Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Ecological Momentary Assessment (EMA) Adherence
研究概览
简要总结
The primary aim of this grant is to conduct pilot testing on a novel personalized mobile intervention for suicide - Mobile Application to Prevent Suicide (MAPS) - and to establish feasibility, acceptability, safety, and primary outcomes (i.e., suicidal ideation and behavior; re-hospitalization).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 26 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Suicidal ideation and/or suicidal behavior in the past month verified by the C-SSRS
- •Between the ages of 18 and 26
- •English proficiency
- •Comfortable with smartphone technology
- •Deemed by the treatment team to be stable enough to complete study procedures
排除标准
- •Current psychotic or manic symptoms severe enough to interfere with study procedures
结局指标
主要结局
Ecological Momentary Assessment (EMA) Adherence
时间窗: 4 weeks
Number of assessments completed out of total.
Acceptability of Research Procedures
时间窗: 1 month
Feedback on qualitative interview
Acceptability of MAPS Intervention
时间窗: 1 month
Feedback on qualitative interview.
Acceptability of Research (Recruitment)
时间窗: Baseline
Measured by recruitment rate.
Acceptability of Research (Dropout)
时间窗: 1 month
Measured by dropout rate.
Patient Satisfaction
时间窗: 1 month
Measured using the Client Satisfaction Questionnaire, a self-report measure of satisfaction with treatment. Scores range from 8 to 32, with higher scores representing higher satisfaction.
Satisfaction with MAPS Intervention
时间窗: 4 weeks
Measured by protocol completion rate.
次要结局
- Rehospitalization(1 month)
- Suicidal Ideation and Behavior(1 month)