Clinical trial Recruiting at 1 site Interventional Ages 13 to 18

A digital platform to reduce suicide risk in at-risk youth

Official title: Development and Testing of a Digitally Assisted Risk Reduction Platform for Youth at High Risk for Suicide

Run by Ksana Health · NCT05920252 · Data updated 2026-11-12

This study is testing a new digital platform called Vira to see if it can help reduce suicide risk in teens aged 13-18 who are getting treatment for mental health issues.

Quick facts

Study typeInterventional
Ages13 Years to 18 Years
SexAll
Enrollment78 (estimated)
SponsorKsana Health
Industry-sponsored
Locations1 site (New York, New York)
StatusRecruiting
StartedAugust 14, 2024
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedMarch 4, 2026
Trial IDNCT05920252 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adolescents aged 13-18 who are currently receiving treatment at the Intensive Adolescent and Family DBT Program and own a personal smartphone.

Probably not a fit

Patients who require a higher level of care or those already assigned a clinician in the program may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to address the rising rates of youth suicide by developing a digital platform called Vira, which integrates mobile sensing data and HIPAA-compliant communication tools for practitioners. The study will conduct a randomized controlled trial involving 200 adolescents aged 13-18 who are receiving treatment at the Intensive Adolescent and Family DBT Program. Participants will be divided into two groups: one using the Vira platform and the other receiving standard treatment. The goal is to evaluate whether the use of this digital platform improves clinical outcomes for youth at risk of suicide.

Why it matters

Potential benefit: If successful, this platform could significantly enhance the effectiveness of suicide prevention strategies for at-risk youth.

How similar studies have gone: Other studies have shown promise in using digital tools for mental health interventions, suggesting potential success for this novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Written informed assent from adolescents ages 13-17 years old and permission from legal guardians, or consent from adolescents age 18 years old.
* Receiving treatment at the Intensive Adolescent and Family DBT Pgogram
* 13-18 years old
* Owns a personal smartphone (Android or iPhone 7+)
* Fluent in English

Exclusion Criteria:

* Adolescents who require a higher level of care (i.e., are not admitted to the Intensive Outpatient DBT program)
* Adolescents who are receiving treatment at the Intensive Adolescent and Family DBT program and have already been assigned a clinician

Where it's running

  • Columbia University
    New York, New York, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.