sessions as this represented the minimum dosage possible
to be considered a treatment completer This subsample of 59
participants
was
culled
from
a
total
sample
of
67
participants
who
were
enrolled
in
either
the
open
trial
or
RCT
investigation
of
the
UP-A Eight (1194) of the 67 participants that did not complete at
least
eight
sessions
of
the
intervention
were
part
of
the
open
trial(n
=
2)
or
RCT
(n
=
6)
respectively
and
did
not
have
any
post-
baseline
assessment
data
T -test
and
chi-square
analyses
revealed
that those completing at least eight sessions (n = 59) did not
signi1047297cantly differ from those who dropped out prior to eight
sessions
(n
=
8)
with
regard
to
age
gender
ethnicity
severity
of
principal
diagnosis
depressive
disorder
comorbidity
status
or
baseline levels of anxiety or depressive symptoms (child or parent
report)
Participants
were
evenly
divided
between
HispanicLatino
(n
=
26
441)
and
White
Non-Hispanic
ethnicities
(n
=
26
441) The remaining subjects identi1047297ed themselves as having
BlackAfrican-American (n = 2 34) Asian-American (n = 1 17)
and
ldquootherrdquo ethnicity
(n
=
4
68)
The
median
reported
annual
family
income
was
$100000
(SD
=
$80000)
The
majority
of
512 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 311
participants had parents who were married (n = 40 678)
Remaining participants had parents who were separateddivorced
(n = 13 2203) widowed (n = 2 34) or never married (n = 4
678)
Eligibility requirements for both the open trial and RCT
included being between 12 and 17 years old (participants could
be 18 if they were still in high school) and having a primary
diagnosis of any DSM-IV anxiety andor unipolar depressive
disorder Adolescents with other psychiatric dif 1047297culties including
attention-de1047297cithyperactivity disorder (ADHD) eating disorders
and non-treatment-interfering substance abuse were eligible for
participation However the primary diagnosis had to be an anxiety
or depressive disorder Exclusion criteria included bipolar disorder
treatment-interfering substance abuse severe suicidal ideation or
recent psychiatric hospitalization treatment-interfering cognitive
functioning (eg IQ below 80) and a prior course of CBT for anxiety
or depression Participants and at least one parent were also
required to read and comprehend English well enough to complete
study measures Those concurrently receiving psychiatric medica-
tion were required to have been on a stable dosage of an SSRI
medication for three months andor a stable dosage of benzodiaz-
epine medication for one month prior to study enrollment
Adolescents completing the UP-A as part of the open trial
participated at a university-based clinic in a large urban area in theNortheastern United States (n = 15) while those in a subsequent
RCT participated at a university-based clinic in a large urban area in
the Southeastern United States (n = 44) There were no signi1047297cant
site differences with regard to gender depressive disorder
comorbidity treatment length or severity of anxiety and depres-
sive symptoms However subjects in the RCT were slightly older
(M = 1569 SD = 170) than open trial participants (M
= 1463
SD = 155) t (57) = 213 p = 004 d = 064 In addition as expected
based upon demographic characteristics of the surrounding
communities RCT participants were more likely to be Hispanic
Latino (6136) whereas all of the open trial participants were
White Non-Hispanic x2 (3) = 2553 p lt 0001 There were no
differences
among
ethnicities
with
regard
to
any
study
variables
at
any time pointsPrincipalco-principal diagnoses and comorbid diagnoses at
baseline are displayed in Table 1 (Diagnoses assigned as co-
principal
are
included
for
totals
within
the
principal
diagnosis
category)
The
most
common
principal
diagnoses
were
generalized
anxiety disorder (n = 23 3898) followed by social phobia (n= 19
3220) and major depressive disorder (n = 11 1864) Sixteen
participants (2712) were assigned co-principal diagnoses with
the most common combination being generalized anxiety disorder
and social phobia (n = 4) All of the DSM-IV anxiety disorders were
represented with either a principalco-principal or comorbid
diagnosis including obsessive-compulsive disorder (n = 8 1356)
panic disorder (n = 7 1186) speci1047297c phobia (n = 8 1356)
separation anxiety disorder (n = 2 339) and post-traumatic
stress disorder (n = 1 169)
The great majority of participants (n = 47 797) were assigned
a primary anxiety disorder diagnosis while nine participants
(153) received a primary depressive disorder diagnosis and three
participants (51) were assigned co-principal anxiety and
depressive disorder diagnoses Although only 12 participants
(2034) received a principal or co-principal depressive disorder
diagnosis comorbid depression was well-represented with 23
participants (3898) assigned a secondary comorbid depressive
disorder Therefore the majority of participants (n = 35 6102)
were assigned a depressive disorder The majority of those with a
depressive disorder were diagnosed with major depressive
disorder (n = 25) although dysthymic disorder (n = 5) and depres-
sive disorder not otherwise speci1047297ed (NOS
n = 6) were also
present (One participant was diagnosed with both major
depressive disorder and dysthymic disorder) In addition toanxiety and depression comorbidity other psychiatric conditions
were also present including ADHD (n = 4 678) oppositional-
de1047297ant disorder (n = 1 169) and eating disorder NOS (n = 1
169) No participants were assigned a diagnosis of a current
substance abuse disorder
The majority of participants (n = 46 78) were not currently
taking psychiatric medication at the time of the study Seven
participants (1186) were taking a SSRI medication alone one
participant (169) was taking benzodiazepine alone and two
participants (339) were taking both an SSRI and benzodiaze-
pine With regard to stimulant medication for ADHD symptoms
two participants (339) were taking a stimulant medication
alone
while
one
participant
(169)
was
taking
a
stimulant
medication in combination with an SSRI medication Analyses of those taking medication (n = 13) compared to those not taking
medication (n = 46) revealed no signi1047297cant differences on any
baseline
variables
In
addition
medication
status
was unrelated
to
anxiety
or
depressive
symptom
severity
during
treatment
or
at
follow-up
Table 1
Frequencies of diagnoses at baseline
Diagnosis Principal diagnosis ()a Comorbid diagnoses () Total ()
Generalized anxiety disorder 23 (3898) 15 (2542) 38 (6441)
Social phobia 19 (3220) 7 (1186) 26 (4407)
Major depressive disorder 11 (1864) 14 (2373) 25 (4237)
Obsessive-compulsive disorder 4 (678) 4 (678) 8 (1356)
Panic disorder with agoraphobia 3 (508) 3 (508)
Speci1047297c phobia 3 (508) 5 (847) 8 (1356)
Panic disorder without agoraphobia 2 (339) 2 (339) 4 (678)
Tic disorder 1 (169) 1 (169)
Anxiety disorder NOS 5 (847) 2 (339) 7 (1186)
Dysthymic disorder 2 (339) 3 (508) 5 (847)
Trichotillomania 1 (169) 1 (169)
ADHD combined type 1 (169) 2 (339) 3 (508)
Separation anxiety disorder 2 (339) 2 (339)
Depressive disorder NOS 6 (1017) 6 (1017)
Post-traumatic stress disorder 1 (169) 1 (169)
Enuresis 1 (169) 1 (169)
ADHD inattentive type 1 (169) 1 (169)
Oppositional-de1047297ant disorder 1 (169) 1 (169)
Eating disorder NOS 1 (169) 1 (169)
a Percentages do not add to 100 because some subjects had co-principal diagnoses
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 513
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 411
22 Procedure
The Institutional Review Boards of the two universities
participating in this trial granted approval for the study
Adolescents were referred for evaluation and treatment services
at the clinics by school personnel pediatricians psychiatrists
other mental health care professionals community agencies or
were self-referred through community online or radio advertise-
ments Upon contacting the clinic the adolescentrsquos parent
completed an initial telephone screen to assess primary concerns
and rule out exclusionary criteria If the primary concern was
determined to be anxiety or mood related the adolescent and
parent were scheduled for an in-person diagnostic evaluation at
the clinic Parents of adolescents not deemed eligible were
provided with appropriate treatment referrals
Fig 1 displays the CONSORT diagram outlining participant
recruitment and assignment At the initial diagnostic evaluation
the adolescent and parent separately completed the Anxiety
Disorders Interview Schedule for the DSM-IV Child Version Parent
and Child Reports (ADIS-IV-CP Silverman amp Albano 1996) with a
PhD-level clinical psychologist or doctoral student in clinical child
psychology In addition the adolescent and parent completed
paper-and-pencil questionnaires at this evaluation After obtaining
both parental consent and adolescent assent the adolescentparticipated in the ADIS-IV while the parent completed measures
in the waiting room Similarly the adolescent completed their
measures while the parent completed their interview Symptom
data collected at this initial diagnostic evaluation were used as
Time 1 data for subjects in the open trial and for those in the TX
condition in the RCT
Following the diagnostic evaluation clinician-rated composite
diagnoses were assigned by compiling information from adoles-
cent and parent responses to ADIS-IV-CP The assessor assigned a
clinical severity rating (CSR) value an indicator of diagnostic
severity and impairment to every composite diagnosis CSR values
can range from 0 to 8 with values 4 indicating clinical levels of
impairment
Only
participants
receiving
a
primary
diagnosis
of
an
anxiety or depressive disorder assigned a CSR 4 were eligible toparticipate in UP-A trial Final diagnoses and CSR values were
con1047297rmed at a weekly supervision meeting On average partic-
ipants
presented
with
moderately
severe
impairment
with
regard
to
their
primary
anxiety
or
depressive
disorder
diagnosis
(M
=
581
SD = 078 range = 4ndash7)
Adolescents assigned a primary diagnosis of an anxiety or
depressive
disorder
and who
did not
meet exclusion
criteria
were
eligible
to
enroll
in
treatment
trial Upon
obtaining
written
parental consent and adolescent assent participants in the RCT
were randomized to either the TX or the WL condition
Participants
in
the
open trial
and
TX
arm
of
the
RCT
began
treatment
immediately
All
participants and
their parent
com-
pleted symptom measures at Time 2 (8 weeks after beginning
treatment
considered
the ldquomid-treatment
rdquo
point for most)
Time3
(end
of
treatment) Time 4
(three
months after
treatment
termination)
and
Time 5
(six
months after
treatment
termina-
tion)
Participants in the WL condition did not receive treatment
during
the
8-week
WL period
but
did
brief
telephone
ldquocheck-insrdquo
with
their
assigned
therapist
to
assess
for
clinical
deterioration
every other week At the end of the WL period participants and
their parent completed symptom measures at the clinic These data
were
used
as
Time
1
data
for
WL
participants
Analyses
revealed
no
signi1047297cant
changes
in
WL participantsrsquo
data
from
initial
diagnostic
evaluation to the end of the WL period on symptom measures all
prsquos gt 020 Participants in the WL arm then began UP-A and
completed
assessments
at
same
intervals
as
those
in
the
open
trial
and
TX
arm
of
RCT
221 Treatment structure and content
The UP-A follows a principle-based
1047298exible treatment struc-
ture The intervention can be delivered over a varying length of
time (between 8 and 21 weekly sessions administered in an
individual format) There are 1047297ve required modules which
correspond to the
1047297ve core principles underlining the UPUP-A
(Barlow et al 2010) Therapists are allowed to devote more
sessions to a required module dependent upon patient needs but
ideally all modules are completed during the course of treatment
Therefore while treatment length may differ among patients all
subjects receive the same
1047297ve core modules and relevant skills
(eg psychoeducation non-judgmental awarenessmindfulness
cognitive reappraisal exposure behavioral activation) See Table 2
for a display of the
1047297ve required modules and suggested session
length for each module including treatment skills delivered within
each module and the corresponding UPUP-A core principles
targeted Importantly one of the unique features of the UP models
is the ability to target emotion regulation de1047297cits across a broader
range of positive and negative emotions compared to traditional
disorder-speci1047297c treatment manuals
In addition to the 1047297verequired modules three optional modules
are available to the therapist as needed to address parenting skills
motivational enhancement and clinical deterioration and can be
used at any point in treatment At least one parent is required to beactively involved in treatment While some variability is allowable
typically a parent is involved in the last 10ndash15min of every session
to review content and the assigned homework Individual sessions
with the parent may be used as part of an optional module if the
therapist feels that certain parenting behaviors (eg overprotec-
tion high criticism parentndashteen con1047298ict etc) are counterproduc-
tive to treatment progress or as needed for exposure planning
Motivational interviewing (Miller amp Rollnick 2002) techniques can
be used in sessions as part of a second optional module for
adolescents who appear reluctant to engage in treatment Finally
sessions within the third optional module can be used to develop a
safety plan with the adolescent and his or her parent in the event
the
patient
experiences
impulses
for
self-harm
However
adoles-
cents who show immediate risk for suicide or other pronouncedclinical deterioration could also be discontinued from UP-A studies
and referred for more intensive services if appropriate
23
Measures
231 Anxiety Disorders Interview Schedule for DSM-IV-childparent
version
(ADIS-IV-CP
Silverman
amp
Albano
1996)
The
ADIS-IV-CP
was
completed
at
the
adolescentrsquos
baseline
assessment to determine diagnostic eligibility The ADIS-IV-CP is a
semi-structured diagnostic interview for children and adolescents
ages
7ndash17years
that
assesses
all
DSM-IV
anxiety
disorders
The
ADIS-
IV-CP
also
assesses
for
unipolar
depressive
disorders
and
external-
izing disorders (ie ADHD oppositional-de1047297ant disorder conduct
disorder)
and
screens
for
substance
abuse
schizophrenia
pervasivedevelopmental
disorders
eating
disorders
and
somatoform
dis-
orders
In
addition
participants
were screened
for
bipolar
disorder
Inter-rater reliability for the primary diagnosis within this sample
was very good (k= 82 p lt 0001) All assessors were previously
trained
in
ADIS-IV-CP
administration
and
participated
in
weekly
supervision
meetings
led
by
the
third
author
(JEM)
After
an
initial
training workshop new examiners were required to reach
agreement on all clinical diagnoses and CSR levels (ie within 1
CSR
value)
with
an
expert
rater
(JEM)
on
three
consecutive
assessments
before
conducting
interviews
independently
232 Revised Childrenrsquo s Anxiety and Depression Scale
Subjects
completed
the
Revised
Childrenrsquos Anxiety
and
Depression
Scale
(RCADS
Chorpita
Yim
Mof 1047297tt
Umemoto
amp
514 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 511
A s s e s s e
d
f o r e l i g i b i l i t y ( n = 1 2 2 )
E x c l u d e d
o r D e c l i n e d ( n = 5 5 )
D i d n o t
m e e t
i n c l u s i o n c r i t e r i
a
S o u
g h t t r e a t m e
n t e l
s e w h e r e
O p t e d f o
r p r i
v a
t e t r e a t m e n t
D a t a
A v a i l a b l e
8 -
W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 2 0
)
3 M o n t h F o l
l o w
- U p ( n = 1 0
)
6 M o n t h F o l
l o w
- U p ( n = 1 1
)
E n r o l
l e d i n
R C T a n d r
a n d o m i z e d t o T X
( n = 2 6 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n
= 2 3
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n
= 3 )
D a t a a v a i l a b l e
8 - W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 1 5
)
3 M o n t h F o l
l o w
- U p ( n = 8 )
6 M o n t h F o l
l o w
- U p ( n = 6 )
E n r o l
l e d i n
R C T a n d r a n d o m i z e d t o
W
L
( n = 2 4 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n = 2 1
)
D i d n o t r
e c e i v e
a t l e a s t 8
s e s s
i o n s
( n = 3 )
E n
r o l
l e d ( n
= 6 7
)
E n r o l
l e d i n o p e n t
r i a l (
n = 1 7
)
R e c e i v e d
a t
l e a s t 8 s e s s
i o n s
( n = 1 5
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n = 2 )
D a t a
a v a i l a b l e
8 - W e e
k ( n
=
1 5
)
E n d o f T r e a t m e n t ( n
= 1 3
)
3 M o n t h
F o l
l o w
- U p
( n = 1 1
)
6 M o n t h
F o l
l o w
- U p
( n = 7 )
F i g
1
U P - A C O N S O R T 1047298 o w
d i a g r a m
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 515
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 611
Francis 2000) at all
1047297ve time points The RCADS is a 47-item self-
report measure of anxiety and depressive symptoms that containssix distinct subscales based upon DSM-IV criteria separation
anxiety social phobia generalized anxiety disorder obsessive-
compulsive disorder panic disorder and major depressive disor-
der Respondents are asked to indicate how much each item
describes them using never (0) sometimes (1) often (2) or always
(3) A Total Anxiety subscale score is comprised of 37 items and
summed from responses to the
1047297ve anxiety subscales A major
depressive disorder (MDD) subscale score is comprised of 10 items
Raw
scores
were
converted
to
T -scores
using
child
age
and
gender
to place the two subscales on the same metric with
T-scores of 65
or greater indicating borderline levels of clinical severity and T-
scores of 70 and above representing clinically signi1047297cant elevations
(Weiss
amp
Chorpita
2011)
Internal
consistency
values
for
the
RCADS
Total Anxiety subscale were as follows a= 094 at Time 1 a= 095at Time 2 a= 091 at Time 3 a= 087 at Time 4 and a= 093 at Time
5 Internal consistency values for RCADS MDD subscale were as
follows
a=
085
at
Time
1 a=
090
at
Time
2
a=
091
at
Time
3
a=
091
at
Time
4
and a=
093
at
Time
5
233 Revised childrenrsquo s anxiety and depression scales ndash parent
version
The
adolescentrsquos parent
completed
the
Revised
Childrenrsquos
Anxiety and Depression Scales-Parent version (RCADS-P Ebesu-
tani Bernstein Nakamura Chorpita amp Weisz 2010) at all 1047297ve time
points
The
RCADS-P
is
a
47-item
parent-rated
measure
of
their
childadolescentrsquos
anxiety
and
depressive
symptoms
The
RCADS-P
contains the same six subscales as the RCADS and has previously
shown
good
psychometric
properties
with
school-based
(Ebesu-tani
et
al
2011)
and
clinical
samples
(Ebesutani
et
al
2010) For
the
current
sample
internal
consistency
values
for
RCADS-P
Total
Anxiety subscale were as follows a= 092 at Time 1 a= 091 at
Time 2 a= 094 at Time 3 a= 078 at Time 4 and a= 088 at Time 5
Internal
consistency
values
for
the
RCADS-P
MDD
subscale
were
as
follows
a=
078
at
Time
1
a=
088
at
Time
2
a=
091
at
Time
3
a= 060 at Time 4 and a= 092 at Time 5
24
Data
analytic
plan
For the present study we used piecewise LGCM to model
symptom trajectories over (1) the course of treatment and (2)
during the
six-month
follow-up
period
Several
indices
of
model
1047297t
were
used
including
chi square
comparative 1047297x index
(CFI)
root mean square error of approximation (RMSEA) and stan-
dardized root mean square residual (SRMR) For purposes of interpretation indices of good model 1047297t include a non-signi1047297cant
chi square ( p gt 005) CFI gt 095 RMSEA
lt 006 and SRMR lt 008
(Kline 2011) Signi1047297cant tests for parameter estimates were
conducted with the z -statistic using a two-tailed test LGCM
analyses were conducted using MPLUS Fifth version (Muthen amp
Muthen 2005)
3 Results
The data were
1047297rst screened for normality and to determine if
there were any statistical outliers Skewness and kurtosis levels
were within acceptable ranges (Kline 2011) No signi1047297cant
outliers ( z
3)
were
identi1047297ed
at
any
time
points
All
subjects
had complete data for Time 1 as well as at least one other post-baseline assessment Fifty-1047297ve subjects (9322) had data at the 8-
week assessment (Time 2) and 48 participants (8136) had data at
the
end
of
treatment
(M
=
1558
sessions)
assessment
(Time
3)
However
there
was
considerable
missing
data
at
the
two
follow-
up time points with 29 subjects (4915) having available data
three months after treatment (Time 4) and 24 participants
(4068)
having
data
six
months
after
treatment
(Time
5)
although
6271
of
subjects
had
available
data
for
at
least
one
follow-up time point Attrition analyses revealed no signi1047297cant
differences between those with complete data and those with
missing
data
on
any
indicators
of
symptom
severity
at
baseline
or
any
demographic
variables
(eg
age
gender
ethnicity)
Further-
more those with and without follow-up data did not show
signi1047297cant
differences
on
any
variables
at
the
post-treatmentassessment
31 Descriptive statistics
See
Table
3
for
observed
means
and
standard
deviations
of
RCADSRCADS-P
Total
Anxiety
T -scores
and
RCADSRCADS-P
MDD
T -scores at each time point In addition the percentage of
participants with T -scores 65 and T -scores 70 are presented
Mean
T -scores
on
all
four
measures
reduced
to
below
65
by
Time
3
indicating
that
mean
levels
of
both
self-rated
and
parent-rated
anxiety and depressive symptoms were within the normative
range by the end of treatment Analysis of percentages of
participants
with
T -scores
65
and
T -scores
70
also
revealed
reductions
in
those
with
borderline
elevated
and
clinically
elevated
Table 2
UP-A structure and content
Required
module
Suggested
number of
sessions
Techniquesskills Core UPUP-A principle(s) targeted
1 1ndash3 Psychoeducation of emotions functional assessment of
antecedents behaviors and consequences associated
with emotional experiences
Present-focused emotional awareness
2 1ndash3 Generalized emotion exposures practice of non-
judgmental awareness
Present-focused awareness preventing
emotional avoidance acceptance of emotion-
related physiological sensations3 1ndash3 Identifying thinking traps detective thinking skills
generating alternative thoughts problem-solving skills
Enhancing cognitive 1047298exibility
4 4+ Interoceptive exposures in-vivo exposures behavioral
activation
Preventing emotional avoidance acceptance of
physiological sensations facilitating exposure to
interoceptive and in-vivo emotional triggers
5 1ndash2 Skill consolidation relapse prevention
Optional module Suggested number of sessions Techniquesskills
1 As needed Motivational enhancement
2 0ndash3 Safety planning crisis management
3 0ndash3 (at least 1 recommended) Parenting skills
516 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 711
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 2: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/2.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 211
depressive disorders (Brown Chorpita amp Barlow 1998 Trosper
Whitton Brown amp Pincus 2012)
Youth anxiety and depressive disorders also demonstrate
similar responses to pharmacological and psychosocial interven-
tions For instance both anxiety and depression are responsive to
selective serotonin reuptake inhibitor (SSRI) medications (eg
Treatment for Adolescents with Depression Study (TADS) Team
2004 Walkup et al 2008) Prior work with cognitive-behavioral
therapy (CBT) trials have found ldquospill-overrdquo effects onto comorbid
anxiety or depressive disorders regardless of the principal
disorder For example anxiety-focused CBT has demonstrated
positive effects on comorbid depressive symptoms (Kendall
Safford Flannery-Schroeder amp Webb 2004) and a meta-analysis
of CBT for youth depression found effect sizes in anxiety symptom
reduction (ES = 039) that were only slightly less than those for
depressive symptom improvement (ES = 057 Weisz McCarty amp
Valeri 2006)
Given their frequent comorbidity shared vulnerability factors
and similar response to treatment some (eg Barlow Allen amp
Choate 2004) have advocated for a transdiagnostic or disorder-
non-speci1047297c treatment approach that targets higher-order psy-
chological factors common to the emotional disorders Such an
approach is hypothesized to allow for greater clinical
1047298exibility and
use with patients presenting with multiple emotional disorders aswell as reduce clinician burden in learning multiple disorder-
speci1047297c treatment manuals (McHugh amp Barlow 2010) As such
recent clinical research has focused upon the development and
evaluation of transdiagnostic treatments that may effectively
target anxiety and depressive disorders within a single protocol
The Uni1047297ed Protocol for the Treatment of Emotional Disorders
in Adolescence (UP-A Ehrenreich et al 2008) is a developmental
adaptation of the adult Uni1047297ed Protocol (UP Barlow et al 2010)
designed for adolescents ages 12ndash17 years old presenting with any
primary anxiety disorder unipolar depressive disorder or their
combination The UP-A has theoretical roots in emotion regulation
cognitive science and behavior modi1047297cation and distills common
evidence-based
techniques
that
cut
across
disorder-speci1047297c
treatment manuals for youth anxiety and depression (egpsychoeducation non-judgmental awareness cognitive reapprais-
al exposure behavioral activation etc) within a singular protocol
The
UP-A
incorporates
standard
evidence-based
principles
within
the
broader
function
context
and
regulation
of
a
range
of
positive
and negative emotions (eg sadness anger fear) Therefore it is
theorized to positively affect how adolescents attend to modulate
and
experience
emotions
that
cut
across
speci1047297c
disorders
Similar
to
the
UP
the
UP-A
targets
1047297ve
higher-order
principles
thought
to
be latent constructs underlying lower-order speci1047297c anxiety and
depressive disorders (1) increase present-focused awareness of
emotions
(2)
enhance
cognitive
1047298exibility
(3)
prevent
emotional
avoidance
and
maladaptive
emotion-driven
behaviors
(4)
increase
acceptance of uncomfortable emotion-related physiological sen-
sations
and
(5)
facilitate
exposure
to
bodily
and
environmentaltriggers
of
emotional
experiences
(Barlow
et
al
2010)
A prior
open
trial
of
the
UP-A
established
initial
ef 1047297cacy
with
subjects demonstrating signi1047297cant pre-post reductions in clini-
cian-rated diagnostic severity across anxiety and depressive
disorder
diagnoses
(Trosper
Buzzella
Bennett
amp
Ehrenreich
2009)
and
an
immediate
treatment
(TX)
condition
of
the
UP-A
has found to outperform an 8-week treatment-delayed waitlist
(WL) condition in clinician-rated diagnostic severity for the
principal
disorder
in
a
recently
completed
randomized
controlled
trial
(RCT
Ehrenreich-May
Queen
Rodriguez
amp
Rosen1047297eld
2012)
Analyses from this RCT also found that the presence of a depressive
disorder did not moderate treatment outcomes in the UP-A
(Ehrenreich-May
et
al
2012)
whereas
many
previous
CBT
trials
for
youth
anxiety
have
found
poorer
outcomes
for
patients
with
comorbid depression (eg Berman Weems Silverman amp Kurtines
2000 Ginsburg et al 2011 OrsquoNeil amp Kendall 2012)
To summarize youth anxiety and depression are known to
commonly co-occur with one another share multiple vulnerability
factors and may be effectively treated with a uni1047297ed treatment
approach However despite their similarities anxiety and depres-
sion have also shown to be distinct constructs For instance factor
analytic studies with school-based (Crowley amp Emerson 1996) and
clinical samples (Stavrakaki Vargo Boodoosingh amp Roberts 1987)
have found stronger support for two-factor models of anxiety and
depression compared to single factor models In addition while
both anxiety and depression are characterized by high negative
affect low positive affect has shown stronger associations with
depressive symptoms than with anxiety symptoms (for more
comprehensive reviews see Anderson amp Hope 2008 De Bolle amp De
Fruyt 2010) Given these important differences a next step in
investigating transdiagnostic treatment approaches is to examine
the separate trajectories of symptom change for anxiety and
depression over the course of treatment in order to assess if they
show similar or differential rates of change
The present study examined the separate trajectories of anxiety
and depressive symptoms over the course of the UP-A and up to
six months following the end of treatment for adolescent subjects
completing the UP-A as part of the open trial or RCT investigationWe used piecewise latent growth curve modeling (LGCM) to model
these trajectories over two separate time periods during the
course of treatment (ldquotreatment sloperdquo) and up to six months after
treatment ended (ldquofollow-up sloperdquo) Piecewise LGCM is often
recommended when examining change during treatment and
follow-up given likely non-linear change (Brown 2004) Separate
models were conducted for anxiety and depressive symptoms
Separate models were also conducted for self-rated and parent-
rated symptoms in order to examine informant differences in
symptom change trajectories Therefore a total of four piecewise
LGCMs were conducted
2
Method
21 Participants
Participants
were
59
adolescents
(576
female)
ages
12ndash17
years
old
(M
=
1542
SD
=
171)
who
received
at
least
eight
sessions
of the UP-A and completed at least one post-baseline assessment
Given the aim of the study was to examine separate trajectories of
anxiety
and
depression
symptom
change
for
those
completing
the
intervention
we
decided
to
restrict
analyses
to
those
receiving
at
least 8 sessions as this represented the minimum dosage possible
to be considered a treatment completer This subsample of 59
participants
was
culled
from
a
total
sample
of
67
participants
who
were
enrolled
in
either
the
open
trial
or
RCT
investigation
of
the
UP-A Eight (1194) of the 67 participants that did not complete at
least
eight
sessions
of
the
intervention
were
part
of
the
open
trial(n
=
2)
or
RCT
(n
=
6)
respectively
and
did
not
have
any
post-
baseline
assessment
data
T -test
and
chi-square
analyses
revealed
that those completing at least eight sessions (n = 59) did not
signi1047297cantly differ from those who dropped out prior to eight
sessions
(n
=
8)
with
regard
to
age
gender
ethnicity
severity
of
principal
diagnosis
depressive
disorder
comorbidity
status
or
baseline levels of anxiety or depressive symptoms (child or parent
report)
Participants
were
evenly
divided
between
HispanicLatino
(n
=
26
441)
and
White
Non-Hispanic
ethnicities
(n
=
26
441) The remaining subjects identi1047297ed themselves as having
BlackAfrican-American (n = 2 34) Asian-American (n = 1 17)
and
ldquootherrdquo ethnicity
(n
=
4
68)
The
median
reported
annual
family
income
was
$100000
(SD
=
$80000)
The
majority
of
512 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 311
participants had parents who were married (n = 40 678)
Remaining participants had parents who were separateddivorced
(n = 13 2203) widowed (n = 2 34) or never married (n = 4
678)
Eligibility requirements for both the open trial and RCT
included being between 12 and 17 years old (participants could
be 18 if they were still in high school) and having a primary
diagnosis of any DSM-IV anxiety andor unipolar depressive
disorder Adolescents with other psychiatric dif 1047297culties including
attention-de1047297cithyperactivity disorder (ADHD) eating disorders
and non-treatment-interfering substance abuse were eligible for
participation However the primary diagnosis had to be an anxiety
or depressive disorder Exclusion criteria included bipolar disorder
treatment-interfering substance abuse severe suicidal ideation or
recent psychiatric hospitalization treatment-interfering cognitive
functioning (eg IQ below 80) and a prior course of CBT for anxiety
or depression Participants and at least one parent were also
required to read and comprehend English well enough to complete
study measures Those concurrently receiving psychiatric medica-
tion were required to have been on a stable dosage of an SSRI
medication for three months andor a stable dosage of benzodiaz-
epine medication for one month prior to study enrollment
Adolescents completing the UP-A as part of the open trial
participated at a university-based clinic in a large urban area in theNortheastern United States (n = 15) while those in a subsequent
RCT participated at a university-based clinic in a large urban area in
the Southeastern United States (n = 44) There were no signi1047297cant
site differences with regard to gender depressive disorder
comorbidity treatment length or severity of anxiety and depres-
sive symptoms However subjects in the RCT were slightly older
(M = 1569 SD = 170) than open trial participants (M
= 1463
SD = 155) t (57) = 213 p = 004 d = 064 In addition as expected
based upon demographic characteristics of the surrounding
communities RCT participants were more likely to be Hispanic
Latino (6136) whereas all of the open trial participants were
White Non-Hispanic x2 (3) = 2553 p lt 0001 There were no
differences
among
ethnicities
with
regard
to
any
study
variables
at
any time pointsPrincipalco-principal diagnoses and comorbid diagnoses at
baseline are displayed in Table 1 (Diagnoses assigned as co-
principal
are
included
for
totals
within
the
principal
diagnosis
category)
The
most
common
principal
diagnoses
were
generalized
anxiety disorder (n = 23 3898) followed by social phobia (n= 19
3220) and major depressive disorder (n = 11 1864) Sixteen
participants (2712) were assigned co-principal diagnoses with
the most common combination being generalized anxiety disorder
and social phobia (n = 4) All of the DSM-IV anxiety disorders were
represented with either a principalco-principal or comorbid
diagnosis including obsessive-compulsive disorder (n = 8 1356)
panic disorder (n = 7 1186) speci1047297c phobia (n = 8 1356)
separation anxiety disorder (n = 2 339) and post-traumatic
stress disorder (n = 1 169)
The great majority of participants (n = 47 797) were assigned
a primary anxiety disorder diagnosis while nine participants
(153) received a primary depressive disorder diagnosis and three
participants (51) were assigned co-principal anxiety and
depressive disorder diagnoses Although only 12 participants
(2034) received a principal or co-principal depressive disorder
diagnosis comorbid depression was well-represented with 23
participants (3898) assigned a secondary comorbid depressive
disorder Therefore the majority of participants (n = 35 6102)
were assigned a depressive disorder The majority of those with a
depressive disorder were diagnosed with major depressive
disorder (n = 25) although dysthymic disorder (n = 5) and depres-
sive disorder not otherwise speci1047297ed (NOS
n = 6) were also
present (One participant was diagnosed with both major
depressive disorder and dysthymic disorder) In addition toanxiety and depression comorbidity other psychiatric conditions
were also present including ADHD (n = 4 678) oppositional-
de1047297ant disorder (n = 1 169) and eating disorder NOS (n = 1
169) No participants were assigned a diagnosis of a current
substance abuse disorder
The majority of participants (n = 46 78) were not currently
taking psychiatric medication at the time of the study Seven
participants (1186) were taking a SSRI medication alone one
participant (169) was taking benzodiazepine alone and two
participants (339) were taking both an SSRI and benzodiaze-
pine With regard to stimulant medication for ADHD symptoms
two participants (339) were taking a stimulant medication
alone
while
one
participant
(169)
was
taking
a
stimulant
medication in combination with an SSRI medication Analyses of those taking medication (n = 13) compared to those not taking
medication (n = 46) revealed no signi1047297cant differences on any
baseline
variables
In
addition
medication
status
was unrelated
to
anxiety
or
depressive
symptom
severity
during
treatment
or
at
follow-up
Table 1
Frequencies of diagnoses at baseline
Diagnosis Principal diagnosis ()a Comorbid diagnoses () Total ()
Generalized anxiety disorder 23 (3898) 15 (2542) 38 (6441)
Social phobia 19 (3220) 7 (1186) 26 (4407)
Major depressive disorder 11 (1864) 14 (2373) 25 (4237)
Obsessive-compulsive disorder 4 (678) 4 (678) 8 (1356)
Panic disorder with agoraphobia 3 (508) 3 (508)
Speci1047297c phobia 3 (508) 5 (847) 8 (1356)
Panic disorder without agoraphobia 2 (339) 2 (339) 4 (678)
Tic disorder 1 (169) 1 (169)
Anxiety disorder NOS 5 (847) 2 (339) 7 (1186)
Dysthymic disorder 2 (339) 3 (508) 5 (847)
Trichotillomania 1 (169) 1 (169)
ADHD combined type 1 (169) 2 (339) 3 (508)
Separation anxiety disorder 2 (339) 2 (339)
Depressive disorder NOS 6 (1017) 6 (1017)
Post-traumatic stress disorder 1 (169) 1 (169)
Enuresis 1 (169) 1 (169)
ADHD inattentive type 1 (169) 1 (169)
Oppositional-de1047297ant disorder 1 (169) 1 (169)
Eating disorder NOS 1 (169) 1 (169)
a Percentages do not add to 100 because some subjects had co-principal diagnoses
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 513
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 411
22 Procedure
The Institutional Review Boards of the two universities
participating in this trial granted approval for the study
Adolescents were referred for evaluation and treatment services
at the clinics by school personnel pediatricians psychiatrists
other mental health care professionals community agencies or
were self-referred through community online or radio advertise-
ments Upon contacting the clinic the adolescentrsquos parent
completed an initial telephone screen to assess primary concerns
and rule out exclusionary criteria If the primary concern was
determined to be anxiety or mood related the adolescent and
parent were scheduled for an in-person diagnostic evaluation at
the clinic Parents of adolescents not deemed eligible were
provided with appropriate treatment referrals
Fig 1 displays the CONSORT diagram outlining participant
recruitment and assignment At the initial diagnostic evaluation
the adolescent and parent separately completed the Anxiety
Disorders Interview Schedule for the DSM-IV Child Version Parent
and Child Reports (ADIS-IV-CP Silverman amp Albano 1996) with a
PhD-level clinical psychologist or doctoral student in clinical child
psychology In addition the adolescent and parent completed
paper-and-pencil questionnaires at this evaluation After obtaining
both parental consent and adolescent assent the adolescentparticipated in the ADIS-IV while the parent completed measures
in the waiting room Similarly the adolescent completed their
measures while the parent completed their interview Symptom
data collected at this initial diagnostic evaluation were used as
Time 1 data for subjects in the open trial and for those in the TX
condition in the RCT
Following the diagnostic evaluation clinician-rated composite
diagnoses were assigned by compiling information from adoles-
cent and parent responses to ADIS-IV-CP The assessor assigned a
clinical severity rating (CSR) value an indicator of diagnostic
severity and impairment to every composite diagnosis CSR values
can range from 0 to 8 with values 4 indicating clinical levels of
impairment
Only
participants
receiving
a
primary
diagnosis
of
an
anxiety or depressive disorder assigned a CSR 4 were eligible toparticipate in UP-A trial Final diagnoses and CSR values were
con1047297rmed at a weekly supervision meeting On average partic-
ipants
presented
with
moderately
severe
impairment
with
regard
to
their
primary
anxiety
or
depressive
disorder
diagnosis
(M
=
581
SD = 078 range = 4ndash7)
Adolescents assigned a primary diagnosis of an anxiety or
depressive
disorder
and who
did not
meet exclusion
criteria
were
eligible
to
enroll
in
treatment
trial Upon
obtaining
written
parental consent and adolescent assent participants in the RCT
were randomized to either the TX or the WL condition
Participants
in
the
open trial
and
TX
arm
of
the
RCT
began
treatment
immediately
All
participants and
their parent
com-
pleted symptom measures at Time 2 (8 weeks after beginning
treatment
considered
the ldquomid-treatment
rdquo
point for most)
Time3
(end
of
treatment) Time 4
(three
months after
treatment
termination)
and
Time 5
(six
months after
treatment
termina-
tion)
Participants in the WL condition did not receive treatment
during
the
8-week
WL period
but
did
brief
telephone
ldquocheck-insrdquo
with
their
assigned
therapist
to
assess
for
clinical
deterioration
every other week At the end of the WL period participants and
their parent completed symptom measures at the clinic These data
were
used
as
Time
1
data
for
WL
participants
Analyses
revealed
no
signi1047297cant
changes
in
WL participantsrsquo
data
from
initial
diagnostic
evaluation to the end of the WL period on symptom measures all
prsquos gt 020 Participants in the WL arm then began UP-A and
completed
assessments
at
same
intervals
as
those
in
the
open
trial
and
TX
arm
of
RCT
221 Treatment structure and content
The UP-A follows a principle-based
1047298exible treatment struc-
ture The intervention can be delivered over a varying length of
time (between 8 and 21 weekly sessions administered in an
individual format) There are 1047297ve required modules which
correspond to the
1047297ve core principles underlining the UPUP-A
(Barlow et al 2010) Therapists are allowed to devote more
sessions to a required module dependent upon patient needs but
ideally all modules are completed during the course of treatment
Therefore while treatment length may differ among patients all
subjects receive the same
1047297ve core modules and relevant skills
(eg psychoeducation non-judgmental awarenessmindfulness
cognitive reappraisal exposure behavioral activation) See Table 2
for a display of the
1047297ve required modules and suggested session
length for each module including treatment skills delivered within
each module and the corresponding UPUP-A core principles
targeted Importantly one of the unique features of the UP models
is the ability to target emotion regulation de1047297cits across a broader
range of positive and negative emotions compared to traditional
disorder-speci1047297c treatment manuals
In addition to the 1047297verequired modules three optional modules
are available to the therapist as needed to address parenting skills
motivational enhancement and clinical deterioration and can be
used at any point in treatment At least one parent is required to beactively involved in treatment While some variability is allowable
typically a parent is involved in the last 10ndash15min of every session
to review content and the assigned homework Individual sessions
with the parent may be used as part of an optional module if the
therapist feels that certain parenting behaviors (eg overprotec-
tion high criticism parentndashteen con1047298ict etc) are counterproduc-
tive to treatment progress or as needed for exposure planning
Motivational interviewing (Miller amp Rollnick 2002) techniques can
be used in sessions as part of a second optional module for
adolescents who appear reluctant to engage in treatment Finally
sessions within the third optional module can be used to develop a
safety plan with the adolescent and his or her parent in the event
the
patient
experiences
impulses
for
self-harm
However
adoles-
cents who show immediate risk for suicide or other pronouncedclinical deterioration could also be discontinued from UP-A studies
and referred for more intensive services if appropriate
23
Measures
231 Anxiety Disorders Interview Schedule for DSM-IV-childparent
version
(ADIS-IV-CP
Silverman
amp
Albano
1996)
The
ADIS-IV-CP
was
completed
at
the
adolescentrsquos
baseline
assessment to determine diagnostic eligibility The ADIS-IV-CP is a
semi-structured diagnostic interview for children and adolescents
ages
7ndash17years
that
assesses
all
DSM-IV
anxiety
disorders
The
ADIS-
IV-CP
also
assesses
for
unipolar
depressive
disorders
and
external-
izing disorders (ie ADHD oppositional-de1047297ant disorder conduct
disorder)
and
screens
for
substance
abuse
schizophrenia
pervasivedevelopmental
disorders
eating
disorders
and
somatoform
dis-
orders
In
addition
participants
were screened
for
bipolar
disorder
Inter-rater reliability for the primary diagnosis within this sample
was very good (k= 82 p lt 0001) All assessors were previously
trained
in
ADIS-IV-CP
administration
and
participated
in
weekly
supervision
meetings
led
by
the
third
author
(JEM)
After
an
initial
training workshop new examiners were required to reach
agreement on all clinical diagnoses and CSR levels (ie within 1
CSR
value)
with
an
expert
rater
(JEM)
on
three
consecutive
assessments
before
conducting
interviews
independently
232 Revised Childrenrsquo s Anxiety and Depression Scale
Subjects
completed
the
Revised
Childrenrsquos Anxiety
and
Depression
Scale
(RCADS
Chorpita
Yim
Mof 1047297tt
Umemoto
amp
514 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 511
A s s e s s e
d
f o r e l i g i b i l i t y ( n = 1 2 2 )
E x c l u d e d
o r D e c l i n e d ( n = 5 5 )
D i d n o t
m e e t
i n c l u s i o n c r i t e r i
a
S o u
g h t t r e a t m e
n t e l
s e w h e r e
O p t e d f o
r p r i
v a
t e t r e a t m e n t
D a t a
A v a i l a b l e
8 -
W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 2 0
)
3 M o n t h F o l
l o w
- U p ( n = 1 0
)
6 M o n t h F o l
l o w
- U p ( n = 1 1
)
E n r o l
l e d i n
R C T a n d r
a n d o m i z e d t o T X
( n = 2 6 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n
= 2 3
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n
= 3 )
D a t a a v a i l a b l e
8 - W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 1 5
)
3 M o n t h F o l
l o w
- U p ( n = 8 )
6 M o n t h F o l
l o w
- U p ( n = 6 )
E n r o l
l e d i n
R C T a n d r a n d o m i z e d t o
W
L
( n = 2 4 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n = 2 1
)
D i d n o t r
e c e i v e
a t l e a s t 8
s e s s
i o n s
( n = 3 )
E n
r o l
l e d ( n
= 6 7
)
E n r o l
l e d i n o p e n t
r i a l (
n = 1 7
)
R e c e i v e d
a t
l e a s t 8 s e s s
i o n s
( n = 1 5
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n = 2 )
D a t a
a v a i l a b l e
8 - W e e
k ( n
=
1 5
)
E n d o f T r e a t m e n t ( n
= 1 3
)
3 M o n t h
F o l
l o w
- U p
( n = 1 1
)
6 M o n t h
F o l
l o w
- U p
( n = 7 )
F i g
1
U P - A C O N S O R T 1047298 o w
d i a g r a m
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 515
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 611
Francis 2000) at all
1047297ve time points The RCADS is a 47-item self-
report measure of anxiety and depressive symptoms that containssix distinct subscales based upon DSM-IV criteria separation
anxiety social phobia generalized anxiety disorder obsessive-
compulsive disorder panic disorder and major depressive disor-
der Respondents are asked to indicate how much each item
describes them using never (0) sometimes (1) often (2) or always
(3) A Total Anxiety subscale score is comprised of 37 items and
summed from responses to the
1047297ve anxiety subscales A major
depressive disorder (MDD) subscale score is comprised of 10 items
Raw
scores
were
converted
to
T -scores
using
child
age
and
gender
to place the two subscales on the same metric with
T-scores of 65
or greater indicating borderline levels of clinical severity and T-
scores of 70 and above representing clinically signi1047297cant elevations
(Weiss
amp
Chorpita
2011)
Internal
consistency
values
for
the
RCADS
Total Anxiety subscale were as follows a= 094 at Time 1 a= 095at Time 2 a= 091 at Time 3 a= 087 at Time 4 and a= 093 at Time
5 Internal consistency values for RCADS MDD subscale were as
follows
a=
085
at
Time
1 a=
090
at
Time
2
a=
091
at
Time
3
a=
091
at
Time
4
and a=
093
at
Time
5
233 Revised childrenrsquo s anxiety and depression scales ndash parent
version
The
adolescentrsquos parent
completed
the
Revised
Childrenrsquos
Anxiety and Depression Scales-Parent version (RCADS-P Ebesu-
tani Bernstein Nakamura Chorpita amp Weisz 2010) at all 1047297ve time
points
The
RCADS-P
is
a
47-item
parent-rated
measure
of
their
childadolescentrsquos
anxiety
and
depressive
symptoms
The
RCADS-P
contains the same six subscales as the RCADS and has previously
shown
good
psychometric
properties
with
school-based
(Ebesu-tani
et
al
2011)
and
clinical
samples
(Ebesutani
et
al
2010) For
the
current
sample
internal
consistency
values
for
RCADS-P
Total
Anxiety subscale were as follows a= 092 at Time 1 a= 091 at
Time 2 a= 094 at Time 3 a= 078 at Time 4 and a= 088 at Time 5
Internal
consistency
values
for
the
RCADS-P
MDD
subscale
were
as
follows
a=
078
at
Time
1
a=
088
at
Time
2
a=
091
at
Time
3
a= 060 at Time 4 and a= 092 at Time 5
24
Data
analytic
plan
For the present study we used piecewise LGCM to model
symptom trajectories over (1) the course of treatment and (2)
during the
six-month
follow-up
period
Several
indices
of
model
1047297t
were
used
including
chi square
comparative 1047297x index
(CFI)
root mean square error of approximation (RMSEA) and stan-
dardized root mean square residual (SRMR) For purposes of interpretation indices of good model 1047297t include a non-signi1047297cant
chi square ( p gt 005) CFI gt 095 RMSEA
lt 006 and SRMR lt 008
(Kline 2011) Signi1047297cant tests for parameter estimates were
conducted with the z -statistic using a two-tailed test LGCM
analyses were conducted using MPLUS Fifth version (Muthen amp
Muthen 2005)
3 Results
The data were
1047297rst screened for normality and to determine if
there were any statistical outliers Skewness and kurtosis levels
were within acceptable ranges (Kline 2011) No signi1047297cant
outliers ( z
3)
were
identi1047297ed
at
any
time
points
All
subjects
had complete data for Time 1 as well as at least one other post-baseline assessment Fifty-1047297ve subjects (9322) had data at the 8-
week assessment (Time 2) and 48 participants (8136) had data at
the
end
of
treatment
(M
=
1558
sessions)
assessment
(Time
3)
However
there
was
considerable
missing
data
at
the
two
follow-
up time points with 29 subjects (4915) having available data
three months after treatment (Time 4) and 24 participants
(4068)
having
data
six
months
after
treatment
(Time
5)
although
6271
of
subjects
had
available
data
for
at
least
one
follow-up time point Attrition analyses revealed no signi1047297cant
differences between those with complete data and those with
missing
data
on
any
indicators
of
symptom
severity
at
baseline
or
any
demographic
variables
(eg
age
gender
ethnicity)
Further-
more those with and without follow-up data did not show
signi1047297cant
differences
on
any
variables
at
the
post-treatmentassessment
31 Descriptive statistics
See
Table
3
for
observed
means
and
standard
deviations
of
RCADSRCADS-P
Total
Anxiety
T -scores
and
RCADSRCADS-P
MDD
T -scores at each time point In addition the percentage of
participants with T -scores 65 and T -scores 70 are presented
Mean
T -scores
on
all
four
measures
reduced
to
below
65
by
Time
3
indicating
that
mean
levels
of
both
self-rated
and
parent-rated
anxiety and depressive symptoms were within the normative
range by the end of treatment Analysis of percentages of
participants
with
T -scores
65
and
T -scores
70
also
revealed
reductions
in
those
with
borderline
elevated
and
clinically
elevated
Table 2
UP-A structure and content
Required
module
Suggested
number of
sessions
Techniquesskills Core UPUP-A principle(s) targeted
1 1ndash3 Psychoeducation of emotions functional assessment of
antecedents behaviors and consequences associated
with emotional experiences
Present-focused emotional awareness
2 1ndash3 Generalized emotion exposures practice of non-
judgmental awareness
Present-focused awareness preventing
emotional avoidance acceptance of emotion-
related physiological sensations3 1ndash3 Identifying thinking traps detective thinking skills
generating alternative thoughts problem-solving skills
Enhancing cognitive 1047298exibility
4 4+ Interoceptive exposures in-vivo exposures behavioral
activation
Preventing emotional avoidance acceptance of
physiological sensations facilitating exposure to
interoceptive and in-vivo emotional triggers
5 1ndash2 Skill consolidation relapse prevention
Optional module Suggested number of sessions Techniquesskills
1 As needed Motivational enhancement
2 0ndash3 Safety planning crisis management
3 0ndash3 (at least 1 recommended) Parenting skills
516 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 711
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
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7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 311
participants had parents who were married (n = 40 678)
Remaining participants had parents who were separateddivorced
(n = 13 2203) widowed (n = 2 34) or never married (n = 4
678)
Eligibility requirements for both the open trial and RCT
included being between 12 and 17 years old (participants could
be 18 if they were still in high school) and having a primary
diagnosis of any DSM-IV anxiety andor unipolar depressive
disorder Adolescents with other psychiatric dif 1047297culties including
attention-de1047297cithyperactivity disorder (ADHD) eating disorders
and non-treatment-interfering substance abuse were eligible for
participation However the primary diagnosis had to be an anxiety
or depressive disorder Exclusion criteria included bipolar disorder
treatment-interfering substance abuse severe suicidal ideation or
recent psychiatric hospitalization treatment-interfering cognitive
functioning (eg IQ below 80) and a prior course of CBT for anxiety
or depression Participants and at least one parent were also
required to read and comprehend English well enough to complete
study measures Those concurrently receiving psychiatric medica-
tion were required to have been on a stable dosage of an SSRI
medication for three months andor a stable dosage of benzodiaz-
epine medication for one month prior to study enrollment
Adolescents completing the UP-A as part of the open trial
participated at a university-based clinic in a large urban area in theNortheastern United States (n = 15) while those in a subsequent
RCT participated at a university-based clinic in a large urban area in
the Southeastern United States (n = 44) There were no signi1047297cant
site differences with regard to gender depressive disorder
comorbidity treatment length or severity of anxiety and depres-
sive symptoms However subjects in the RCT were slightly older
(M = 1569 SD = 170) than open trial participants (M
= 1463
SD = 155) t (57) = 213 p = 004 d = 064 In addition as expected
based upon demographic characteristics of the surrounding
communities RCT participants were more likely to be Hispanic
Latino (6136) whereas all of the open trial participants were
White Non-Hispanic x2 (3) = 2553 p lt 0001 There were no
differences
among
ethnicities
with
regard
to
any
study
variables
at
any time pointsPrincipalco-principal diagnoses and comorbid diagnoses at
baseline are displayed in Table 1 (Diagnoses assigned as co-
principal
are
included
for
totals
within
the
principal
diagnosis
category)
The
most
common
principal
diagnoses
were
generalized
anxiety disorder (n = 23 3898) followed by social phobia (n= 19
3220) and major depressive disorder (n = 11 1864) Sixteen
participants (2712) were assigned co-principal diagnoses with
the most common combination being generalized anxiety disorder
and social phobia (n = 4) All of the DSM-IV anxiety disorders were
represented with either a principalco-principal or comorbid
diagnosis including obsessive-compulsive disorder (n = 8 1356)
panic disorder (n = 7 1186) speci1047297c phobia (n = 8 1356)
separation anxiety disorder (n = 2 339) and post-traumatic
stress disorder (n = 1 169)
The great majority of participants (n = 47 797) were assigned
a primary anxiety disorder diagnosis while nine participants
(153) received a primary depressive disorder diagnosis and three
participants (51) were assigned co-principal anxiety and
depressive disorder diagnoses Although only 12 participants
(2034) received a principal or co-principal depressive disorder
diagnosis comorbid depression was well-represented with 23
participants (3898) assigned a secondary comorbid depressive
disorder Therefore the majority of participants (n = 35 6102)
were assigned a depressive disorder The majority of those with a
depressive disorder were diagnosed with major depressive
disorder (n = 25) although dysthymic disorder (n = 5) and depres-
sive disorder not otherwise speci1047297ed (NOS
n = 6) were also
present (One participant was diagnosed with both major
depressive disorder and dysthymic disorder) In addition toanxiety and depression comorbidity other psychiatric conditions
were also present including ADHD (n = 4 678) oppositional-
de1047297ant disorder (n = 1 169) and eating disorder NOS (n = 1
169) No participants were assigned a diagnosis of a current
substance abuse disorder
The majority of participants (n = 46 78) were not currently
taking psychiatric medication at the time of the study Seven
participants (1186) were taking a SSRI medication alone one
participant (169) was taking benzodiazepine alone and two
participants (339) were taking both an SSRI and benzodiaze-
pine With regard to stimulant medication for ADHD symptoms
two participants (339) were taking a stimulant medication
alone
while
one
participant
(169)
was
taking
a
stimulant
medication in combination with an SSRI medication Analyses of those taking medication (n = 13) compared to those not taking
medication (n = 46) revealed no signi1047297cant differences on any
baseline
variables
In
addition
medication
status
was unrelated
to
anxiety
or
depressive
symptom
severity
during
treatment
or
at
follow-up
Table 1
Frequencies of diagnoses at baseline
Diagnosis Principal diagnosis ()a Comorbid diagnoses () Total ()
Generalized anxiety disorder 23 (3898) 15 (2542) 38 (6441)
Social phobia 19 (3220) 7 (1186) 26 (4407)
Major depressive disorder 11 (1864) 14 (2373) 25 (4237)
Obsessive-compulsive disorder 4 (678) 4 (678) 8 (1356)
Panic disorder with agoraphobia 3 (508) 3 (508)
Speci1047297c phobia 3 (508) 5 (847) 8 (1356)
Panic disorder without agoraphobia 2 (339) 2 (339) 4 (678)
Tic disorder 1 (169) 1 (169)
Anxiety disorder NOS 5 (847) 2 (339) 7 (1186)
Dysthymic disorder 2 (339) 3 (508) 5 (847)
Trichotillomania 1 (169) 1 (169)
ADHD combined type 1 (169) 2 (339) 3 (508)
Separation anxiety disorder 2 (339) 2 (339)
Depressive disorder NOS 6 (1017) 6 (1017)
Post-traumatic stress disorder 1 (169) 1 (169)
Enuresis 1 (169) 1 (169)
ADHD inattentive type 1 (169) 1 (169)
Oppositional-de1047297ant disorder 1 (169) 1 (169)
Eating disorder NOS 1 (169) 1 (169)
a Percentages do not add to 100 because some subjects had co-principal diagnoses
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 513
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 411
22 Procedure
The Institutional Review Boards of the two universities
participating in this trial granted approval for the study
Adolescents were referred for evaluation and treatment services
at the clinics by school personnel pediatricians psychiatrists
other mental health care professionals community agencies or
were self-referred through community online or radio advertise-
ments Upon contacting the clinic the adolescentrsquos parent
completed an initial telephone screen to assess primary concerns
and rule out exclusionary criteria If the primary concern was
determined to be anxiety or mood related the adolescent and
parent were scheduled for an in-person diagnostic evaluation at
the clinic Parents of adolescents not deemed eligible were
provided with appropriate treatment referrals
Fig 1 displays the CONSORT diagram outlining participant
recruitment and assignment At the initial diagnostic evaluation
the adolescent and parent separately completed the Anxiety
Disorders Interview Schedule for the DSM-IV Child Version Parent
and Child Reports (ADIS-IV-CP Silverman amp Albano 1996) with a
PhD-level clinical psychologist or doctoral student in clinical child
psychology In addition the adolescent and parent completed
paper-and-pencil questionnaires at this evaluation After obtaining
both parental consent and adolescent assent the adolescentparticipated in the ADIS-IV while the parent completed measures
in the waiting room Similarly the adolescent completed their
measures while the parent completed their interview Symptom
data collected at this initial diagnostic evaluation were used as
Time 1 data for subjects in the open trial and for those in the TX
condition in the RCT
Following the diagnostic evaluation clinician-rated composite
diagnoses were assigned by compiling information from adoles-
cent and parent responses to ADIS-IV-CP The assessor assigned a
clinical severity rating (CSR) value an indicator of diagnostic
severity and impairment to every composite diagnosis CSR values
can range from 0 to 8 with values 4 indicating clinical levels of
impairment
Only
participants
receiving
a
primary
diagnosis
of
an
anxiety or depressive disorder assigned a CSR 4 were eligible toparticipate in UP-A trial Final diagnoses and CSR values were
con1047297rmed at a weekly supervision meeting On average partic-
ipants
presented
with
moderately
severe
impairment
with
regard
to
their
primary
anxiety
or
depressive
disorder
diagnosis
(M
=
581
SD = 078 range = 4ndash7)
Adolescents assigned a primary diagnosis of an anxiety or
depressive
disorder
and who
did not
meet exclusion
criteria
were
eligible
to
enroll
in
treatment
trial Upon
obtaining
written
parental consent and adolescent assent participants in the RCT
were randomized to either the TX or the WL condition
Participants
in
the
open trial
and
TX
arm
of
the
RCT
began
treatment
immediately
All
participants and
their parent
com-
pleted symptom measures at Time 2 (8 weeks after beginning
treatment
considered
the ldquomid-treatment
rdquo
point for most)
Time3
(end
of
treatment) Time 4
(three
months after
treatment
termination)
and
Time 5
(six
months after
treatment
termina-
tion)
Participants in the WL condition did not receive treatment
during
the
8-week
WL period
but
did
brief
telephone
ldquocheck-insrdquo
with
their
assigned
therapist
to
assess
for
clinical
deterioration
every other week At the end of the WL period participants and
their parent completed symptom measures at the clinic These data
were
used
as
Time
1
data
for
WL
participants
Analyses
revealed
no
signi1047297cant
changes
in
WL participantsrsquo
data
from
initial
diagnostic
evaluation to the end of the WL period on symptom measures all
prsquos gt 020 Participants in the WL arm then began UP-A and
completed
assessments
at
same
intervals
as
those
in
the
open
trial
and
TX
arm
of
RCT
221 Treatment structure and content
The UP-A follows a principle-based
1047298exible treatment struc-
ture The intervention can be delivered over a varying length of
time (between 8 and 21 weekly sessions administered in an
individual format) There are 1047297ve required modules which
correspond to the
1047297ve core principles underlining the UPUP-A
(Barlow et al 2010) Therapists are allowed to devote more
sessions to a required module dependent upon patient needs but
ideally all modules are completed during the course of treatment
Therefore while treatment length may differ among patients all
subjects receive the same
1047297ve core modules and relevant skills
(eg psychoeducation non-judgmental awarenessmindfulness
cognitive reappraisal exposure behavioral activation) See Table 2
for a display of the
1047297ve required modules and suggested session
length for each module including treatment skills delivered within
each module and the corresponding UPUP-A core principles
targeted Importantly one of the unique features of the UP models
is the ability to target emotion regulation de1047297cits across a broader
range of positive and negative emotions compared to traditional
disorder-speci1047297c treatment manuals
In addition to the 1047297verequired modules three optional modules
are available to the therapist as needed to address parenting skills
motivational enhancement and clinical deterioration and can be
used at any point in treatment At least one parent is required to beactively involved in treatment While some variability is allowable
typically a parent is involved in the last 10ndash15min of every session
to review content and the assigned homework Individual sessions
with the parent may be used as part of an optional module if the
therapist feels that certain parenting behaviors (eg overprotec-
tion high criticism parentndashteen con1047298ict etc) are counterproduc-
tive to treatment progress or as needed for exposure planning
Motivational interviewing (Miller amp Rollnick 2002) techniques can
be used in sessions as part of a second optional module for
adolescents who appear reluctant to engage in treatment Finally
sessions within the third optional module can be used to develop a
safety plan with the adolescent and his or her parent in the event
the
patient
experiences
impulses
for
self-harm
However
adoles-
cents who show immediate risk for suicide or other pronouncedclinical deterioration could also be discontinued from UP-A studies
and referred for more intensive services if appropriate
23
Measures
231 Anxiety Disorders Interview Schedule for DSM-IV-childparent
version
(ADIS-IV-CP
Silverman
amp
Albano
1996)
The
ADIS-IV-CP
was
completed
at
the
adolescentrsquos
baseline
assessment to determine diagnostic eligibility The ADIS-IV-CP is a
semi-structured diagnostic interview for children and adolescents
ages
7ndash17years
that
assesses
all
DSM-IV
anxiety
disorders
The
ADIS-
IV-CP
also
assesses
for
unipolar
depressive
disorders
and
external-
izing disorders (ie ADHD oppositional-de1047297ant disorder conduct
disorder)
and
screens
for
substance
abuse
schizophrenia
pervasivedevelopmental
disorders
eating
disorders
and
somatoform
dis-
orders
In
addition
participants
were screened
for
bipolar
disorder
Inter-rater reliability for the primary diagnosis within this sample
was very good (k= 82 p lt 0001) All assessors were previously
trained
in
ADIS-IV-CP
administration
and
participated
in
weekly
supervision
meetings
led
by
the
third
author
(JEM)
After
an
initial
training workshop new examiners were required to reach
agreement on all clinical diagnoses and CSR levels (ie within 1
CSR
value)
with
an
expert
rater
(JEM)
on
three
consecutive
assessments
before
conducting
interviews
independently
232 Revised Childrenrsquo s Anxiety and Depression Scale
Subjects
completed
the
Revised
Childrenrsquos Anxiety
and
Depression
Scale
(RCADS
Chorpita
Yim
Mof 1047297tt
Umemoto
amp
514 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 511
A s s e s s e
d
f o r e l i g i b i l i t y ( n = 1 2 2 )
E x c l u d e d
o r D e c l i n e d ( n = 5 5 )
D i d n o t
m e e t
i n c l u s i o n c r i t e r i
a
S o u
g h t t r e a t m e
n t e l
s e w h e r e
O p t e d f o
r p r i
v a
t e t r e a t m e n t
D a t a
A v a i l a b l e
8 -
W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 2 0
)
3 M o n t h F o l
l o w
- U p ( n = 1 0
)
6 M o n t h F o l
l o w
- U p ( n = 1 1
)
E n r o l
l e d i n
R C T a n d r
a n d o m i z e d t o T X
( n = 2 6 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n
= 2 3
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n
= 3 )
D a t a a v a i l a b l e
8 - W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 1 5
)
3 M o n t h F o l
l o w
- U p ( n = 8 )
6 M o n t h F o l
l o w
- U p ( n = 6 )
E n r o l
l e d i n
R C T a n d r a n d o m i z e d t o
W
L
( n = 2 4 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n = 2 1
)
D i d n o t r
e c e i v e
a t l e a s t 8
s e s s
i o n s
( n = 3 )
E n
r o l
l e d ( n
= 6 7
)
E n r o l
l e d i n o p e n t
r i a l (
n = 1 7
)
R e c e i v e d
a t
l e a s t 8 s e s s
i o n s
( n = 1 5
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n = 2 )
D a t a
a v a i l a b l e
8 - W e e
k ( n
=
1 5
)
E n d o f T r e a t m e n t ( n
= 1 3
)
3 M o n t h
F o l
l o w
- U p
( n = 1 1
)
6 M o n t h
F o l
l o w
- U p
( n = 7 )
F i g
1
U P - A C O N S O R T 1047298 o w
d i a g r a m
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 515
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 611
Francis 2000) at all
1047297ve time points The RCADS is a 47-item self-
report measure of anxiety and depressive symptoms that containssix distinct subscales based upon DSM-IV criteria separation
anxiety social phobia generalized anxiety disorder obsessive-
compulsive disorder panic disorder and major depressive disor-
der Respondents are asked to indicate how much each item
describes them using never (0) sometimes (1) often (2) or always
(3) A Total Anxiety subscale score is comprised of 37 items and
summed from responses to the
1047297ve anxiety subscales A major
depressive disorder (MDD) subscale score is comprised of 10 items
Raw
scores
were
converted
to
T -scores
using
child
age
and
gender
to place the two subscales on the same metric with
T-scores of 65
or greater indicating borderline levels of clinical severity and T-
scores of 70 and above representing clinically signi1047297cant elevations
(Weiss
amp
Chorpita
2011)
Internal
consistency
values
for
the
RCADS
Total Anxiety subscale were as follows a= 094 at Time 1 a= 095at Time 2 a= 091 at Time 3 a= 087 at Time 4 and a= 093 at Time
5 Internal consistency values for RCADS MDD subscale were as
follows
a=
085
at
Time
1 a=
090
at
Time
2
a=
091
at
Time
3
a=
091
at
Time
4
and a=
093
at
Time
5
233 Revised childrenrsquo s anxiety and depression scales ndash parent
version
The
adolescentrsquos parent
completed
the
Revised
Childrenrsquos
Anxiety and Depression Scales-Parent version (RCADS-P Ebesu-
tani Bernstein Nakamura Chorpita amp Weisz 2010) at all 1047297ve time
points
The
RCADS-P
is
a
47-item
parent-rated
measure
of
their
childadolescentrsquos
anxiety
and
depressive
symptoms
The
RCADS-P
contains the same six subscales as the RCADS and has previously
shown
good
psychometric
properties
with
school-based
(Ebesu-tani
et
al
2011)
and
clinical
samples
(Ebesutani
et
al
2010) For
the
current
sample
internal
consistency
values
for
RCADS-P
Total
Anxiety subscale were as follows a= 092 at Time 1 a= 091 at
Time 2 a= 094 at Time 3 a= 078 at Time 4 and a= 088 at Time 5
Internal
consistency
values
for
the
RCADS-P
MDD
subscale
were
as
follows
a=
078
at
Time
1
a=
088
at
Time
2
a=
091
at
Time
3
a= 060 at Time 4 and a= 092 at Time 5
24
Data
analytic
plan
For the present study we used piecewise LGCM to model
symptom trajectories over (1) the course of treatment and (2)
during the
six-month
follow-up
period
Several
indices
of
model
1047297t
were
used
including
chi square
comparative 1047297x index
(CFI)
root mean square error of approximation (RMSEA) and stan-
dardized root mean square residual (SRMR) For purposes of interpretation indices of good model 1047297t include a non-signi1047297cant
chi square ( p gt 005) CFI gt 095 RMSEA
lt 006 and SRMR lt 008
(Kline 2011) Signi1047297cant tests for parameter estimates were
conducted with the z -statistic using a two-tailed test LGCM
analyses were conducted using MPLUS Fifth version (Muthen amp
Muthen 2005)
3 Results
The data were
1047297rst screened for normality and to determine if
there were any statistical outliers Skewness and kurtosis levels
were within acceptable ranges (Kline 2011) No signi1047297cant
outliers ( z
3)
were
identi1047297ed
at
any
time
points
All
subjects
had complete data for Time 1 as well as at least one other post-baseline assessment Fifty-1047297ve subjects (9322) had data at the 8-
week assessment (Time 2) and 48 participants (8136) had data at
the
end
of
treatment
(M
=
1558
sessions)
assessment
(Time
3)
However
there
was
considerable
missing
data
at
the
two
follow-
up time points with 29 subjects (4915) having available data
three months after treatment (Time 4) and 24 participants
(4068)
having
data
six
months
after
treatment
(Time
5)
although
6271
of
subjects
had
available
data
for
at
least
one
follow-up time point Attrition analyses revealed no signi1047297cant
differences between those with complete data and those with
missing
data
on
any
indicators
of
symptom
severity
at
baseline
or
any
demographic
variables
(eg
age
gender
ethnicity)
Further-
more those with and without follow-up data did not show
signi1047297cant
differences
on
any
variables
at
the
post-treatmentassessment
31 Descriptive statistics
See
Table
3
for
observed
means
and
standard
deviations
of
RCADSRCADS-P
Total
Anxiety
T -scores
and
RCADSRCADS-P
MDD
T -scores at each time point In addition the percentage of
participants with T -scores 65 and T -scores 70 are presented
Mean
T -scores
on
all
four
measures
reduced
to
below
65
by
Time
3
indicating
that
mean
levels
of
both
self-rated
and
parent-rated
anxiety and depressive symptoms were within the normative
range by the end of treatment Analysis of percentages of
participants
with
T -scores
65
and
T -scores
70
also
revealed
reductions
in
those
with
borderline
elevated
and
clinically
elevated
Table 2
UP-A structure and content
Required
module
Suggested
number of
sessions
Techniquesskills Core UPUP-A principle(s) targeted
1 1ndash3 Psychoeducation of emotions functional assessment of
antecedents behaviors and consequences associated
with emotional experiences
Present-focused emotional awareness
2 1ndash3 Generalized emotion exposures practice of non-
judgmental awareness
Present-focused awareness preventing
emotional avoidance acceptance of emotion-
related physiological sensations3 1ndash3 Identifying thinking traps detective thinking skills
generating alternative thoughts problem-solving skills
Enhancing cognitive 1047298exibility
4 4+ Interoceptive exposures in-vivo exposures behavioral
activation
Preventing emotional avoidance acceptance of
physiological sensations facilitating exposure to
interoceptive and in-vivo emotional triggers
5 1ndash2 Skill consolidation relapse prevention
Optional module Suggested number of sessions Techniquesskills
1 As needed Motivational enhancement
2 0ndash3 Safety planning crisis management
3 0ndash3 (at least 1 recommended) Parenting skills
516 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 711
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 4: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/4.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 411
22 Procedure
The Institutional Review Boards of the two universities
participating in this trial granted approval for the study
Adolescents were referred for evaluation and treatment services
at the clinics by school personnel pediatricians psychiatrists
other mental health care professionals community agencies or
were self-referred through community online or radio advertise-
ments Upon contacting the clinic the adolescentrsquos parent
completed an initial telephone screen to assess primary concerns
and rule out exclusionary criteria If the primary concern was
determined to be anxiety or mood related the adolescent and
parent were scheduled for an in-person diagnostic evaluation at
the clinic Parents of adolescents not deemed eligible were
provided with appropriate treatment referrals
Fig 1 displays the CONSORT diagram outlining participant
recruitment and assignment At the initial diagnostic evaluation
the adolescent and parent separately completed the Anxiety
Disorders Interview Schedule for the DSM-IV Child Version Parent
and Child Reports (ADIS-IV-CP Silverman amp Albano 1996) with a
PhD-level clinical psychologist or doctoral student in clinical child
psychology In addition the adolescent and parent completed
paper-and-pencil questionnaires at this evaluation After obtaining
both parental consent and adolescent assent the adolescentparticipated in the ADIS-IV while the parent completed measures
in the waiting room Similarly the adolescent completed their
measures while the parent completed their interview Symptom
data collected at this initial diagnostic evaluation were used as
Time 1 data for subjects in the open trial and for those in the TX
condition in the RCT
Following the diagnostic evaluation clinician-rated composite
diagnoses were assigned by compiling information from adoles-
cent and parent responses to ADIS-IV-CP The assessor assigned a
clinical severity rating (CSR) value an indicator of diagnostic
severity and impairment to every composite diagnosis CSR values
can range from 0 to 8 with values 4 indicating clinical levels of
impairment
Only
participants
receiving
a
primary
diagnosis
of
an
anxiety or depressive disorder assigned a CSR 4 were eligible toparticipate in UP-A trial Final diagnoses and CSR values were
con1047297rmed at a weekly supervision meeting On average partic-
ipants
presented
with
moderately
severe
impairment
with
regard
to
their
primary
anxiety
or
depressive
disorder
diagnosis
(M
=
581
SD = 078 range = 4ndash7)
Adolescents assigned a primary diagnosis of an anxiety or
depressive
disorder
and who
did not
meet exclusion
criteria
were
eligible
to
enroll
in
treatment
trial Upon
obtaining
written
parental consent and adolescent assent participants in the RCT
were randomized to either the TX or the WL condition
Participants
in
the
open trial
and
TX
arm
of
the
RCT
began
treatment
immediately
All
participants and
their parent
com-
pleted symptom measures at Time 2 (8 weeks after beginning
treatment
considered
the ldquomid-treatment
rdquo
point for most)
Time3
(end
of
treatment) Time 4
(three
months after
treatment
termination)
and
Time 5
(six
months after
treatment
termina-
tion)
Participants in the WL condition did not receive treatment
during
the
8-week
WL period
but
did
brief
telephone
ldquocheck-insrdquo
with
their
assigned
therapist
to
assess
for
clinical
deterioration
every other week At the end of the WL period participants and
their parent completed symptom measures at the clinic These data
were
used
as
Time
1
data
for
WL
participants
Analyses
revealed
no
signi1047297cant
changes
in
WL participantsrsquo
data
from
initial
diagnostic
evaluation to the end of the WL period on symptom measures all
prsquos gt 020 Participants in the WL arm then began UP-A and
completed
assessments
at
same
intervals
as
those
in
the
open
trial
and
TX
arm
of
RCT
221 Treatment structure and content
The UP-A follows a principle-based
1047298exible treatment struc-
ture The intervention can be delivered over a varying length of
time (between 8 and 21 weekly sessions administered in an
individual format) There are 1047297ve required modules which
correspond to the
1047297ve core principles underlining the UPUP-A
(Barlow et al 2010) Therapists are allowed to devote more
sessions to a required module dependent upon patient needs but
ideally all modules are completed during the course of treatment
Therefore while treatment length may differ among patients all
subjects receive the same
1047297ve core modules and relevant skills
(eg psychoeducation non-judgmental awarenessmindfulness
cognitive reappraisal exposure behavioral activation) See Table 2
for a display of the
1047297ve required modules and suggested session
length for each module including treatment skills delivered within
each module and the corresponding UPUP-A core principles
targeted Importantly one of the unique features of the UP models
is the ability to target emotion regulation de1047297cits across a broader
range of positive and negative emotions compared to traditional
disorder-speci1047297c treatment manuals
In addition to the 1047297verequired modules three optional modules
are available to the therapist as needed to address parenting skills
motivational enhancement and clinical deterioration and can be
used at any point in treatment At least one parent is required to beactively involved in treatment While some variability is allowable
typically a parent is involved in the last 10ndash15min of every session
to review content and the assigned homework Individual sessions
with the parent may be used as part of an optional module if the
therapist feels that certain parenting behaviors (eg overprotec-
tion high criticism parentndashteen con1047298ict etc) are counterproduc-
tive to treatment progress or as needed for exposure planning
Motivational interviewing (Miller amp Rollnick 2002) techniques can
be used in sessions as part of a second optional module for
adolescents who appear reluctant to engage in treatment Finally
sessions within the third optional module can be used to develop a
safety plan with the adolescent and his or her parent in the event
the
patient
experiences
impulses
for
self-harm
However
adoles-
cents who show immediate risk for suicide or other pronouncedclinical deterioration could also be discontinued from UP-A studies
and referred for more intensive services if appropriate
23
Measures
231 Anxiety Disorders Interview Schedule for DSM-IV-childparent
version
(ADIS-IV-CP
Silverman
amp
Albano
1996)
The
ADIS-IV-CP
was
completed
at
the
adolescentrsquos
baseline
assessment to determine diagnostic eligibility The ADIS-IV-CP is a
semi-structured diagnostic interview for children and adolescents
ages
7ndash17years
that
assesses
all
DSM-IV
anxiety
disorders
The
ADIS-
IV-CP
also
assesses
for
unipolar
depressive
disorders
and
external-
izing disorders (ie ADHD oppositional-de1047297ant disorder conduct
disorder)
and
screens
for
substance
abuse
schizophrenia
pervasivedevelopmental
disorders
eating
disorders
and
somatoform
dis-
orders
In
addition
participants
were screened
for
bipolar
disorder
Inter-rater reliability for the primary diagnosis within this sample
was very good (k= 82 p lt 0001) All assessors were previously
trained
in
ADIS-IV-CP
administration
and
participated
in
weekly
supervision
meetings
led
by
the
third
author
(JEM)
After
an
initial
training workshop new examiners were required to reach
agreement on all clinical diagnoses and CSR levels (ie within 1
CSR
value)
with
an
expert
rater
(JEM)
on
three
consecutive
assessments
before
conducting
interviews
independently
232 Revised Childrenrsquo s Anxiety and Depression Scale
Subjects
completed
the
Revised
Childrenrsquos Anxiety
and
Depression
Scale
(RCADS
Chorpita
Yim
Mof 1047297tt
Umemoto
amp
514 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 511
A s s e s s e
d
f o r e l i g i b i l i t y ( n = 1 2 2 )
E x c l u d e d
o r D e c l i n e d ( n = 5 5 )
D i d n o t
m e e t
i n c l u s i o n c r i t e r i
a
S o u
g h t t r e a t m e
n t e l
s e w h e r e
O p t e d f o
r p r i
v a
t e t r e a t m e n t
D a t a
A v a i l a b l e
8 -
W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 2 0
)
3 M o n t h F o l
l o w
- U p ( n = 1 0
)
6 M o n t h F o l
l o w
- U p ( n = 1 1
)
E n r o l
l e d i n
R C T a n d r
a n d o m i z e d t o T X
( n = 2 6 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n
= 2 3
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n
= 3 )
D a t a a v a i l a b l e
8 - W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 1 5
)
3 M o n t h F o l
l o w
- U p ( n = 8 )
6 M o n t h F o l
l o w
- U p ( n = 6 )
E n r o l
l e d i n
R C T a n d r a n d o m i z e d t o
W
L
( n = 2 4 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n = 2 1
)
D i d n o t r
e c e i v e
a t l e a s t 8
s e s s
i o n s
( n = 3 )
E n
r o l
l e d ( n
= 6 7
)
E n r o l
l e d i n o p e n t
r i a l (
n = 1 7
)
R e c e i v e d
a t
l e a s t 8 s e s s
i o n s
( n = 1 5
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n = 2 )
D a t a
a v a i l a b l e
8 - W e e
k ( n
=
1 5
)
E n d o f T r e a t m e n t ( n
= 1 3
)
3 M o n t h
F o l
l o w
- U p
( n = 1 1
)
6 M o n t h
F o l
l o w
- U p
( n = 7 )
F i g
1
U P - A C O N S O R T 1047298 o w
d i a g r a m
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 515
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 611
Francis 2000) at all
1047297ve time points The RCADS is a 47-item self-
report measure of anxiety and depressive symptoms that containssix distinct subscales based upon DSM-IV criteria separation
anxiety social phobia generalized anxiety disorder obsessive-
compulsive disorder panic disorder and major depressive disor-
der Respondents are asked to indicate how much each item
describes them using never (0) sometimes (1) often (2) or always
(3) A Total Anxiety subscale score is comprised of 37 items and
summed from responses to the
1047297ve anxiety subscales A major
depressive disorder (MDD) subscale score is comprised of 10 items
Raw
scores
were
converted
to
T -scores
using
child
age
and
gender
to place the two subscales on the same metric with
T-scores of 65
or greater indicating borderline levels of clinical severity and T-
scores of 70 and above representing clinically signi1047297cant elevations
(Weiss
amp
Chorpita
2011)
Internal
consistency
values
for
the
RCADS
Total Anxiety subscale were as follows a= 094 at Time 1 a= 095at Time 2 a= 091 at Time 3 a= 087 at Time 4 and a= 093 at Time
5 Internal consistency values for RCADS MDD subscale were as
follows
a=
085
at
Time
1 a=
090
at
Time
2
a=
091
at
Time
3
a=
091
at
Time
4
and a=
093
at
Time
5
233 Revised childrenrsquo s anxiety and depression scales ndash parent
version
The
adolescentrsquos parent
completed
the
Revised
Childrenrsquos
Anxiety and Depression Scales-Parent version (RCADS-P Ebesu-
tani Bernstein Nakamura Chorpita amp Weisz 2010) at all 1047297ve time
points
The
RCADS-P
is
a
47-item
parent-rated
measure
of
their
childadolescentrsquos
anxiety
and
depressive
symptoms
The
RCADS-P
contains the same six subscales as the RCADS and has previously
shown
good
psychometric
properties
with
school-based
(Ebesu-tani
et
al
2011)
and
clinical
samples
(Ebesutani
et
al
2010) For
the
current
sample
internal
consistency
values
for
RCADS-P
Total
Anxiety subscale were as follows a= 092 at Time 1 a= 091 at
Time 2 a= 094 at Time 3 a= 078 at Time 4 and a= 088 at Time 5
Internal
consistency
values
for
the
RCADS-P
MDD
subscale
were
as
follows
a=
078
at
Time
1
a=
088
at
Time
2
a=
091
at
Time
3
a= 060 at Time 4 and a= 092 at Time 5
24
Data
analytic
plan
For the present study we used piecewise LGCM to model
symptom trajectories over (1) the course of treatment and (2)
during the
six-month
follow-up
period
Several
indices
of
model
1047297t
were
used
including
chi square
comparative 1047297x index
(CFI)
root mean square error of approximation (RMSEA) and stan-
dardized root mean square residual (SRMR) For purposes of interpretation indices of good model 1047297t include a non-signi1047297cant
chi square ( p gt 005) CFI gt 095 RMSEA
lt 006 and SRMR lt 008
(Kline 2011) Signi1047297cant tests for parameter estimates were
conducted with the z -statistic using a two-tailed test LGCM
analyses were conducted using MPLUS Fifth version (Muthen amp
Muthen 2005)
3 Results
The data were
1047297rst screened for normality and to determine if
there were any statistical outliers Skewness and kurtosis levels
were within acceptable ranges (Kline 2011) No signi1047297cant
outliers ( z
3)
were
identi1047297ed
at
any
time
points
All
subjects
had complete data for Time 1 as well as at least one other post-baseline assessment Fifty-1047297ve subjects (9322) had data at the 8-
week assessment (Time 2) and 48 participants (8136) had data at
the
end
of
treatment
(M
=
1558
sessions)
assessment
(Time
3)
However
there
was
considerable
missing
data
at
the
two
follow-
up time points with 29 subjects (4915) having available data
three months after treatment (Time 4) and 24 participants
(4068)
having
data
six
months
after
treatment
(Time
5)
although
6271
of
subjects
had
available
data
for
at
least
one
follow-up time point Attrition analyses revealed no signi1047297cant
differences between those with complete data and those with
missing
data
on
any
indicators
of
symptom
severity
at
baseline
or
any
demographic
variables
(eg
age
gender
ethnicity)
Further-
more those with and without follow-up data did not show
signi1047297cant
differences
on
any
variables
at
the
post-treatmentassessment
31 Descriptive statistics
See
Table
3
for
observed
means
and
standard
deviations
of
RCADSRCADS-P
Total
Anxiety
T -scores
and
RCADSRCADS-P
MDD
T -scores at each time point In addition the percentage of
participants with T -scores 65 and T -scores 70 are presented
Mean
T -scores
on
all
four
measures
reduced
to
below
65
by
Time
3
indicating
that
mean
levels
of
both
self-rated
and
parent-rated
anxiety and depressive symptoms were within the normative
range by the end of treatment Analysis of percentages of
participants
with
T -scores
65
and
T -scores
70
also
revealed
reductions
in
those
with
borderline
elevated
and
clinically
elevated
Table 2
UP-A structure and content
Required
module
Suggested
number of
sessions
Techniquesskills Core UPUP-A principle(s) targeted
1 1ndash3 Psychoeducation of emotions functional assessment of
antecedents behaviors and consequences associated
with emotional experiences
Present-focused emotional awareness
2 1ndash3 Generalized emotion exposures practice of non-
judgmental awareness
Present-focused awareness preventing
emotional avoidance acceptance of emotion-
related physiological sensations3 1ndash3 Identifying thinking traps detective thinking skills
generating alternative thoughts problem-solving skills
Enhancing cognitive 1047298exibility
4 4+ Interoceptive exposures in-vivo exposures behavioral
activation
Preventing emotional avoidance acceptance of
physiological sensations facilitating exposure to
interoceptive and in-vivo emotional triggers
5 1ndash2 Skill consolidation relapse prevention
Optional module Suggested number of sessions Techniquesskills
1 As needed Motivational enhancement
2 0ndash3 Safety planning crisis management
3 0ndash3 (at least 1 recommended) Parenting skills
516 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
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7212019 Queen 2014
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The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 5: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/5.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 511
A s s e s s e
d
f o r e l i g i b i l i t y ( n = 1 2 2 )
E x c l u d e d
o r D e c l i n e d ( n = 5 5 )
D i d n o t
m e e t
i n c l u s i o n c r i t e r i
a
S o u
g h t t r e a t m e
n t e l
s e w h e r e
O p t e d f o
r p r i
v a
t e t r e a t m e n t
D a t a
A v a i l a b l e
8 -
W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 2 0
)
3 M o n t h F o l
l o w
- U p ( n = 1 0
)
6 M o n t h F o l
l o w
- U p ( n = 1 1
)
E n r o l
l e d i n
R C T a n d r
a n d o m i z e d t o T X
( n = 2 6 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n
= 2 3
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n
= 3 )
D a t a a v a i l a b l e
8 - W e e k ( n
= 2 0
)
E n d o f T r e a t m e n t ( n
= 1 5
)
3 M o n t h F o l
l o w
- U p ( n = 8 )
6 M o n t h F o l
l o w
- U p ( n = 6 )
E n r o l
l e d i n
R C T a n d r a n d o m i z e d t o
W
L
( n = 2 4 )
R e c e
i v e d a t l e a s t 8
s e s s
i o n s
( n = 2 1
)
D i d n o t r
e c e i v e
a t l e a s t 8
s e s s
i o n s
( n = 3 )
E n
r o l
l e d ( n
= 6 7
)
E n r o l
l e d i n o p e n t
r i a l (
n = 1 7
)
R e c e i v e d
a t
l e a s t 8 s e s s
i o n s
( n = 1 5
)
D i d n o
t r e c e
i v e a t l e a s t 8
s e s s
i o n s
( n = 2 )
D a t a
a v a i l a b l e
8 - W e e
k ( n
=
1 5
)
E n d o f T r e a t m e n t ( n
= 1 3
)
3 M o n t h
F o l
l o w
- U p
( n = 1 1
)
6 M o n t h
F o l
l o w
- U p
( n = 7 )
F i g
1
U P - A C O N S O R T 1047298 o w
d i a g r a m
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 515
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 611
Francis 2000) at all
1047297ve time points The RCADS is a 47-item self-
report measure of anxiety and depressive symptoms that containssix distinct subscales based upon DSM-IV criteria separation
anxiety social phobia generalized anxiety disorder obsessive-
compulsive disorder panic disorder and major depressive disor-
der Respondents are asked to indicate how much each item
describes them using never (0) sometimes (1) often (2) or always
(3) A Total Anxiety subscale score is comprised of 37 items and
summed from responses to the
1047297ve anxiety subscales A major
depressive disorder (MDD) subscale score is comprised of 10 items
Raw
scores
were
converted
to
T -scores
using
child
age
and
gender
to place the two subscales on the same metric with
T-scores of 65
or greater indicating borderline levels of clinical severity and T-
scores of 70 and above representing clinically signi1047297cant elevations
(Weiss
amp
Chorpita
2011)
Internal
consistency
values
for
the
RCADS
Total Anxiety subscale were as follows a= 094 at Time 1 a= 095at Time 2 a= 091 at Time 3 a= 087 at Time 4 and a= 093 at Time
5 Internal consistency values for RCADS MDD subscale were as
follows
a=
085
at
Time
1 a=
090
at
Time
2
a=
091
at
Time
3
a=
091
at
Time
4
and a=
093
at
Time
5
233 Revised childrenrsquo s anxiety and depression scales ndash parent
version
The
adolescentrsquos parent
completed
the
Revised
Childrenrsquos
Anxiety and Depression Scales-Parent version (RCADS-P Ebesu-
tani Bernstein Nakamura Chorpita amp Weisz 2010) at all 1047297ve time
points
The
RCADS-P
is
a
47-item
parent-rated
measure
of
their
childadolescentrsquos
anxiety
and
depressive
symptoms
The
RCADS-P
contains the same six subscales as the RCADS and has previously
shown
good
psychometric
properties
with
school-based
(Ebesu-tani
et
al
2011)
and
clinical
samples
(Ebesutani
et
al
2010) For
the
current
sample
internal
consistency
values
for
RCADS-P
Total
Anxiety subscale were as follows a= 092 at Time 1 a= 091 at
Time 2 a= 094 at Time 3 a= 078 at Time 4 and a= 088 at Time 5
Internal
consistency
values
for
the
RCADS-P
MDD
subscale
were
as
follows
a=
078
at
Time
1
a=
088
at
Time
2
a=
091
at
Time
3
a= 060 at Time 4 and a= 092 at Time 5
24
Data
analytic
plan
For the present study we used piecewise LGCM to model
symptom trajectories over (1) the course of treatment and (2)
during the
six-month
follow-up
period
Several
indices
of
model
1047297t
were
used
including
chi square
comparative 1047297x index
(CFI)
root mean square error of approximation (RMSEA) and stan-
dardized root mean square residual (SRMR) For purposes of interpretation indices of good model 1047297t include a non-signi1047297cant
chi square ( p gt 005) CFI gt 095 RMSEA
lt 006 and SRMR lt 008
(Kline 2011) Signi1047297cant tests for parameter estimates were
conducted with the z -statistic using a two-tailed test LGCM
analyses were conducted using MPLUS Fifth version (Muthen amp
Muthen 2005)
3 Results
The data were
1047297rst screened for normality and to determine if
there were any statistical outliers Skewness and kurtosis levels
were within acceptable ranges (Kline 2011) No signi1047297cant
outliers ( z
3)
were
identi1047297ed
at
any
time
points
All
subjects
had complete data for Time 1 as well as at least one other post-baseline assessment Fifty-1047297ve subjects (9322) had data at the 8-
week assessment (Time 2) and 48 participants (8136) had data at
the
end
of
treatment
(M
=
1558
sessions)
assessment
(Time
3)
However
there
was
considerable
missing
data
at
the
two
follow-
up time points with 29 subjects (4915) having available data
three months after treatment (Time 4) and 24 participants
(4068)
having
data
six
months
after
treatment
(Time
5)
although
6271
of
subjects
had
available
data
for
at
least
one
follow-up time point Attrition analyses revealed no signi1047297cant
differences between those with complete data and those with
missing
data
on
any
indicators
of
symptom
severity
at
baseline
or
any
demographic
variables
(eg
age
gender
ethnicity)
Further-
more those with and without follow-up data did not show
signi1047297cant
differences
on
any
variables
at
the
post-treatmentassessment
31 Descriptive statistics
See
Table
3
for
observed
means
and
standard
deviations
of
RCADSRCADS-P
Total
Anxiety
T -scores
and
RCADSRCADS-P
MDD
T -scores at each time point In addition the percentage of
participants with T -scores 65 and T -scores 70 are presented
Mean
T -scores
on
all
four
measures
reduced
to
below
65
by
Time
3
indicating
that
mean
levels
of
both
self-rated
and
parent-rated
anxiety and depressive symptoms were within the normative
range by the end of treatment Analysis of percentages of
participants
with
T -scores
65
and
T -scores
70
also
revealed
reductions
in
those
with
borderline
elevated
and
clinically
elevated
Table 2
UP-A structure and content
Required
module
Suggested
number of
sessions
Techniquesskills Core UPUP-A principle(s) targeted
1 1ndash3 Psychoeducation of emotions functional assessment of
antecedents behaviors and consequences associated
with emotional experiences
Present-focused emotional awareness
2 1ndash3 Generalized emotion exposures practice of non-
judgmental awareness
Present-focused awareness preventing
emotional avoidance acceptance of emotion-
related physiological sensations3 1ndash3 Identifying thinking traps detective thinking skills
generating alternative thoughts problem-solving skills
Enhancing cognitive 1047298exibility
4 4+ Interoceptive exposures in-vivo exposures behavioral
activation
Preventing emotional avoidance acceptance of
physiological sensations facilitating exposure to
interoceptive and in-vivo emotional triggers
5 1ndash2 Skill consolidation relapse prevention
Optional module Suggested number of sessions Techniquesskills
1 As needed Motivational enhancement
2 0ndash3 Safety planning crisis management
3 0ndash3 (at least 1 recommended) Parenting skills
516 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 711
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 6: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/6.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 611
Francis 2000) at all
1047297ve time points The RCADS is a 47-item self-
report measure of anxiety and depressive symptoms that containssix distinct subscales based upon DSM-IV criteria separation
anxiety social phobia generalized anxiety disorder obsessive-
compulsive disorder panic disorder and major depressive disor-
der Respondents are asked to indicate how much each item
describes them using never (0) sometimes (1) often (2) or always
(3) A Total Anxiety subscale score is comprised of 37 items and
summed from responses to the
1047297ve anxiety subscales A major
depressive disorder (MDD) subscale score is comprised of 10 items
Raw
scores
were
converted
to
T -scores
using
child
age
and
gender
to place the two subscales on the same metric with
T-scores of 65
or greater indicating borderline levels of clinical severity and T-
scores of 70 and above representing clinically signi1047297cant elevations
(Weiss
amp
Chorpita
2011)
Internal
consistency
values
for
the
RCADS
Total Anxiety subscale were as follows a= 094 at Time 1 a= 095at Time 2 a= 091 at Time 3 a= 087 at Time 4 and a= 093 at Time
5 Internal consistency values for RCADS MDD subscale were as
follows
a=
085
at
Time
1 a=
090
at
Time
2
a=
091
at
Time
3
a=
091
at
Time
4
and a=
093
at
Time
5
233 Revised childrenrsquo s anxiety and depression scales ndash parent
version
The
adolescentrsquos parent
completed
the
Revised
Childrenrsquos
Anxiety and Depression Scales-Parent version (RCADS-P Ebesu-
tani Bernstein Nakamura Chorpita amp Weisz 2010) at all 1047297ve time
points
The
RCADS-P
is
a
47-item
parent-rated
measure
of
their
childadolescentrsquos
anxiety
and
depressive
symptoms
The
RCADS-P
contains the same six subscales as the RCADS and has previously
shown
good
psychometric
properties
with
school-based
(Ebesu-tani
et
al
2011)
and
clinical
samples
(Ebesutani
et
al
2010) For
the
current
sample
internal
consistency
values
for
RCADS-P
Total
Anxiety subscale were as follows a= 092 at Time 1 a= 091 at
Time 2 a= 094 at Time 3 a= 078 at Time 4 and a= 088 at Time 5
Internal
consistency
values
for
the
RCADS-P
MDD
subscale
were
as
follows
a=
078
at
Time
1
a=
088
at
Time
2
a=
091
at
Time
3
a= 060 at Time 4 and a= 092 at Time 5
24
Data
analytic
plan
For the present study we used piecewise LGCM to model
symptom trajectories over (1) the course of treatment and (2)
during the
six-month
follow-up
period
Several
indices
of
model
1047297t
were
used
including
chi square
comparative 1047297x index
(CFI)
root mean square error of approximation (RMSEA) and stan-
dardized root mean square residual (SRMR) For purposes of interpretation indices of good model 1047297t include a non-signi1047297cant
chi square ( p gt 005) CFI gt 095 RMSEA
lt 006 and SRMR lt 008
(Kline 2011) Signi1047297cant tests for parameter estimates were
conducted with the z -statistic using a two-tailed test LGCM
analyses were conducted using MPLUS Fifth version (Muthen amp
Muthen 2005)
3 Results
The data were
1047297rst screened for normality and to determine if
there were any statistical outliers Skewness and kurtosis levels
were within acceptable ranges (Kline 2011) No signi1047297cant
outliers ( z
3)
were
identi1047297ed
at
any
time
points
All
subjects
had complete data for Time 1 as well as at least one other post-baseline assessment Fifty-1047297ve subjects (9322) had data at the 8-
week assessment (Time 2) and 48 participants (8136) had data at
the
end
of
treatment
(M
=
1558
sessions)
assessment
(Time
3)
However
there
was
considerable
missing
data
at
the
two
follow-
up time points with 29 subjects (4915) having available data
three months after treatment (Time 4) and 24 participants
(4068)
having
data
six
months
after
treatment
(Time
5)
although
6271
of
subjects
had
available
data
for
at
least
one
follow-up time point Attrition analyses revealed no signi1047297cant
differences between those with complete data and those with
missing
data
on
any
indicators
of
symptom
severity
at
baseline
or
any
demographic
variables
(eg
age
gender
ethnicity)
Further-
more those with and without follow-up data did not show
signi1047297cant
differences
on
any
variables
at
the
post-treatmentassessment
31 Descriptive statistics
See
Table
3
for
observed
means
and
standard
deviations
of
RCADSRCADS-P
Total
Anxiety
T -scores
and
RCADSRCADS-P
MDD
T -scores at each time point In addition the percentage of
participants with T -scores 65 and T -scores 70 are presented
Mean
T -scores
on
all
four
measures
reduced
to
below
65
by
Time
3
indicating
that
mean
levels
of
both
self-rated
and
parent-rated
anxiety and depressive symptoms were within the normative
range by the end of treatment Analysis of percentages of
participants
with
T -scores
65
and
T -scores
70
also
revealed
reductions
in
those
with
borderline
elevated
and
clinically
elevated
Table 2
UP-A structure and content
Required
module
Suggested
number of
sessions
Techniquesskills Core UPUP-A principle(s) targeted
1 1ndash3 Psychoeducation of emotions functional assessment of
antecedents behaviors and consequences associated
with emotional experiences
Present-focused emotional awareness
2 1ndash3 Generalized emotion exposures practice of non-
judgmental awareness
Present-focused awareness preventing
emotional avoidance acceptance of emotion-
related physiological sensations3 1ndash3 Identifying thinking traps detective thinking skills
generating alternative thoughts problem-solving skills
Enhancing cognitive 1047298exibility
4 4+ Interoceptive exposures in-vivo exposures behavioral
activation
Preventing emotional avoidance acceptance of
physiological sensations facilitating exposure to
interoceptive and in-vivo emotional triggers
5 1ndash2 Skill consolidation relapse prevention
Optional module Suggested number of sessions Techniquesskills
1 As needed Motivational enhancement
2 0ndash3 Safety planning crisis management
3 0ndash3 (at least 1 recommended) Parenting skills
516 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 711
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 7: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/7.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 711
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 8: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/8.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 811
The 1047297nal model imposing equality constraints for the residual
variances of the
1047297rst three indicators and last two indicators
demonstrated acceptable model 1047297t by most indices
x2 (9) = 1363
p = 014 CFI = 097 RMSEA = 009 SRMR = 019
There was a signi1047297cant mean intercept (M i= 5368 SE = 165
p lt 0001) treatment slope factor (M s1= 476 SE = 074
p lt 0001)
and follow-up slope factor (M s2= 148 SE = 050 p lt 001) The
means of the slopes indicated that on average participantsrsquo RCADS
Total Anxiety T -scores decreased by 476 units every eight weeks
during treatment and by 148 units every eight weeks during the
follow-up period The variances for the intercept (di= 13072
SE = 2991 p lt 0001) treatment slope factor (ds1= 1532 SE = 623
p = 001) and follow-up slope factor (ds2= 515 SE = 217 p lt 002)
were all statistically signi1047297cant This indicated signi1047297cant variation
in participantsrsquo baseline anxiety symptom levels as well as
variability in the rate of change in anxiety symptom reduction
during treatment and follow-up The intercept and treatment slope
factor were signi1047297cantly correlated with one another
r = 059
p lt 0001 indicating that participants who reported greater
anxiety symptom severity at baseline demonstrated faster
symptom reduction during treatment In addition the treatment
and follow-up slopes were signi1047297cantly and negatively correlated
r = 051
p = 001 Participants who demonstrated faster anxiety
symptom reduction during treatment showed slower changeduring follow-up The intercept and follow-up slope factor were
not signi1047297cantly correlated
r = 023
p gt 030
322 Depressive symptoms
The 1047297nal model for self-rated depressive symptoms demon-
strated acceptable
1047297t by most indices
x2 (7) = 1042
p = 017
CFI = 098 RMSEA = 009 SRMR = 006 The residual variances of
the 1047297nal two indicators were constrained equal however
imposing equality constraints on the residual variances of the
1047297rst three time indicators did signi1047297cantly worsen model
1047297t
x2D
(2) = 1429 p lt 0001 and therefore these residual variances were
freely estimated
There was a signi1047297cant mean intercept (M i = 5791 SE = 181
p lt 0001) and treatment slope (M s1= 482 SE = 082
p lt 0001)
However contrary to the LGCM for adolescentsrsquo self-rated anxiety
symptoms the mean follow-up slope was not statistically
signi1047297cant (M s2= 067 SE = 055 p gt 020) The non-signi1047297cant
slope indicated that on average participants did not display
signi1047297cant reductions in self-rated depressive symptoms after
treatment ended The variances of the intercept (di = 18425
SE = 4274 p lt 0001) and treatment slope factor (ds1= 2716
SE = 1089
p = 001) were statistically signi1047297cant while the variance
of the follow-up slope factor approached statistical signi1047297cance
(ds2= 424 SE = 254 p = 009) Similar to the LGCM for self-rated
anxiety the intercept and treatment slope factor were signi1047297cantly
and positively correlated
r = 048
p
lt 001 while the intercept and
follow-up slope were non-signi1047297cantly correlated
r = 020
p = 042 However in contrast to the LGCM for self-rated anxiety
symptoms the treatment and follow-up slopes for self-rated
depressive symptom were not signi1047297cantly correlated
r = 024
p = 035
33 LGCMs for parent-rated symptoms
331 Anxiety
symptoms
Parent-rated anxiety and depressive symptom trajectories
(observed and estimated) are displayed in Fig 3 The piecewise
LGCM for RCADS-P Total Anxiety
T -scores demonstrated poor
1047297t
x2
(6) = 1427
p = 003 CFI = 091 RMSEA = 018 SRMR = 023 In
addition the follow-up slope factor mean was non-signi1047297cant
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Total Anxiety T -Scores
50
52
54
56
58
60
62
64
66
68
70
Baseline 8-Week Post 3-month fu 6-month fu
Observed
Estimated
RCADS-P Major Depressive Disorder T -Scores
Fig 3 Parent-rated symptom change during UP-A and follow-up
518 AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 9: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/9.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 911
(M s2= 116 p = 032) and had a non-signi1047297cant negative residual
variance forcing the residual variance to be
1047297xed at 0 Given poor
model 1047297t and little growth or variability during follow-up period
an LGCM with a single slope factor to represent change during both
treatment and follow-up was conducted
The
1047297rst three loadings were
1047297xed at 0 1 and 2 while the
last two time points were freely estimated Based upon modi1047297ca-
tion indices we 1047297xed the residual variances for the 1047297rst and last
time points to be equal and the residual variances for the second
third and fourth time points to be equal These equality constraints
did not signi1047297cantly worsen model
1047297t and this
1047297nal model showed
acceptable 1047297t x2 (11) = 1585 p = 015 CFI = 096 RMSEA = 010
SRMR = 023 The loadings for the last two time points of the single
slope factor were estimated at 297 and 326 respectively
indicating that reductions in RCADS-P Total Anxiety T -scores
quickly leveled out following the end of treatment
There was a statistically signi1047297cant intercept mean (M i= 6482
SE = 214
p
lt 0001) and slope mean (M s1= 409 SE = 070
p
lt 0001) The variance of the intercept was statistically signi1047297cant
(di = 18895 SE = 4383 p lt 0001) but the variance of the slope did
not reach statistical signi1047297cance (ds = 403 SE = 301 p = 018)
Similar to the LGCM for adolescent-rated anxiety there was a
signi1047297cant and positive correlation between intercept and slope
r = 081 p lt 0001
332
Depressive
symptoms
The piecewise model displayed poor
1047297tx2 (7) = 2114
p = 0004
CFI = 086 RMSEA = 021 SRMR = 021 and the follow-up slope
factor mean was non-signi1047297cant (M s2= 0004 p = 099) indicating
virtually no continued reduction in RCADS-P MDD
T -scores after
the end of treatment Therefore we speci1047297ed a single slope factor
and allowed the loadings for the 1047297nal two time points to be freely
estimated Modi1047297cation indices suggested allowing the residual
variance of the
1047297nal time point to be freely estimated while
constraining the residual variances of the 1047297rst four time points did
not signi1047297cantly worsen model 1047297t In addition it was recom-
mended
to
allow
the
residual
variances
of
the
fourth
and
1047297fth time
points to co-vary and the residual variances of the third and fourthtime points to co-vary The 1047297nal model demonstrated acceptable
1047297t x2 (9) = 1382 p = 013 CFI = 095 RMSEA = 011 SRMR = 014
The
loadings
for
the
1047297nal
two time
points
were
estimated
at 219
and 241
respectively
indicating
very
little
continued
reduction
in RCADS-P MDD T -scores during the follow-up period
The intercept mean was statistically signi1047297cant (M i = 6815
SE
=
244
p
lt
0001)
as
was
the
slope
mean
(M s1=
478
SE
=
102
p
lt
0001)
The
variance
of
the
intercept
was
statistically
signi1047297cant
(di = 20752 SE = 5527 p lt 0001) but the variance of the slope
failed to reach statistical signi1047297cance (di = 20752 SE = 5527
p
lt
0001)
The
intercept
and
slope
were
signi1047297cantly
and
positively
correlated
r
=
071 p
lt
001 Controlling
for
their
shared
association with the latent factor the residual variances for the
fourth
and
1047297fth time
points
were
signi1047297cantly
and
negativelycorrelated
r
= 075
p
lt
001 while
the
residual
variances
for
the
third
and
fourth
time
points
were
signi1047297cantly
positively
correlated r = 064 p lt 0001
4
Discussion
This study examined the separate trajectories of adolescent
anxiety and depressive symptom reduction over the course of a
transdiagnostic
emotion-focused
intervention
as
well
as
up
to
six
months
following
treatment
We
conducted
separate
piecewise
LGCMs for adolescent self-rated and parent-rated symptoms
Results from LGCMs for self-rated symptoms revealed similar rates
of
change
in
anxiety
(M
=
476)
and
depressive
symptoms
(M
=
482)
during
the
course
of
the
UP-A However
one
notable
difference was that whereas anxiety symptoms continued to show
signi1047297cant reduction during follow-up depressive symptoms
showed little change after treatment In addition the correlations
between change during treatment and change during follow-up
were stronger for anxiety symptoms compared to depressive
symptoms Results from LGCMs for parent-rated symptoms
showed poor model
1047297t for piecewise growth curves due to very
small symptom reduction in the six months following the end of
treatment This was true for both parent-rated anxiety and
depressive symptoms
These
1047297ndings may offer important implications First mean
rates of change for anxiety and depressive symptom reduction
were nearly equivalent during the treatment phase of the UP-A
These results suggest that the UP-A may effectively target anxiety
and depressive symptoms for adolescents with emotional dis-
orders These results are similar to prior work showing improve-
ments in both anxiety and depressive symptoms regardless of the
principal diagnosis in both anxiety-focused and depression-
focused CBT interventions (eg Kendall Safford Flannery-
Schroeder amp Webb 2004 Weisz et al 2006) However this
study differed in two important ways from prior work that may
offer particularly compelling evidence for this transdiagnostic
treatment First we actively recruited a more comorbid sample
than has been typically reported in prior CBT trials (eg Walkupet al 2008) with participants showing a high rate of anxiety and
depressive disorder comorbidity Second to our knowledge this
was the
1047297rst study to examine the separate rates of change in
anxiety and depression symptoms during treatment and follow-
up Thus our 1047297ndings add to prior work by suggesting that not only
do anxiety and depressive symptoms improve within a evidence-
based transdiagnostic intervention but that they also change at
similar rates during treatment
Although anxiety and depressive symptoms showed similar
rates of change during treatment our work also highlights they
may show important differences in reduction after treatment
Speci1047297cally within LGCMs for self-rated symptoms anxiety
symptoms
showed
continued
and
signi1047297cant
reduction
during
follow-up whereas depressive symptoms showed non-signi1047297cantreduction after treatment Although speculative in nature there
are potential explanations for these 1047297ndings Since this was a
primarily
anxious
sample
it
is
possible
that
relapse
prevention
efforts
were
focused
upon
techniques
geared
more
for
anxiety
(eg
exposure work) than depression (eg behavioral activation) As a
result adolescents may have perceived more opportunities to
practice
treatment
strategies
more
relevant
to
anxiety
than
depression
during
the
follow-up
phase
It
is
important
to
note
that other trials have also observed a plateau in depressive
symptom reduction for depression-focused CBT (The Treatment for
Adolescents
with
Depression
Study
(TADS)
2009) and
anxiety-
focused
CBT
(Kendall
et
al
1997)
Thus
our
1047297ndings
are
consistent
with prior work
Another
interesting
difference
was
that
while
treatment
andfollow-up
slopes
were
signi1047297cantly
and
negatively
correlated
for
self-rated
anxiety
symptoms
their
correlation
was
non-signi1047297cant
for depressive symptoms This 1047297nding suggests that the rate of
change during treatment is more strongly associated with change
during
follow-up
for
anxiety
symptoms
compared
to
depressive
symptoms
for
adolescents
receiving
the
UP-A However
this
result
may also be explained by less variance in the follow-up slope for
depressive symptoms compared to anxiety symptoms The
negative
correlation
observed
for
anxiety
symptoms
may
be
explained
by
less
room
for
improvement
for
participants
who
had
greater symptom change during treatment
Finally there were observed differences between adolescent
self-rated
and
parent-rated
symptom
change
Parent-rated
symp-
tom
models
showed
poor
1047297t to
piecewise
growth
curves
as
a
result
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 519
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 10: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/10.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1011
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
response
and
childhood
anxiety
Association
with
symptoms
of anxiety disorders and cognitive bias Journal of Clinical Child and Adolescent Psychology 34(4) 712ndash723 httpdxdoiorg101207s15374424jccp3404_13
Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521
![Page 11: Queen, 2014](https://reader036.fdocuments.us/reader036/viewer/2022062400/5695d1941a28ab9b029719b4/html5/thumbnails/11.jpg)
7212019 Queen 2014
httpslidepdfcomreaderfullqueen-2014 1111
Fox N A Nichols K E Henderson H A Rubin K Schmidt L Hamer D amp Pine DS (2005) Evidence for a gene-environment interaction in predicting behavioralinhibition in middle childhood Psychological Science 16(12) 921ndash926 httpdxdoiorg101111j1467-9280200501637x
Garber J amp Weersing V (2010) Comorbidity of anxiety and depression in youthImplications for treatment and prevention Clinical Psychology science and practice 17 (4) 293ndash306 httpdxdoiorg101111j1468-2850201001221x
Ginsburg G S Kendall P C Sakolsky D Compton S N Piacentini J Albano A ampMarch J (2011) Remission after acute treatment in children and adolescentswith anxiety disorders Findings from the CAMS Journal of Consulting andClinical Psychology 79(6) 806ndash813 httpdxdoiorg101037a0025933
Kagan
J
Reznick
J
amp
Snidman
N
(1987)
Temperamental
variation
in
response
tothe unfamiliar In NA Krasnegor EM Blass amp MA Hofer (Eds) Perinataldevelopment a psychobiological perspective (pp 421ndash440) San Diego CAAcademic Press
Kendall P C Flannery-Schroeder E Panichelli-Mindel S M Southam-Gerow MHenin A amp Warman M (1997) Therapy for youths with anxiety disorders Asecond randomized clinical trial Journal of Consulting and Clinical Psychology 65(3) 366ndash380 httpdxdoiorg1010370022-006X653366
Kendall P C Safford S Flannery-Schroeder E amp Webb A (2004) Child anxietytreatment Outcomes in adolescence and impact on substance use anddepression at 74-year follow-up Journal of Consulting and Clinical Psychology72(2) 276ndash287 httpdxdoiorg1010370022-006X722276
Kline R B (2011) Principles and practice of structural equation modeling 3rd ed NewYork NY Guilford Press
McHugh R amp Barlow D H (2010) The dissemination and implementation of evidence-based psychological treatments A review of current efforts AmericanPsychologist 65(2) 73ndash84 httpdxdoiorg101037a0018121
Miller W R amp Rollnick S (2002) Motivational interviewing Preparing people for change 2nd ed New York US Guilford Press
OrsquoNeil
K
A
amp
Kendall
P
C
(2012)
Role
of
comorbid
depression
and
co-occurringdepressive symptoms in outcomes for anxiety-disordered youth treated withcognitive-behavioral therapy Child amp Family Behavior Therapy 34(3) 197ndash209httpdxdoiorg101080073171072012707086
Ollendick T H Shortt A L amp Sander J B (2005) Internalizing disorders of childhood and adolescence In JE Maddux BA Winstead JE Maddux amp BAWinstead (Eds) Psychopathology foundations for a contemporary understanding (pp 353ndash376) Mahwah NJ Lawrence Erlbaum Associates Publishers
Silverman W K amp Albano A M (1996) Anxiety disorders interview schedule forDSM-IV Child and parent versions San Antonio psychological corporation
Stark K D amp Laurent J (2001) Joint factor analysis of the Childrens Depression IInventoryandtheRevisedChildrensManifestAnxietyScale Journalof ClinicalChildPsychology 30(4) 552ndash567 httpdxdoiorg101207S15374424JCCP3004_11
Stavrakaki C Vargo B Boodoosingh L amp Roberts N (1987) The relationshipbetween anxiety and depression in children Rating scales and clinical variablesThe Canadian Journal of PsychiatryLa Revue Canadienne de Psychiatrie 32(6)433ndash439
The Treatment for Adolescents with Depression Study (TADS) (2009) Outcomesover 1 year of naturalistic follow-up The American Journal of Psychiatry 166(10)
1141ndash
1149
httpdxdoiorg101176appiajp200908111620Treatment for Adolescents with Depression Study (TADS) Team (2004) Fluoxetinecognitive-behavioral therapy and their combination for adolescents withdepression Treatment for Adolescents With Depression Study (TADS)randomized controlled trial Journal of the American Medical Association 292(7) 807ndash820 httpdxdoiorg101001jama2927807
Trosper S E Buzzella B A Bennett S M amp Ehrenreich J T (2009) Emotionregulation in youth with emotional disorders Implications for a uni1047297edtreatment approach Clinical Child and Family Psychology Review 12(3) 234ndash254httpdxdoiorg101007s10567-009-0043-6
Trosper S E Whitton S W Brown T A amp Pincus D B (2012) Understanding thelatent structure of the emotional disorders in children and adolescents Journalof Abnormal Child Psychology 40(4) 621ndash632 httpdxdoiorg101007s10802-011-9582-7
Walkup J T Albano A Piacentini J Birmaher B Compton S N Sherrill J T ampKendall P C (2008) Cognitive behavioral therapy sertraline or a combinationin childhood anxiety The New England Journal of Medicine 359(26) 2753ndash2766httpdxdoiorg101056NEJMoa0804633
Weems C F Zakem A H Costa N M Cannon M F amp Watts S E (2005)
Physiological
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anxiety
Association
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symptoms
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Weiss D C amp Chorpita B F (2011) Revised childrenrsquos anxiety and depression scaleuserrsquos guide Los Angeles University of California Unpublished manuscript
Weisz J R McCarty C A amp Valeri S M (2006) Effects of psychotherapy fordepression in children and adolescents A meta-analysis Psychological Bulletin132(1) 132ndash149 httpdxdoiorg1010370033-29091321132
AH Queen et al Journal of Anxiety Disorders 28 (2014) 511ndash521 521