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dc.contributor.authorKuyken, W
dc.contributor.authorByford, S
dc.contributor.authorByng, R
dc.contributor.authorDalgleish, T
dc.contributor.authorLewis, G
dc.contributor.authorTaylor, R
dc.contributor.authorWatkins, ER
dc.contributor.authorHayes, R
dc.contributor.authorLanham, P
dc.contributor.authorKessler, D
dc.contributor.authorMorant, N
dc.contributor.authorEvans, A
dc.date.accessioned2017-01-24T12:42:59Z
dc.date.issued2014-06-10
dc.description.abstractBACKGROUND: Depression is a common and distressing mental health problem that is responsible for significant individual disability and cost to society. Medication and psychological therapies are effective for treating depression and maintenance anti-depressants (m-ADM) can prevent relapse. However, individuals with depression often express a wish for psychological help that can help them recover from depression in the long-term. A recently developed treatment, mindfulness-based cognitive therapy (MBCT), shows potential as a brief group program for people with recurring depression.This trial asks the policy research question; is MBCT with support to taper/discontinue antidepressant medication (MBCT-TS) superior to m-ADM in terms of: a primary outcome of preventing depressive relapse/recurrence over 24 months; and secondary outcomes of (a) depression free days, (b) residual depressive symptoms, (c) antidepressant medication (ADM) usage, (d) psychiatric and medical co-morbidity, (e) quality of life, and (f) cost effectiveness? An explanatory research question also asks whether an increase in mindfulness skills is the key mechanism of change.The design is a single-blind, parallel randomized controlled trial examining MBCT-TS versus m-ADM with an embedded process study. To answer the main policy research question the proposed trial compares MBCT-TS with m-ADM for patients with recurrent depression. Four hundred and twenty patients with recurrent major depressive disorder in full or partial remission will be recruited through primary care. RESULTS: Depressive relapse/recurrence over two years is the primary outcome variable. Analyses will be conducted following CONSORT standards and overseen by the trial's Data Monitoring and Safety Committee. Initial analyses will be conducted on an intention-to-treat basis, with subsequent analyses being per protocol. The explanatory question will be addressed in two mutually informative ways: quantitative measurement of potential mediating variables pre- and post-treatment and a qualitative study of service users' views and experiences. CONCLUSIONS: If the results of our exploratory trial are extended to this definitive trial, MBCT-TS will be established as an alternative approach to maintenance antidepressants for people with a history of recurrent depression. The process studies will provide evidence about the effective components which can be used to improve MBCT and inform theory as well as other therapeutic approaches. TRIAL REGISTRATION: Trial registered 7 May 2009; ISRCTN26666654.en_GB
dc.description.sponsorshipThis research is funded by the National Institutes of Health Research Health Technology Assessment Program in the UK, grant number 08/56/01. The lead author is supported in part by the NIHR PenCLAHRC. The study has support from the UK Mental Health Research Network, the Comprehensive Local Research Network and the Primary Care Research Network. We are grateful to Trish Bartley at the University of Bangor Centre for Mindfulness Research and Practice for her input to the MBCT therapist training; the independent members of the Trial Steering Committee (Prof Chris Leach, Chair, Dr Richard Moore and Prof Glenys Parry); and the independent members of the Data Monitoring Committee (Dr Paul Ewings, Chair, Dr Andy Field and Dr Joanna McKenzie). The trial team comprises: Surinder Kaur, Jon Richards, Alice Weaver and Matt Williams (research staff), Claire Brejcha, Suzanne Cowderoy, Alison Evans and Jenny Wilks (MBCT therapists), Harry Sutton (administrator), Cara Simmance and Liz Upward provided voluntary research assistance.en_GB
dc.identifier.citationVol. 15: 217en_GB
dc.identifier.doi10.1186/1745-6215-15-217
dc.identifier.other1745-6215-15-217
dc.identifier.urihttp://hdl.handle.net/10871/25381
dc.language.isoenen_GB
dc.publisherBioMed Centralen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/24916319en_GB
dc.rights© 2014 Kuyken et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_GB
dc.subjectAntidepressive Agentsen_GB
dc.subjectClinical Governanceen_GB
dc.subjectCognitive Therapyen_GB
dc.subjectDepressive Disorder, Majoren_GB
dc.subjectHumansen_GB
dc.subjectMindfulnessen_GB
dc.subjectResearch Designen_GB
dc.subjectSecondary Preventionen_GB
dc.subjectSubstance Withdrawal Syndromeen_GB
dc.titleUpdate to the study protocol for a randomized controlled trial comparing mindfulness-based cognitive therapy with maintenance anti-depressant treatment depressive relapse/recurrence: the PREVENT trial.en_GB
dc.typeArticleen_GB
dc.date.available2017-01-24T12:42:59Z
dc.identifier.issn1745-6215
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the final version of the article. Available from the publisher via the DOI in this record.en_GB
dc.identifier.journalTrialsen_GB
dc.identifier.pmcidPMC4066271
dc.identifier.pmid24916319


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