The DiaS trial: dialectical behavior therapy versus collaborative assessment and management of suicidality on self-harm in patients with a recent suicide attempt and borderline personality disorder traits - study protocol for a randomized controlled trial

被引:8
作者
Andreasson, Kate [1 ,6 ]
Krogh, Jesper [1 ]
Rosenbaum, Bent [2 ,3 ]
Gluud, Christian [4 ]
Jobes, David A. [5 ]
Nordentoft, Merete [1 ]
机构
[1] Univ Copenhagen, Fac Hlth Sci, Mental Hlth Ctr Copenhagen, Copenhagen, Denmark
[2] Mental Hlth Serv, iPSYCH, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark
[4] Copenhagen Univ Hosp, Rigshosp, Ctr Clin Intervent Res, Copenhagen Trial Unit, DK-2100 Copenhagen, Denmark
[5] Catholic Univ Amer, Dept Psychol, Washington, DC 20064 USA
[6] Mental Hlth Ctr, Res Unit, iPSYCH, DK-2400 Copenhagen NV, Denmark
关键词
suicide prevention; deliberate self-harm; borderline personality disorder traits; BPD; dialectical behavior therapy; DBT; collaborative assessment and management of suicidality; CAMS; RATING-SCALE; DSM-IV; IMPULSIVENESS; INTERVIEW; CAMS;
D O I
10.1186/1745-6215-15-194
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: In Denmark 8,000 to 10,000 people will attempt suicide each year. The Centre of Excellence in Suicide Prevention in the Capital Region of Denmark is treating patients with suicidal behavior, and a recent survey has shown that 30% of the patients are suffering from borderline personality disorder. The majority of patients (70% to 75%) with borderline personality disorder have a history of deliberate self-harm and 10% have a lifetime risk to die by suicide. The DiaS trial is comparing dialectical behavior therapy with collaborative assessment and management of suicidality-informed supportive psychotherapy, for the risk of repetition of deliberate self-harm in patients with a recent suicide attempt and personality traits within the spectrum of borderline personality disorder. Both treatments have previously shown effects in this group of patients on suicide ideation and self-harm compared with treatment as usual. Methods/Design: The trial is designed as a single-center, two-armed, parallel-group observer-blinded randomized clinical superiority trial. We will recruit 160 participants with a recent suicide attempt and at least two traits of the borderline personality disorder from the Centre of Excellence in Suicide Prevention, Capital Region of Denmark. Randomization will be performed though a centralized and computer-generated approach that conceals the randomization sequence. The interventions that are offered are a modified version of a dialectical behavior therapy program lasting 16 weeks versus collaborative assessment and management of suicidality-informed supportive psychotherapy, where the duration treatment will vary in accordance with established methods up to 16 weeks. The primary outcome measure is the ratio of deliberate self-harming acts including suicide attempts measured at week 28. Other exploratory outcomes are included such as severity of symptoms, suicide intention and ideation, depression, hopelessness, self-esteem, impulsivity, anger, and duration of respective treatments.
引用
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页数:8
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