Clinical effectiveness and cost-effectiveness of Structured Psychological Support for people with probable personality disorder in mental health services in England: study protocol for a randomised controlled trial

被引:0
|
作者
Crawford, Mike J. [1 ]
Leeson, Verity C. [1 ]
Evans, Rachel [2 ]
Goulden, Nia [2 ]
Weaver, Tim [3 ]
Trumm, Aile [3 ]
Barrett, Barbara M. [4 ]
Khun-Thompson, Fiona [5 ]
Pandya, Snehal P. [1 ]
Saunders, Kate E. [6 ]
Lamph, Gary [7 ]
Woods, David [8 ]
Smith, Harriet [9 ]
Greenall, Toby [10 ]
Nicklin, Victoria [11 ]
Barnicot, Kirsten [12 ]
机构
[1] Imperial Coll London, London, England
[2] Bangor Univ, Bangor, Gwynedd, Wales
[3] Middlesex Univ, Dept Mental Hlth & Social Work, London, England
[4] Kings Coll London, London, England
[5] Cent & North West London NHS Fdn Trust, London, England
[6] Warneford Hosp, Dept Psychiat, Oxford, England
[7] Keele Univ, Sch Nursing & Midwifery, Keele, Staffs, England
[8] Derbyshire Healthcare NHS Fdn Trust, Derby, England
[9] Avon & Wiltshire Mental Hlth Partnership NHS Trus, Bath, Avon, England
[10] Lincolnshire Community Hlth Serv NHS Trust, Lincoln, England
[11] Coventry & Warwickshire Partnership NHS Trust, Coventry, W Midlands, England
[12] City Univ London, London, England
来源
BMJ OPEN | 2024年 / 14卷 / 06期
关键词
Personality disorders; MENTAL HEALTH; Randomized Controlled Trial; Psychosocial Intervention; ATOPIC-DERMATITIS; CHILDREN; ECZEMA; ADHD;
D O I
10.1136/bmjopen-2024-086593
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Evidence-based psychological treatments for people with personality disorder usually involve attending group-based sessions over many months. Low-intensity psychological interventions of less than 6months duration have been developed, but their clinical effectiveness and cost-effectiveness are unclear. Methods and analysis This is a multicentre, randomised, parallel-group, researcher-masked, superiority trial. Study participants will be aged 18 and over, have probable personality disorder and be treated by mental health staff in seven centres in England. We will exclude people who are: unwilling or unable to provide written informed consent, have a coexisting organic or psychotic mental disorder, or are already receiving psychological treatment for personality disorder or on a waiting list for such treatment. In the intervention group, participants will be offered up to 10 individual sessions of Structured Psychological Support. In the control group, participants will be offered treatment as usual plus a single session of personalised crisis planning. The primary outcome is social functioning measured over 12 months using total score on the Work and Social Adjustment Scale (WSAS). Secondary outcomes include mental health, suicidal behaviour, health-related quality of life, patient-rated global improvement and satisfaction, and resource use and costs. The primary analysis will compare WSAS scores across the 12-month period using a general linear mixed model adjusting for baseline scores, allocation group and study centre on an intention-to-treat basis. In a parallel process evaluation, we will analyse qualitative data from interviews with study participants, clinical staff and researchers to examine mechanisms of impact and contextual factors. Ethics and dissemination The study complies with the Helsinki Declaration II and is approved by the London-Bromley Research Ethics Committee (IRAS ID 315951). Study findings will be published in an open access peer-reviewed journal; and disseminated at national and international conferences. Trial registration number ISRCTN13918289.
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页数:9
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