跳至主要内容
临床试验/NCT05180344
NCT05180344招募中不适用

Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide

Butler Hospital1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年7月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
10
试验地点
1
主要终点
Acceptability of Research (Recruitment)

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
Non Randomized
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

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

研究组 & 干预措施

Mobile Application to Prevent Suicide (MAPS)

Experimental

Participants receiving MAPS will receive the Safety Planning Intervention (SPI) which will be uploaded into the smartphone app. They will be prompted four times per day to complete a brief ecological momentary assessment "check-in" inquiring about their cognitions, affect, and behavior, including suicidal thoughts and behaviors. Based on these responses, they will be provided with coping strategies from their safety plans and from a database of coping strategies created by study staff. They will also have access to emergency phone numbers, the coping strategies database, and can communicate with their study clinician through a text-like interface in the app. They will receive this intervention for one month.

干预措施: Mobile Application to Prevent Suicide (MAPS) (Behavioral)

结局指标

主要结局

Acceptability of Research (Recruitment)

时间窗: 1 month

Measured by dropout rate.

Acceptability of Research Procedures

时间窗: 1 month

Feedback on qualitative interview

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.

Acceptability of MAPS Intervention

时间窗: 1 month

Feedback on qualitative interview.

Satisfaction with MAPS Intervention

时间窗: 4 weeks

Measured by protocol completion rate.

Ecological Momentary Assessment (EMA) Adherence

时间窗: 4 weeks

Number of assessments completed out of total.

Acceptability of Research (Recruitment)

时间窗: Baseline

Measured by recruitment rate.

次要结局

  • Rehospitalization(1 month)
  • Suicidal Ideation and Behavior(1 month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验