Refractory depression - mechanisms and efficacy of radically open dialectical behaviour therapy (RefraMED): findings of a randomised trial on benefits and harms.


Journal

The British journal of psychiatry : the journal of mental science
ISSN: 1472-1465
Titre abrégé: Br J Psychiatry
Pays: England
ID NLM: 0342367

Informations de publication

Date de publication:
04 2020
Historique:
pubmed: 19 7 2019
medline: 5 1 2021
entrez: 19 7 2019
Statut: ppublish

Résumé

Individuals with depression often do not respond to medication or psychotherapy. Radically open dialectical behaviour therapy (RO DBT) is a new treatment targeting overcontrolled personality, common in refractory depression. To compare RO DBT plus treatment as usual (TAU) for refractory depression with TAU alone (trial registration: ISRCTN 85784627). RO DBT comprised 29 therapy sessions and 27 skills classes over 6 months. Our completed randomised trial evaluated RO DBT for refractory depression over 18 months in three British secondary care centres. Of 250 adult participants, we randomised 162 (65%) to RO DBT. The primary outcome was the Hamilton Rating Scale for Depression (HRSD), assessed masked and analysed by treatment allocated. After 7 months, immediately following therapy, RO DBT had significantly reduced depressive symptoms by 5.40 points on the HRSD relative to TAU (95% CI 0.94-9.85). After 12 months (primary end-point), the difference of 2.15 points on the HRSD in favour of RO DBT was not significant (95% CI -2.28 to 6.59); nor was that of 1.69 points on the HRSD at 18 months (95% CI -2.84 to 6.22). Throughout RO DBT participants reported significantly better psychological flexibility and emotional coping than controls. However, they reported eight possible serious adverse reactions compared with none in the control group. The RO DBT group reported significantly lower HRSD scores than the control group after 7 months, but not thereafter. The imbalance in serious adverse reactions was probably because of the controls' limited opportunities to report these.

Sections du résumé

BACKGROUND
Individuals with depression often do not respond to medication or psychotherapy. Radically open dialectical behaviour therapy (RO DBT) is a new treatment targeting overcontrolled personality, common in refractory depression.
AIMS
To compare RO DBT plus treatment as usual (TAU) for refractory depression with TAU alone (trial registration: ISRCTN 85784627).
METHOD
RO DBT comprised 29 therapy sessions and 27 skills classes over 6 months. Our completed randomised trial evaluated RO DBT for refractory depression over 18 months in three British secondary care centres. Of 250 adult participants, we randomised 162 (65%) to RO DBT. The primary outcome was the Hamilton Rating Scale for Depression (HRSD), assessed masked and analysed by treatment allocated.
RESULTS
After 7 months, immediately following therapy, RO DBT had significantly reduced depressive symptoms by 5.40 points on the HRSD relative to TAU (95% CI 0.94-9.85). After 12 months (primary end-point), the difference of 2.15 points on the HRSD in favour of RO DBT was not significant (95% CI -2.28 to 6.59); nor was that of 1.69 points on the HRSD at 18 months (95% CI -2.84 to 6.22). Throughout RO DBT participants reported significantly better psychological flexibility and emotional coping than controls. However, they reported eight possible serious adverse reactions compared with none in the control group.
CONCLUSIONS
The RO DBT group reported significantly lower HRSD scores than the control group after 7 months, but not thereafter. The imbalance in serious adverse reactions was probably because of the controls' limited opportunities to report these.

Identifiants

pubmed: 31317843
pii: S0007125019000539
doi: 10.1192/bjp.2019.53
pmc: PMC7282863
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

204-212

Subventions

Organisme : Medical Research Council
Pays : United Kingdom

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Auteurs

Thomas R Lynch (TR)

Emeritus Professor of Clinical Psychology, Department of Psychology, University of Southampton, UK.

Roelie J Hempel (RJ)

Senior Research Fellow, Department of Psychology, University of Southampton, UK.

Ben Whalley (B)

Lecturer in Psychology, Cognition Institute, School of Psychology, Plymouth University, UK.

Sarah Byford (S)

Professor of Health Economics, Institute of Psychiatry, Psychology & Neuroscience, King's College London, UK.

Rampaul Chamba (R)

Patient and Public Representative, Member of Trial Management Committee responsible for Public & Patient Inclusion, UK.

Paul Clarke (P)

Professor of Social Statistics, Institute for Social and Economic Research, University of Essex, UK.

Susan Clarke (S)

Visiting Professor, Consultant Clinical Psychologist, Intensive Psychological Therapies Service, Dorset Healthcare University NHS Foundation Trust, UK.

David G Kingdon (DG)

Professor of Mental Health Care Delivery, Department of Medicine, University of Southampton, UK.

Heather O'Mahen (H)

Senior Lecturer in Clinical Psychology, Department of Psychology, College of Life and Environmental Sciences, University of Exeter, UK.

Bob Remington (B)

Emeritus Professor in Psychology, Department of Psychology, University of Southampton, UK.

Sophie C Rushbrook (SC)

Consultant Clinical Psychologist, Intensive Psychological Therapies Service, Dorset Healthcare University NHS Foundation Trust, UK.

James Shearer (J)

Lecturer in Health Economics, Institute of Psychiatry, Psychology & Neuroscience, King's College London, UK.

Maggie Stanton (M)

Consultant Clinical Psychologist, Psychological Services, Southern Health NHS Foundation Trust, UK.

Michaela Swales (M)

Consultant Clinical Psychologist and Reader in Clinical Psychology, School of Psychology, Bangor University, UK.

Alan Watkins (A)

Associate Professor of e-Trials Research, Medical School, Swansea University, UK.

Ian T Russell (IT)

Professor of Clinical Trials, Medical School, Swansea University, UK.

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