Recruiting

ISSP App

Sponsor:

University of Washington

Code:

NCT06701006

Conditions

Suicidal Ideation

Suicidal Behavior

Eligibility Criteria

Sex: All

Age: 13 - 21

Healthy Volunteers: Not accepted

Interventions

Integrated skills and safety planning app

Study Details

Brief summary:

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.

Conditions

Suicidal Ideation

Suicidal Behavior

Study ID

NCT06701006

Start date

Aug 19, 2025

Status verified date

Nov, 2025

Completion date

Nov 1, 2026

Anticipated

Primary completion date

Nov 1, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 13 - 21

Healthy Volunteers: Not accepted

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.

Youth Exclusion Criteria:

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

Study Design

Enrollment

60 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

no intervention: Usual Care

experimental: Integrated skills and safety planning app

Use of Jaspr app for clinical care + at home

Interventions

Integrated skills and safety planning app

This is a digital app that includes supported safety planning resources in medical settings as well as coping skills and lived experience videos for adolescents, young adults and parents/caregivers that can be accessed while in the medical setting or at home.

Primary outcome measure

  • Youth Suicide-Related Coping [ Time Frame: Baseline, 1 month, 2 month ]
  • Parent suicide prevention self-efficacy [ Time Frame: Baseline, 1 month, 2 month ]
  • Healthcare provider self-efficacy in suicide management [ Time Frame: Baseline, end of control period, and end of intervention period ]

Central Contacts and Locations

Central contacts

Laura Richardson, MD, MPH

206-987-2028lpr@uw.edu

Locations

Seattle Children's Hospital

Recruiting

Seattle, Washington, United States, 98115

Contacts

Principal Investigator:

Laura Richardson, MD MPH

More Information

Sponsor

University of Washington

Last update posted

May 18, 2026

Last verified

Nov, 2025

Keywords

  • adolescents
  • young adults
  • suicide prevention
  • health services research

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Washington on 2026-05-18.