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临床试验/NCT06349915
NCT06349915招募中不适用

A Pilot Evaluation of a Digital Peer Support Intervention for Suicidal Adolescents

Albert Einstein College of Medicine1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2026年8月1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
46
试验地点
1
主要终点
Suicidal Thoughts

研究概览

简要总结

Suicide risk has increased among youth in underserved communities, where access to mental healthcare is limited. To address this need, the investigator team plans to evaluate the preliminary efficacy of a brief, low-cost, culturally responsive digital intervention for ethnically diverse youth at risk for suicide in The Bronx, New York. In collaboration with community stakeholders, suicide recovery narratives, featuring adolescents' experiences related to recovery from suicidal thoughts will be developed. A smartphone ecological momentary assessment (EMA) app will be used to evaluate whether a curriculum of these narratives provides anti-suicidal benefits to at-risk adolescents.

详细描述

This is a single-arm investigation of a novel suicide prevention intervention, called "Supporting Wellbeing with Everyday Experiences of Peers" (SWEEP). In a preliminary phase (Phase 1) of the study, suicide recovery narratives: short first-person stories about lived experience with and recovery from Bronx Adolescents will be collected. The investigator team will then evaluate evaluate the anti-suicidal benefits of this intervention in a single-arm trial. In a subsequent phase (Phase 2), adolescent participants (n=46) will be provided with the SWEEP intervention, which involves reading or listening to one suicide recovery narrative each day during the 14-day trial. Six of the 46 participants will be adolescents, with recent suicidal thoughts or depression, who are currently receiving mental healthcare in Montefiore's Outpatient Psychiatry Department, rather than those on the waitlist to receive these services. All six participants will then complete a post-intervention qualitative interview to inform potential changes to intervention procedures. During this second phase, suicide recovery narratives will be provided, in audio and text formats, via a smartphone app. That same smartphone app will also collect real-time (ecological momentary) assessments of suicidal thoughts, as well as secondary and additional outcomes, five times per day. The investigator team will evaluate whether participants experience reductions in the intensity of suicidal thoughts over the course of the 14-day trial. During Phase 3, participants will be recruited to a control condition (n=15) and a treatment condition (n=30). Those in the Phase 3 treatment condition will receive the same intervention (1 SWEEP narrative per day for 14 days + 3x/day EMA) as those in Phase 2. Those in the Control condition will receive 3x/day EMA only.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
14 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • past-month history of suicidal thoughts
  • past-month history of Major depressive disorder
  • possession of apple or android smartphone with data plan

排除标准

  • inability to read/write in English
  • Active mania
  • Active psychosis
  • Autism spectrum disorder

研究组 & 干预措施

Intervention

Experimental

This is a single-arm study. All participants will be allocated to the intervention arm, in which they will receive the digital narrative therapy.

干预措施: Supporting Wellbeing with Everyday Experiences of Peers (SWEEP) (Behavioral)

结局指标

主要结局

Suicidal Thoughts

时间窗: 5 times per day during 14-day trial

Participants will self-report their current subjective intensity of suicidal thoughts using an 11-point Likert-type scale, with higher scores indicating more intense suicidal thoughts.

次要结局

  • Suicidal Urge Resistance(5 times per day during 14-day trial)
  • Optimism(5 times per day during 14-day trial)
  • Social Support(5 times per day during 14-day trial)
  • Intervention Acceptability(Study conclusion (at the end of the 14-day trial))
  • Social Connectedness(5 times per day during 14-day trial)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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