跳至主要内容
临床试验/NCT06701006
NCT06701006招募中不适用

Integrated Screening and Safety Planning (ISSP) for Adolescents With Suicidal Thoughts

University of Washington2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年8月19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
60
试验地点
2
主要终点
Youth Suicide-Related Coping

研究概览

简要总结

The goal of this clinical trial is to evaluate an app to help keep teens and young adults with suicidal thoughts safe. The app includes a safety plan created by adolescents and healthcare providers, and videos to encourage supportive communication and skills for teens and young adults to stay safe. The main question it aims to answer is whether the use of an app can increase youth suicide-related coping for youth with suicidal ideation, parent/caregiver suicide prevention self-efficacy, and healthcare provider self-efficacy in suicide management. Researchers will compare usual care to usual care with the app. Participants, including adolescents, caregivers, and healthcare providers, will use the ISSP app (if assigned to that group) and view video content and complete three online surveys.

详细描述

The current study aims to evaluate the Jaspr app relative to usual care among youth (ages 13-21 years) who indicate suicidal ideation in pediatric medical settings. The Jaspr app includes supported safety planning between the young person and the healthcare provider, as well as skills and support videos for youth and caregivers intended to increase coping and decrease distress with an opportunity to access these resources through an at home app. Adolescents, parents, and clinicians will participate in the project to assess the effectiveness of Jaspr augmenting usual care, compared to usual care alone. The study will use a pre-post design in which each setting begins with a control period and then transitions to the addition of Jaspr following healthcare provider training on use of the app. Participants and their parents/caregivers will receive study assessments at baseline, 1-month, and 2-month follow up timepoints, and healthcare providers complete a survey at baseline, and the end of each period (control and intervention). Study assessments with youth will ask about coping, suicidal ideation and severity, anxiety and depression, service utilization, functional impairment, access to lethal means, and acceptability of the app. Study assessments for parents/caregivers will ask about their self-efficacy in managing their youth's suicidality, acceptability of the videos/app, and service utilization for the youth. Healthcare providers will complete surveys assessing their self-efficacy in managing youth suicidality and feasibility of use of the app. Youth, their legal guardian, and healthcare providers each assent/consent to participate in the research procedures.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
13 Years 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Youth Inclusion Criteria:
  • Age 13 -21 years, an Ask Suicide Questions (ASQ) screen score of 1-5 with active ideation (not solely a history of a prior attempt) but no current plan or intent, or patient-reported suicidal thoughts and behaviors during a clinical assessment in a medical setting who are judged by a clinician to be appropriate for conducting higher level assessment in that setting (including a BSSA and/or safety planning) in order to support care at home.
  • Parents/guardians: One "parent" per AYA will also be invited to participate.
  • HCPs: All HCPs in participating settings who may conduct assessments of SI and safety planning (physicians, nurse practitioners/physician's assistants, social workers, mental health counselors, psychologists) will be invited to participate.
  • All subjects must have access to the internet and a computer or tablet device.

排除标准

  • Concurrently enrolled in an affiliated Suicide Care Research Center study, no phone access, or non-English speaking.

研究组 & 干预措施

Usual Care

No Intervention

Integrated skills and safety planning app

Experimental

Use of Jaspr app for clinical care + at home

干预措施: Integrated skills and safety planning app (Other)

结局指标

主要结局

Youth Suicide-Related Coping

时间窗: Baseline, 1 month, 2 month

Total Score on the 17-item Youth Suicide-Related Coping Scale

Parent suicide prevention self-efficacy

时间窗: Baseline, 1 month, 2 month

Total score on the Parent suicide prevention self-efficacy scale

Healthcare provider self-efficacy in suicide management

时间窗: Baseline, end of control period, and end of intervention period

Total score on the Provider suicide Intervention Questionnaire

次要结局

  • Safety Plan Quality(Up to 1 month)
  • Youth Suicide Severity(Baseline, 1 month, 2 month)
  • Youth Anxiety Symptoms(Baseline, 1 month, 2 month)
  • Intervention Acceptability(Baseline, 1 month, 2 month)
  • Functional Impairment(Baseline, 1 month, 2 month)
  • Youth Suicidal ideation(Baseline, 1 month, 2 month)
  • Youth Depressive Symptoms(Baseline, 1 month, 2 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Laura Richardson

Professor of Pediatrics

University of Washington

研究点 (2)

Loading locations...

相似试验

Integrated Suicide Supports and Safety Planning for... | 临床试验