A Digitally Assisted Risk Reduction Platform for Youth at High Risk for Suicide (NCT05920252)
Development and Testing of a Digitally Assisted Risk Reduction Platform for Youth at High Risk for Suicide
๐ฉบ Plain-English Summary (8th-Grade Level)
Despite efforts to prevent suicide, US rates are climbing, and suicide is the second leading cause of death among youth. Digital tools, especially personal smartphones, are promising avenues to address these issues and can be used to provide a unique understanding of risk factors, including psychological distress, anhedonia and behavioral withdrawal, and sleep disturbance among high-risk individuals. This project aims to enhance the effectiveness of the delivery of preventative health care to youth at risk for suicide by developing a comprehensive digital platform that allows practitioners to integrate mobile sensing data and HIPAA-compliant client communication tools into their management of these young people.
Who can join: Review the eligibility criteria below.
Location: Columbia University โ New York, New York
Age range: 13 Years to 18 Years
๐งช Interventions in This Study
- Vira (BEHAVIORAL)
- Treatment as Usual (TAU) (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Columbia University โ New York, New York
๐ Contact the Study Coordinator
Phone: (646) 774-5745
Email: rpa2009@cumc.columbia.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Suicide
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- Wearable Suicidal Early Warning System for Adolescents โ Portland, Oregon
- Comparing Suicide Prevention Interventions to Guide Follow-up Care: The SPRING Trial โ Boise, Idaho
- Suicide Prevention for Sexual and Gender Minority Youth (Randomized Controlled Trial) โ San Diego, California
- Scaling Out S.A.F.E. Firearm Across Two Health Systems as a Universal Suicide Prevention Strategy (SCALE ASPIRE) โ Aurora, Colorado
- Rapid Personalization of Safety Plans for Psychiatrically Hospitalized Veterans at High-Risk for Suicide โ Boston, Massachusetts
Explore by condition: All Suicide clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.