NCT02313753已完成不适用
Evaluation of the Coping Long Term With Active Suicide Program
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 224
- 试验地点
- 1
- 主要终点
- A composite composed of the number of participants with either a suicide attempt or death by suicide
研究概览
简要总结
The purpose of this study is to evaluate the utility of the Coping Long Term with Active Suicide Program (CLASP) for reducing suicidal behavior.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Current patient at Butler Hospital
- •Suicide attempt or suicidal ideation with intent to make a suicide attempt within 48 hours of hospitalization as indicated on the hospital chart and confirmed by administration of the C-SSRS
- •Age > 18 years
- •Have a reliable telephone
- •Ability to speak, read, and understand English well to complete the procedures of the study
排除标准
- •Current psychotic symptoms severe enough to impair study participation
- •Participation in a treatment program with established efficacy in preventing suicidal behavior
- •Cognitive impairment which would interfere with adequate participation in the project (MMSE< 20).
- •Currently in state custody or pending legal action
- •Already enrolled current or previous CLASP trial
研究组 & 干预措施
SAFE
Active Comparator
Safety Assessment and Follow-up Evaluation Protocol
干预措施: SAFE (Behavioral)
CLASP
Experimental
Coping Long Term with Active Suicide Program Protocol
干预措施: CLASP (Behavioral)
结局指标
主要结局
A composite composed of the number of participants with either a suicide attempt or death by suicide
时间窗: 52 weeks following discharge from hospital
As assessed by both the Columbia Suicide Severity Rating Scale and record review
次要结局
未报告次要终点
研究者
Ivan Miller
Director, Psychosocial Research
Butler Hospital
研究点 (1)
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