Clinical trial Recruiting at 5 sites Phase 2 Interventional Ages 13 to 24

Comparing emergency care approaches for youth suicide prevention

Official title: Youth Partners in Care for Suicide Prevention

Run by University of California, Los Angeles · NCT05304065 · Data updated 2026-11-12

This study tests whether providing emergency care alone or adding follow-up support helps young people aged 13-24 who come to the hospital with suicidal thoughts feel better and stay engaged in mental health treatment.

Quick facts

PhasePhase 2
Study typeInterventional
Ages13 Years to 24 Years
SexAll
Enrollment1600 (estimated)
SponsorUniversity of California, Los Angeles
Academic / other
Locations5 sites (Los Angeles, California and 4 other locations)
StatusRecruiting
StartedOctober 17, 2022
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedDecember 31, 2025
Trial IDNCT05304065 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are youth aged 13-24 who have experienced suicidal behavior or ideation within the past week.

Probably not a fit

Patients with active psychosis, drug dependence, or those who cannot provide informed consent 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 trial evaluates two evidence-based interventions for youth aged 13-24 who present to the Emergency Department with suicidal thoughts or behaviors. It aims to determine the effectiveness of providing care solely in the ED versus a combined approach that includes aftercare follow-up. Participants will be monitored at baseline and through follow-up assessments at 3, 6, and 12 months to assess outcomes related to suicide attempts and mental health treatment engagement. The study addresses critical gaps in current knowledge about optimal intervention strategies for this vulnerable population.

Why it matters

Potential benefit: If successful, this study could lead to improved interventions that significantly reduce suicide attempts among youth.

How similar studies have gone: Previous studies have shown promise in similar interventions, but this specific comparison of ED and aftercare approaches is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* age 13-24;
* past-week suicidal behavior or ideation with plan or intent

Exclusion Criteria:

* symptoms or illness that precludes informed consent or engagement in study procedures (e.g., active psychosis; drug dependence, no locator information);
* youth not fluent in English
* parent not fluent in English or Spanish.

Where it's running

  • Ronald Reagan Medical Center
    Los Angeles, California, United States
    Recruiting
  • Olive View UCLA Education and Research Center
    Sylmar, California, United States
    Recruiting
  • Duke University
    Durham, North Carolina, United States
    Recruiting
  • Brown University
    Providence, Rhode Island, United States
    Recruiting
  • University of Utah
    Salt Lake City, Utah, United States
    Recruiting

Study contacts

  • Principal investigator: Joan R Asarnow, PhD — University of California, Los Angeles
  • Study coordinator: Lucas Zullo, PhD
  • Email: lzullo@mednet.ucla.edu
  • Phone: 310 794-4962

Similar studies

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

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  • Friends and family training for those at risk of suicide

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    Recruiting Unity Health Toronto · Toronto, Ontario · NCT07902089

  • Enhanced DBT skills group for Borderline Personality Disorder

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  • Blended ERITA for Teens Who Self-Injure

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    Recruiting Karolinska Institutet · Stockholm · NCT07755774

  • How people disclose suicidal thoughts and get support in rural eastern Uganda

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    Recruiting Yale University · Mpunde, Buyende District · NCT07730307

  • Reward Sensitivity Digital App for Adolescent Suicidal Thoughts

    A smartphone app is tested in teens to see if daily check-ins and mood-building activities can reduce suicidal thoughts and improve mood.

    Recruiting University of Pennsylvania · Philadelphia, Pennsylvania · NCT07661901

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.