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HEALTH TECHNOLOGY ASSESSMENT VOLUME 19 ISSUE 101 DECEMBER 2015 ISSN 1366-5278 A randomised controlled trial of computerised cognitive behaviour therapy for the treatment of depression in primary care: the Randomised Evaluation of the Effectiveness and Acceptability of Computerised Therapy (REEACT) trial Elizabeth Littlewood, Ana Duarte, Catherine Hewitt, Sarah Knowles, Stephen Palmer, Simon Walker, Phil Andersen, Ricardo Araya, Michael Barkham, Peter Bower, Sally Brabyn, Gwen Brierley, Cindy Cooper, Linda Gask, David Kessler, Helen Lester, Karina Lovell, Usman Muhammad, Glenys Parry, David A Richards, Rachel Richardson, Debbie Tallon, Puvan Tharmanathan, David White and Simon Gilbody on behalf of the REEACT Team DOI 10.3310/hta191010 A randomised controlled trial of computerised cognitive behaviour therapy for the treatment of depression in primary care: the Randomised Evaluation of the Effectiveness and Acceptability of Computerised Therapy (REEACT) trial Elizabeth Littlewood,1 Ana Duarte,2 Catherine Hewitt,3 Sarah Knowles,4,5 Stephen Palmer,2 Simon Walker,2 Phil Andersen,1 Ricardo Araya,6,7 Michael Barkham,8 Peter Bower,5 Sally Brabyn,1 Gwen Brierley,1,9 Cindy Cooper,10 Linda Gask,5 David Kessler,11 Helen Lester,5,12† Karina Lovell,13 Usman Muhammad,3 Glenys Parry,10 David A Richards,1,14 Rachel Richardson,1 Debbie Tallon,15 Puvan Tharmanathan,3 David White10 and Simon Gilbody1* on behalf of the REEACT Team 1Department of HealthSciences, University of York, York, UK 2Centre forHealth Economics, University ofYork, York, UK 3YorkTrials Unit,Department ofHealth Sciences, University ofYork, York, UK 4Centre forPrimary Care, Institute ofPopulation Health, University ofManchester, Manchester, UK 5National Institute for HealthResearch (NIHR) School for PrimaryCare Research, Manchester Academic Health Science Centre,University ofManchester, Manchester, UK (previously National Primary CareResearch and Development Centre,University ofManchester, Manchester, UK) 6Academic Unit of Psychiatry, University ofBristol, Bristol, UK 7DepartmentofPopulationHealth,LondonSchoolofHygieneandTropicalMedicine,London,UK 8Centre forPsychological Services Research, University ofSheffield, Sheffield, UK 9Medical Research Council (MRC) Epidemiology Unit, University of Cambridge School ofClinical Medicine, Cambridge, UK 10Clinical Trials Research Unit, School ofHealth and Related Research, University of Sheffield, Sheffield, UK 11Academic Unit ofPrimary Health Care, University of Bristol, Bristol, UK 12Primary CareClinical Sciences, University ofBirmingham, Birmingham, UK 13School ofNursing, Midwifery and Social Work, University of Manchester, Manchester, UK 14University ofExeter Medical School, University ofExeter, Exeter, UK 15School ofSocial & Community Medicine, University ofBristol, Bristol, UK *Corresponding author †In memoriam Declared competing interests of authors: SimonGilbody isaHealth Technology Assessment Clinical Evaluation and Trials Board Member.Michael Barkham isa developer of the Clinical Outcomes in Routine Evaluation –Outcome Measure, which was used as asecondary outcome measure in thetrial. Peter Bower reports personal fees from paid consultancy for theBritish Association of Counselling and Psychotherapy, outside thesubmitted work. Karina Lovell is aNon-Executive Director for Manchester Mental Health and Social Care Trust and is paidasalary. Published December 2015 DOI: 10.3310/hta191010 This reportshould be referenced as follows: Littlewood E, Duarte A, Hewitt C, Knowles S, Palmer S, Walker S, et al. Arandomised controlled trial of computerised cognitive behaviour therapy for the treatment of depression in primary care: theRandomised Evaluation of the Effectiveness andAcceptability of Computerised Therapy (REEACT) trial. Health Technol Assess 2015;19(101). HealthTechnology Assessment isindexed and abstracted in IndexMedicus/MEDLINE, Excerpta Medica/EMBASE, ScienceCitation Index Expanded (SciSearch®) andCurrent Contents®/ Clinical Medicine. Health Technology Assessment HTA/HTATAR ISSN1366-5278(Print) ISSN2046-4924(Online) Impactfactor:5.116 HealthTechnologyAssessmentisindexedinMEDLINE,CINAHL,EMBASE,TheCochraneLibraryandtheISIScienceCitationIndexandis assessedforinclusionintheDatabaseofAbstractsofReviewsofEffects. ThisjournalisamemberofandsubscribestotheprinciplesoftheCommitteeonPublicationEthics(COPE)(www.publicationethics.org/). Editorialcontact:[email protected] ThefullHTAarchiveisfreelyavailabletoviewonlineatwww.journalslibrary.nihr.ac.uk/hta.Print-on-demandcopiescanbepurchasedfromthe reportpagesoftheNIHRJournalsLibrarywebsite:www.journalslibrary.nihr.ac.uk CriteriaforinclusionintheHealthTechnologyAssessmentjournal ReportsarepublishedinHealthTechnologyAssessment(HTA)if(1)theyhaveresultedfromworkfortheHTAprogramme,and(2)they areofasufficientlyhighscientificqualityasassessedbythereviewersandeditors. ReviewsinHealthTechnologyAssessmentaretermed'systematic'whentheaccountofthesearchappraisalandsynthesismethods(to minimisebiasesandrandomerrors)would,intheory,permitthereplicationofthereviewbyothers. HTAprogramme TheHTAprogramme,partoftheNationalInstituteforHealthResearch(NIHR),wassetupin1993.Itproduceshigh-qualityresearch informationontheeffectiveness,costsandbroaderimpactofhealthtechnologiesforthosewhouse,manageandprovidecareintheNHS. ‘Healthtechnologies’arebroadlydefinedasallinterventionsusedtopromotehealth,preventandtreatdisease,andimproverehabilitation andlong-termcare. ThejournalisindexedinNHSEvidenceviaitsabstractsincludedinMEDLINEanditsTechnologyAssessmentReportsinformNationalInstitute forHealthandCareExcellence(NICE)guidance.HTAresearchisalsoanimportantsourceofevidenceforNationalScreeningCommittee(NSC) policydecisions. FormoreinformationabouttheHTAprogrammepleasevisitthewebsite:http://www.nets.nihr.ac.uk/programmes/hta Thisreport TheresearchreportedinthisissueofthejournalwasfundedbytheHTAprogrammeasprojectnumber06/43/05.Thecontractualstartdate wasinMay2009.ThedraftreportbeganeditorialreviewinJanuary2014andwasacceptedforpublicationinSeptember2014.Theauthors havebeenwhollyresponsibleforalldatacollection,analysisandinterpretation,andforwritinguptheirwork.TheHTAeditorsandpublisher havetriedtoensuretheaccuracyoftheauthors’reportandwouldliketothankthereviewersfortheirconstructivecommentsonthedraft document.However,theydonotacceptliabilityfordamagesorlossesarisingfrommaterialpublishedinthisreport. ThisreportpresentsindependentresearchfundedbytheNationalInstituteforHealthResearch(NIHR).Theviewsandopinionsexpressedby authorsinthispublicationarethoseoftheauthorsanddonotnecessarilyreflectthoseoftheNHS,theNIHR,NETSCC,theHTAprogramme ortheDepartmentofHealth.Ifthereareverbatimquotationsincludedinthispublicationtheviewsandopinionsexpressedbythe intervieweesarethoseoftheintervieweesanddonotnecessarilyreflectthoseoftheauthors,thoseoftheNHS,theNIHR,NETSCC,theHTA programmeortheDepartmentofHealth. ©Queen’sPrinterandControllerofHMSO2015.ThisworkwasproducedbyLittlewoodetal.underthetermsofa commissioningcontractissuedbytheSecretaryofStateforHealth.Thisissuemaybefreelyreproducedforthepurposesof privateresearchandstudyandextracts(orindeed,thefullreport)maybeincludedinprofessionaljournalsprovidedthat suitableacknowledgementismadeandthereproductionisnotassociatedwithanyformofadvertising.Applicationsfor commercialreproductionshouldbeaddressedto:NIHRJournalsLibrary,NationalInstituteforHealthResearch,Evaluation,Trials andStudiesCoordinatingCentre,AlphaHouse,UniversityofSouthamptonSciencePark,SouthamptonSO167NS,UK. PublishedbytheNIHRJournalsLibrary(www.journalslibrary.nihr.ac.uk),producedbyPrepressProjectsLtd,Perth,Scotland (www.prepress-projects.co.uk). Editor-in-Chief of Health Technology Assessment and NIHR Journals Library Professor Tom Walley Director, NIHR Evaluation, Trials and Studies and Director of the HTA Programme, UK NIHR Journals Library Editors Professor Ken Stein Chair of HTA Editorial Board and Professor of Public Health, University of Exeter Medical School, UK Professor Andree Le May Chair of NIHR Journals Library Editorial Group (EME, HS&DR, PGfAR, PHR journals) Dr Martin Ashton-Key Consultant in Public Health Medicine/Consultant Advisor, NETSCC, UK Professor Matthias Beck Chair in Public Sector Management and Subject Leader (Management Group), Queen’s University Management School, Queen’s University Belfast, UK Professor Aileen Clarke Professor of Public Health and Health Services Research, Warwick Medical School, University of Warwick, UK Dr Tessa Crilly Director, Crystal Blue Consulting Ltd, UK Dr Peter Davidson Director of NETSCC, HTA, UK Ms Tara Lamont Scientific Advisor, NETSCC, UK Professor Elaine McColl Director, Newcastle Clinical Trials Unit, Institute of Health and Society, Newcastle University, UK Professor William McGuire Professor of Child Health, Hull York Medical School, University of York, UK Professor Geoffrey Meads Professor of Health Sciences Research, Health and Wellbeing Research and Development Group, University of Winchester, UK Professor John Norrie Health Services Research Unit, University of Aberdeen, UK Professor John Powell Consultant Clinical Adviser, National Institute for Health and Care Excellence (NICE), UK Professor James Raftery Professor of Health Technology Assessment, Wessex Institute, Faculty of Medicine, University of Southampton, UK Dr Rob Riemsma Reviews Manager, Kleijnen Systematic Reviews Ltd, UK Professor Helen Roberts Professor of Child Health Research, UCL Institute of Child Health, UK Professor Helen Snooks Professor of Health Services Research, Institute of Life Science, College of Medicine, Swansea University, UK Professor Jim Thornton Professor of Obstetrics and Gynaecology, Faculty of Medicine and Health Sciences, University of Nottingham, UK Please visit the website for a list of members of the NIHR Journals Library Board: www.journalslibrary.nihr.ac.uk/about/editors Editorial contact: [email protected] NIHRJournalsLibrary www.journalslibrary.nihr.ac.uk DOI:10.3310/hta191010 HEALTHTECHNOLOGYASSESSMENT2015 VOL.19 NO.101 Abstract A randomised controlled trial of computerised cognitive behaviour therapy for the treatment of depression in primary care: the Randomised Evaluation of the Effectiveness and Acceptability of Computerised Therapy (REEACT) trial Elizabeth Littlewood,1 Ana Duarte,2 Catherine Hewitt,3 Sarah Knowles,4,5 Stephen Palmer,2 Simon Walker,2 Phil Andersen,1 Ricardo Araya,6,7 Michael Barkham,8 Peter Bower,5 Sally Brabyn,1 Gwen Brierley,1,9 Cindy Cooper,10 Linda Gask,5 David Kessler,11 Helen Lester,5,12† Karina Lovell,13 Usman Muhammad,3 Glenys Parry,10 David A Richards,1,14 Rachel Richardson,1 Debbie Tallon,15 Puvan Tharmanathan,3 David White10 and Simon Gilbody1* on behalf of the REEACT Team 1Department of HealthSciences, University of York, York, UK 2Centre forHealth Economics, University ofYork, York, UK 3YorkTrials Unit,Department ofHealth Sciences, University ofYork, York, UK 4Centre forPrimary Care, Institute ofPopulation Health, University ofManchester, Manchester, UK 5National Institute for HealthResearch (NIHR) School for PrimaryCare Research, Manchester Academic Health Science Centre,University ofManchester, Manchester, UK (previously National Primary CareResearch and Development Centre,University ofManchester, Manchester, UK) 6Academic Unit of Psychiatry, University ofBristol, Bristol, UK 7DepartmentofPopulationHealth,LondonSchoolofHygieneandTropicalMedicine,London,UK 8Centre forPsychological Services Research, University ofSheffield, Sheffield, UK 9Medical Research Council (MRC) Epidemiology Unit, University of Cambridge School ofClinical Medicine, Cambridge, UK 10Clinical Trials Research Unit, School ofHealth and Related Research, University of Sheffield, Sheffield, UK 11Academic Unit ofPrimary Health Care, University of Bristol, Bristol, UK 12Primary CareClinical Sciences, University ofBirmingham, Birmingham, UK 13School ofNursing, Midwifery and Social Work, University of Manchester, Manchester, UK 14University ofExeter Medical School, University ofExeter, Exeter, UK 15School ofSocial & Community Medicine, University ofBristol, Bristol, UK *Corresponding author [email protected] †In memoriam ©Queen’sPrinterandControllerofHMSO2015.ThisworkwasproducedbyLittlewoodetal.underthetermsofacommissioningcontractissuedbytheSecretaryofStatefor Health.Thisissuemaybefreelyreproducedforthepurposesofprivateresearchandstudyandextracts(orindeed,thefullreport)maybeincludedinprofessionaljournals vii providedthatsuitableacknowledgementismadeandthereproductionisnotassociatedwithanyformofadvertising.Applicationsforcommercialreproductionshouldbe addressedto:NIHRJournalsLibrary,NationalInstituteforHealthResearch,Evaluation,TrialsandStudiesCoordinatingCentre,AlphaHouse,UniversityofSouthamptonScience Park,SouthamptonSO167NS,UK. ABSTRACT Background: Computerised cognitive behaviour therapy (cCBT) hasbeen developed as anefficient form of therapy delivery with thepotential to enhance accessto psychological care. Independent research is needed which examines both the clinical effectiveness andcost-effectiveness of cCBT over theshort and longer term. Objectives: To compare the clinical effectiveness and cost-effectiveness of cCBT as anadjunct to usual general practitioner (GP) care againstusual GPcare alone,for afree-to-use cCBT program (MoodGYM; National Institute for Mental HealthResearch, Australian National University, Canberra, Australia) and a commercial pay-to-use cCBT program (Beating theBlues®; Ultrasis, London, UK) for adults with depression, and to determine the acceptability of cCBT and theexperiences of users. Design: A pragmatic, multicentre, three-armed, parallel, randomised controlled trial (RCT)with concurrent economic andqualitative evaluations. Simple randomisation was used.Participants and researchers were not blind to treatment allocation. Setting: Primary carein England. Participants: Adults with depression who scored ≥10 onthe Patient Health Questionnaire-9 (PHQ-9). Interventions: Participants whowere randomised to either of thetwo intervention groups receivedcCBT (Beating theBlues or MoodGYM) in additionto usualGP care. Participants whowere randomised to the control groupwere offered usualGP care. Main outcome measures: Theprimary outcome was depression at 4months (PHQ-9). Secondary outcomes were depression at 12 and 24 months; measures of mental health and health-related quality of life at 4, 12and 24 months; treatment preference; and theacceptability of cCBT and experiences of users. Results: Clinical effectiveness: 210 patients were randomised to Beating the Blues, 242 patients were randomised to MoodGYM and 239 patients were randomised to usual GP care(total 691).There was no difference in theprimary outcome (depression measured at 4months) either between Beating the Blues and usual GPcare [odds ratio (OR)1.19, 95% confidence interval (CI)0.75 to 1.88] or between MoodGYM and usualGP care (OR 0.98,95% CI 0.62 to 1.56). There was nooverall difference across all time points for either intervention compared with usualGP carein amixed model(Beating the Bluesversus usual GP care, p=0.96; and MoodGYMversus usualGP care, p=0.11). However, asmall but statistically significant difference between MoodGYM and usual GPcare at 12 months was found(OR 0.56, 95% CI 0.34 to 0.93). Free-to-use cCBT (MoodGYM) was notinferior to pay-to-use cCBT (Beating theBlues) (OR 0.91, 90% CI 0.62 to 1.34; p=0.69). There were no consistent benefits of either intervention when secondary outcomes were examined. There were noserious adverse events thoughtlikely to berelated to the trial intervention. Despite theprovision of regular technical telephone support, therewas low uptake of thecCBT programs. Cost-effectiveness: cost-effectiveness analyses suggest that neither Beating the Blues norMoodGYM appeared cost-effective comparedwith usual GP carealone.Qualitative evaluation: participants were often demotivated to accessthe computer programs, by reason of depression. Some expressed theview that agreater level of therapeutic input would beneeded to promote engagement. Conclusions: The benefits that have previously been observedin developer-led trials were not foundin this large pragmatic RCT. The benefits of cCBT when addedto routine primary care were minimal, and uptake of this mode of therapy was relatively low.There remains a clinical and economic need for effective low-intensity psychological treatments for depression with improved patient engagement. Trial registration: This trial isregistered as ISRCTN91947481. Funding: This project was funded bythe National Institute for Health Research Health Technology Assessment programme. viii NIHRJournalsLibrary www.journalslibrary.nihr.ac.uk

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Downloaded from: http://researchonline.lshtm.ac.uk/2478774/ .. TABLE 29 Participant response to the SF-6D questionnaire at each time point An additional GP practice incentive was the use of the Quality and Outcomes missing at random, conditional on the values of observed variables in the
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