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acta psychiatr scand 2008 1 9 copyright 2008 the authors all rights reserved actapsychiatrica doi 10 1111 j 1600 0447 2008 01270 x scandinavica review group cognitive behavioural therapy for ...

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            Acta Psychiatr Scand 2008: 1–9                                                        Copyright  2008 The Authors
            All rights reserved                                                                     ACTAPSYCHIATRICA
            DOI: 10.1111/j.1600-0447.2008.01270.x                                                     SCANDINAVICA
            Review
            Group cognitive behavioural therapy for
            obsessive–compulsive disorder: a systematic
            review and meta-analysis
               ´                                                                                       1,2              1
              Jonsson H, Hougaard E. Group cognitive behavioural therapy for               H. Jnsson , E. Hougaard
              obsessive–compulsive disorder: a systematic review and meta-analysis.        1
                                                                                           Department of Psychology, University of Aarhus,
                                                                                                   2
                                                                                           Aarhus and Clinic for Obsessive Compulsive Disorder,
              Objective: Behaviour therapy with exposure and response prevention           Aarhus University Hospital, Risskov, Denmark
              (ERP) or cognitive behavioural therapy (CBT) including ERP are
              considered the psychological treatments of choice for obsessive–
              compulsive disorder (OCD), but group CBT⁄ERP has received
              relatively little research attention in the treatment of OCD. The aim of
              this study was to provide a meta-analysis of the effectiveness of group
              CBT⁄ERPfor OCD.
              Method: A systematic literature search was conducted and studies
              were meta-analysed by means of the Cochrane Review Manager
              Program with measures of i) pre- to post-effect sizes (ES) and
              ii) between-group ES in comparison with different control conditions.
              Outcome was primarily measured on the Y-BOCS and ES was
              calculated in the form of Cohens d.
              Results: Thirteen trials were included in the meta-analysis. The overall
              pre–post-ES of these trials of 1.18 and a between-group ES of 1.12
              compared with waiting list control in three randomized controlled
              studies indicate that group CBT⁄ERP is an effective treatment for             Key words: obsessive–compulsive disorder; meta-
              OCD. Group CBT achieved better results than pharmacological                  analysis; cognitive behavioural therapy; group therapy
              treatment in two studies. One study found no significant differences           Hjalti Jnsson, Department of Psychology, University of
              between individual and group CBT.                                            Aarhus, Jens Chr. Skous Vej 4, 8000 Aarhus, Denmark.
              Conclusion: Group CBT is an effective treatment for OCD, but more             E-mail: hjalti@psy.au.dk
              studies are needed to compare the effectiveness of group and individual
              treatment formats.                                                           Accepted for publication August 21, 2008
             Summations
              •   Group cognitive behavioural therapy including exposure and response prevention is an effective
                  treatment for obsessive–compulsive disorder.
              •   There are insufficient data on the relative effectiveness of individual and group cognitive behavioural
                  therapy including exposure and response prevention for obsessive–compulsive disorder.
             Considerations
              •   There are few studies of the effectiveness of group cognitive behavioural therapy including exposure
                  and response prevention for obsessive–compulsive disorder and only four randomized control trials.
            Introduction                                                 debilitatingdisorderwithachroniccourseifuntreated.
                                                                         Epidemiological studies have found lifetime preva-
            Obsessive–compulsive disorder (OCD) is character-            lence estimates of OCD to be about 1–2% (2, 3).
            ized by persistent, intrusive thoughts (obsessions)            Overthelasttwodecades,researchershavemade
            and⁄or stereotyped repetitive behaviours carried out         progress in identifying effective treatments includ-
            in a ritualistic fashion (compulsions) (1). It is a          ing psychotherapy, pharmacotherapy and their
                                                                                                                               1
                  ´
                Jonsson and Hougaard
                combination.ThepsychologicaltreatmentforOCD              of Science and The National Research Register,
                with the highest degree of empirical support is          from the first available year to 01.02.07, using the
                individualexposureandresponseprevention(ERP)             keywords [(obsess* or compul* or ocd) AND
                (4, 5). Most clinicians today, however, supplement       (group next therap*) OR (group next treatment*)].
                the behavioural methods with cognitive methods,          In addition, the reference lists of other reviews and
                although there is at present no empirical evidence       selected articles were inspected for further relevant
                showing that cognitive behavioural therapy (CBT)         studies.
                withERPachievesbetteroutcomesthanERPalone
                (4). Meta-analyses suggest that ERP and CBT with         Inclusion criteria
                ERPachievelarge effects in pre–post-conditions or
                compared with waitlist or placebo conditions. For        The following criteria were used for inclusion of
                example,Eddyet al.(6)foundanuncontrolled,pre–            studies: i) participants aged 18 years or above, ii) a
                post-effect size (ES) of 1.52 (Cohens d) in a meta-      primary diagnosis of OCD according to a stan-
                analysis of 13 randomized controlled trials (RCTs)       dardized diagnostic classification system (e.g.
                andacontrolled,between-groupESof1.12basedon              DSM-III or later editions), iii) interventions in
                three of these studies. In the same review, a meta-      the form of group ERP or group CBT, iv)
                analysis of 32 RCTs of pharmacological treatment         outcomes reported with means and standard devi-
                for OCD reported an uncontrolled pre–post-ES of          ations on the Yale-Brown Obsessive–Compulsive
                1.18 and a controlled, between-group ES of 0.83.         Scale (Y-BOCS) [clinical rating form or self-report
                Acomparisonofpre–post-ESforERPtreatmentof                version (only one study (9) used self-report ver-
                110patientsinanaturalistictreatmentsettingfound          sion)], v) number of participants in each treatment
                outcomessimilartothoseachievedinfourRCTs(7)              condition ‡10, vi) studies available in English or
                thusindicatingthatthemethodiseffectiveoruseful            German language and vii) published in peer-
                in general clinical practice.                            reviewed journals.
                  Group CBT⁄ERP for OCD has been proposed                  Exclusion criteria: i) studies limited to patients
                as a cost-effective treatment format. In a qualita-       with only hoarding symptoms or patients with
                tive review of 12 studies of group CBT or ERP for        obsessions only, ii) studies where patients received
                adults Himle, Van Etten and Fischer (8) concluded        combined individual and group therapy, and iii)
                that there was some evidence of the effectiveness of      studies where the duration of treatment was more
                group CBT or ERP, although limitations in                than 20 weeks.
                quantity and quality of the research made conclu-          All decisions on inclusion⁄exclusion criteria were
                sions rather tentative. The meta-analysis by Eddy        made a priori. Two authors were contacted
                et al. (6) found somewhat larger uncontrolled, pre–      because of missing statistical information; Fals-
                post-ESs for individual therapy (1.48) than for          Stewart (10), and Sousa (11), and the needed
                group therapy (1.17). However, only two studies          information from the second-mentioned author
                on group treatment were included in their analysis       was retrieved.
                and the authors did not report whether the
                difference reached statistical significance.               Methodological quality of studies
                Aims of the study                                        Studies were ranked into three categories:
                Theaimofthisstudywastoprovideameta-analysis               i)  Randomized controlled studies; i.e. studies
                of group cognitive behavioural therapy (CBT) and              comparing group ERP or group CBT to
                exposure and response prevention (ERP) for OCD,               placebo control, waitlist control or to other
                whichhasnot,asfarasweknow,beendonebefore.                     active treatments.
                Thereview primarily analyses the overall pre–post-        ii) Controlled studies; i.e. studies with control
                effect size (ES) of group CBT and ERP therapy for              conditions but without randomized group
                OCD and, secondarily, between-group ESs for                   allocation.
                different control conditions.                             iii) Open clinical trials with outcome measures
                                                                              before and after therapy but no control
                                                                              conditions.
                Material and methods                                       Quality of individual studies was independently
                Identification of studies                                assessed, by the two authors of the paper, on the
                                                                         Cochrane Collaboration Depression, Anxiety and
                Studies were located by searching the following          Neurosis Group (CCDAN) quality rating scale a
                databases: PsychInfo, EBSCO host, PubMed, Web            23-item scale with total scores from 0 to 46 (12).
                2
                                                                                                       Group CBT for OCD
            The consistency between the two raters was                  Results
            acceptable with a Cronbachs a value of 0.93. In            Trial flow
            case of a substantial disagreement (>3 points on
            the scale), the differences were discussed and new           The electronic search strategy yielded 1749 publi-
            consensual ratings were applied.                            cations. After abstract screening, 37 studies were
                                                                        retrieved for more detailed evaluation with two
            Statistical analysis                                        additional studies found from references. Based on
                                                                        inspection of papers, 13 primary studies were
            DatafromtheY-BOCSwereconsideredasprimary                    judged to fulfil the inclusion criteria; four RCTs
            outcome measures. Data were entered into the                (11, 18–20), four controlled studies (21–24) and five
            computer software review manager 4.2 (RevMan),              open studies (9, 25–28). A list of excluded studies
            provided by The Cochrane Collaboration (13). For            and reasons for exclusion are available on request
            continuous outcomes, the software calculates stan-          from the corresponding author.
            dardized weighted mean difference based on
            Cohens (14) d and 95% confidence intervals. The             Study characteristics
            random-effects model was used, which yields supe-
            rior results in terms of clinical interpretability and      Table 1 summarizes selected characteristics of the
            external generalizibility to other clinical contexts        13 studies. Number of participants in the studies
            compared with analyses based on the fixed effects             varied from 20 to 155 with a total of 828
            model (15). The RevMan software calculates two              participants. Of these, a total of 549 received
            additional statistics for estimating heterogeneity of       group therapy (395 group CBT and 154 group
                                      2                          2      ERP), 79 functioned as waitlist controls, 83
            studies, the I-squared (I ) and Q-statistics. The I
            statistics indicates the percentage of variance in a        received pharmacological treatment, 25 received
            pooledESthatcanbeattributedtoheterogeneityin                individual CBT, 17 received group relaxation
            the sample of studies (16). Values of 25% are               training and 75 received other sorts of active
            consideredlow,50%asmoderateand75%ashigh.                    treatments (50 received a mixture of group therapy
            TheQ-statistics calculates P-values for heterogene-         and pharmacotherapy and 20 received multifamily
            ity of studies (i.e. P-values £0.05 indicates signif-       group ERP).
            icant heterogeneity).                                         Mean age of the group treatment sample was
              As a supplement to these analyses, Fail-Safe N            36.4 years, about 63% was females, and approxi-
            was calculated as a measure of how vulnerable               mately 54% was in pharmacological treatment at
            meta-analysis ES findings are to the possibility of          treatment onset. The overall mean on the Y-BOCS
            undiscoveredstudies (17). Fail-Safe N estimates the         scale at inclusion was 23.4 (SD = 1.62, range
            number of undiscovered, approximately equally               21.2–26.7). There were no significant differences in
            sized studies with an ES of zero needed to reduce           Y-BOCS scores at treatment start between the
            the overall ES to a certain criterion level, e.g. to 0.5    three  categories   of studies [F(2, 12) = 0.519
            or 0.2, ESs classified as medium and small by                P=0.608]. Treatment duration ranged from
            Cohen (14).                                                 seven to 16 weekly sessions with an average of 11
              ByusingtheRevMansoftware,pooledmeanpre–                   sessions with each session lasting 1½–2½ h (mean
            post-ES, weighted according to numbers of partic-           120 min). Group sizes varied from four to 10
            ipants in the studies, were computed for each of the        participants (mean 6.8) with one or two therapist(s)
            three methodological categories as well as for total        in each group. Follow-up ratings were obtained in
            number of studies. Between-group ES were calcu-             nine of the included studies, and the follow-up
            lated for comparisons of group CBT⁄ ERP to i)               period ranged from 1 month to 4 years, with an
            waitlist control group, ii) placebo control, iii)           average    of   12.3 months     (median    3 months)
            individual CBTandiv)pharmacologicaltreatment.               (follow-up data are not analysed in this study).
              In case of evidence of marked heterogeneity               Drop-out rate was 13.5% in group treatment,
              2                                                         compared with 8.5% in other treatments and
            (I > 50%) studies with markedly higher⁄lower
            ES were tentatively considered as outliers and              11.4% in the waiting list control conditions.
            excluded from the analysis. A sensitivity analysis
            was then conducted comparing meta-analyses with             Quantitative data synthesis
            and without the outliers checking for significant
            differences.                                                Thirteen studies were included in the meta-anal-
              In addition, overall pooled mean pre–post-ESs             ysis with 15 comparisons. Separate analyses were
            were computed for other outcome measures of                 performed on CBT and ERP group therapy in
            symptoms of depression and anxiety.                         McLean et al. (20) and on participants receiving
                                                                                                                             3
           ´
          Jonsson and Hougaard
                CCDAN*2929     32.5  28    26  19.5 18.5 20     20 24
              -BOCS7.37.30.610.87.411.61.55.09.70.86.45.48.38.92.97.26.77.38.65.712.6
             Meanchange         ii)            i)ii)iii)ii)     )
              Y    i)ii)iii)i)ii)i)  i)ii)iii)i)ii) i)   i)ii)  i  i)
             sizeof(2)  (1)    (2)   (2)   (1)(1)
                   5–7  5–8    7–8   6–8   7–94–75–85–8  7–85   R
             Grouptherapists))                 )
              (numberi) i      i)    i)    i)ii)iii)NR   i)ii)  N  5–8
                                                    +  49.9
                                                     term
                Follow-upmonth monthsmonthsmonths   monthslong(meanmonths)monthsmonths
                   1    –      3     3     12  –    3    12     –  3
                                                     h
                                                    72           ses-
              reatmentdurationweeklysessionsweeklysessionsweeklysessionsweeklysessionsweeklysessionsweeklysessionsorweeklysessionsweeklyhweeklysession
              T     h    h      h     h      h  h           h        h
                   102  122    122   122   122 102  12weeklysessions10–122102.5sions122
                         prior months      to
                   months      3     months  during        not
                   3                 3                      how
                    treatmentmonthtreatmenttreatmentalloweddosesstablefor
                medicationstable1stablestablenot
                On  to          to    to             kept  stable-but
                   63%  0%stabletreatment44,7%48%34%0%60%       36%56.2%
                   i)priori)ii)toi)priori)priori)increasetreatmenti)i)NotNRKeptreportedlongi)i)
              (SD) (NR) (11.57)(11.2)      (NR)(10.3)              (11.2)
             Meandisorder13.623.521.8      18.517.4                23.6
              durationofi)i)   i)    NR    i)  i)   NR   NR     NR i)
              of(SD)(NR)(7.58) (6.64)          (7.2)            (9.02)(6.64)
             Meanageonset19.91514.7            19.6             10.715
                   i)   i)     i)    NR    NR  i)   NR   NR     i) i)
                   67.9 80     51    48    83  NR   62   67     78 69
              Percentwomeni)i) i)    i)    i)       i)   i)        i)
                (SD)(NR)(11.79)(12.8)(NR)  (NR)(NR) (10.86)(NR) (8.85)(12.8)
              Meanage33.738.5  36.5  35    39.534.1 37   33.0   34.839.5
                                                                )  )
                   i)   i)     i)    i)    i)  i)   i)   i)     i  i
                    5 3  3      1     35     6  2 0  NR    1
                   4⁄ ⁄ 3⁄     1⁄    1⁄⁄   1 ⁄ 10⁄⁄ NR⁄  5 ⁄    8  2
              drop-⁄  17⁄      ⁄     ⁄ 38  ⁄   ⁄  55⁄    ⁄      ⁄  ⁄
              ⁄ outs21252828   2324  1919  24174555 2489 2220   53 32
              n    i)ii)iii)i)ii)i)ii)i)ii)iii)i)ii)i)ii)iii)i)ii)i)ii)i)i)
                        or     brain
                         16),severe                             abuse
                         >     risk; mentalsevereother
                                phobia,,     24 ,                  suicidalsevere(borderline
                    mentalmoderate(BDIabuse,severeseverementaland>alcohol,
                criteria   psychotic   physical   diagnosis,       withmental
                   intellectual,suicidalsocialdisorderdisorders,epilepsyI
                             disorderwithdisordersorganicMADRS       disorderdisorder
                    organic substancenervosa,severepsychosisaxis
                Exclusion,syndrome,depressiondisorder,retardation,,s,symptoms;
                        ´s      severethought physical            depression
                                ,                                    bipolar
                                          studies                      schizotypical),
                    disabilitydisorderouretteseverebipolardisorderpersonalityDepressioninjurymentalanorexiapersonalityActiveretardation,disorderdisordersourettedepressionschizophrenia,comorbidNRNRrisk,personalityorretardation
                   Schizophrenia,T         T   Severe           PsychoticMajor
           studies                              +   –  –
                                       –  controlled
           include CBT  CBT    CBT   CBTERPCBTRTCBTCBTERPERPERPERPCBTCBT
           of          aitlist  aitlistaitlist       weeksweeks
                InterventionGroupIndividualCBTWGroupSertralineGroupWGroupGroupWdelayedGroupGroup-basedGroupGroupmedicationMedicationGroup12Group7GroupMultifamilygroupGroupGroup
                   i)ii)iii)i)ii)i)ii)i)ii)iii)i)ii)i)ii)iii)i)ii)i)ii)studiesi)i)
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           1.            al.    al.   al.    al.al.  al. Noppenal.al.al.
                    Rees et     et    et     et et   et  n et    et  et
                                                         a
           able    AndersonSousaCordioliMcLeanFinebergAignerHimleVMeierCordioli
           T    StudyCategory             Category            Category
          4
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...Acta psychiatr scand copyright the authors all rights reserved actapsychiatrica doi j x scandinavica review group cognitive behavioural therapy for obsessive compulsive disorder a systematic and meta analysis jonsson h hougaard e nsson department of psychology university aarhus clinic objective behaviour with exposure response prevention hospital risskov denmark erp or cbt including are considered psychological treatments choice ocd but has received relatively little research attention in treatment aim this study was to provide eectiveness erpfor method literature search conducted studies were analysed by means cochrane manager program measures i pre post eect sizes es ii between comparison dierent control conditions outcome primarily measured on y bocs calculated form cohens d results thirteen trials included overall these compared waiting list three randomized controlled indicate that is an eective key words achieved better than pharmacological two one found no signicant dierences hj...

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