NCT06701006 Integrated Suicide Supports and Safety Planning for Youth
| NCT ID | NCT06701006 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Washington |
| Condition | Suicidal Ideation |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-08-19 |
| Primary Completion | 2026-11-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2025-08-19 with a primary completion date of 2026-11-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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.
Eligibility Criteria
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.
Contact & Investigator
Laura Richardson, MD, MPH
PRINCIPAL INVESTIGATOR
University of Washington
Frequently Asked Questions
Who can join the NCT06701006 clinical trial?
This trial is open to participants of all sexes, aged 13 Years or older, up to 21 Years, studying Suicidal Ideation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06701006 currently recruiting?
Yes, NCT06701006 is actively recruiting participants. Contact the research team at lpr@uw.edu for enrollment information.
Where is the NCT06701006 trial being conducted?
This trial is being conducted at Seattle, United States.
Who is sponsoring the NCT06701006 clinical trial?
NCT06701006 is sponsored by University of Washington. The principal investigator is Laura Richardson, MD, MPH at University of Washington. The trial plans to enroll 60 participants.