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Structured Psychological Support for people with personality disorder: feasibility randomised controlled trial of a low-intensity intervention
被引:13
|作者:
Crawford, Mike J.
[1
]
Thana, Lavanya
[2
]
Parker, Jennie
[2
]
Turner, Oliver
[3
]
Carney, Aidan
[4
]
McMurran, Mary
[5
]
Moran, Paul
[6
]
Weaver, Timothy
[7
]
Barrett, Barbara
[8
]
Roberts, Sarah
[8
]
Claringbold, Amy
[1
]
Bassett, Paul
[9
]
Sanatinia, Rahil
[1
]
Spong, Amanda
[10
]
机构:
[1] Imperial Coll London, Div Psychiat, London, England
[2] Cent & North West London NHS Fdn Trust, Res & Dev, London, England
[3] Barnet Enfield & Haringey NHS Trust, Div Specialist Serv, Enfield, Middx, England
[4] Cent & North West London NHS Fdn Trust, Adult Mental Hlth Directorate, London, England
[5] Univ Nottingham, Psychiat & Appl Psychol Dept, Nottingham, England
[6] Univ Bristol, Ctr Acad Mental Hlth, Bristol, Avon, England
[7] Middlesex Univ, Sch Hlth & Educ, London, England
[8] Kings Coll London, Hlth Serv & Populat Res, London, England
[9] Statsconsultancy Ltd, Amersham, England
[10] Cambridgeshire & Peterborough NHS Fdn Trust, Clin Psychol, Cambridge, England
来源:
基金:
美国国家卫生研究院;
关键词:
Personality disorder;
psychological treatment;
low intensity;
brief intervention;
randomised trial;
DIALECTICAL BEHAVIOR-THERAPY;
DELIBERATE SELF-HARM;
CARE;
PREVALENCE;
WOMEN;
D O I:
10.1192/bjo.2020.7
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Background National guidance cautions against low-intensity interventions for people with personality disorder, but evidence from trials is lacking. Aims To test the feasibility of conducting a randomised trial of a low-intensity intervention for people with personality disorder. Method Single-blind, feasibility trial (trial registration: ISRCTN14994755). We recruited people aged 18 or over with a clinical diagnosis of personality disorder from mental health services, excluding those with a coexisting organic or psychotic mental disorder. We randomly allocated participants via a remote system on a 1:1 ratio to six to ten sessions of Structured Psychological Support (SPS) or to treatment as usual. We assessed social functioning, mental health, health-related quality of life, satisfaction with care and resource use and costs at baseline and 24 weeks after randomisation. Results A total of 63 participants were randomly assigned to either SPS (n = 33) or treatment as usual (n = 30). Twenty-nine (88%) of those in the active arm of the trial received one or more session (median 7). Among 46 (73%) who were followed up at 24 weeks, social dysfunction was lower (-6.3, 95% CI -12.0 to -0.6, P = 0.03) and satisfaction with care was higher (6.5, 95% CI 2.5 to 10.4; P = 0.002) in those allocated to SPS. Statistically significant differences were not found in other outcomes. The cost of the intervention was low and total costs over 24 weeks were similar in both groups. Conclusions SPS may provide an effective low-intensity intervention for people with personality disorder and should be tested in fully powered clinical trials.
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