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Youth Partners in Care for Suicide Prevention

About

Brief Summary

This randomized comparative effectiveness trial will compare two evidence-based approaches to emergency care for youth ages 15-24 who present to the Emergency Department (ED) with suicidal ideation or behavior. OUtcomes will be monitored at baseline and at 3, 6 & 12 month follow-up assessments.

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase II

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
15 Years
Maximum Age
24 Years

Inclusion Criteria:

  • age 15-24;
  • 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.

Join this Trial

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Study Stats
Protocol No.
22-000461
Category
Mental Health
Pediatric and Prenatal Disorders
Contact
Lucas Zullo
Location
  • UCLA Westwood
For Providers
NCT No.
NCT05304065
For detailed technical eligibility, visit ClinicalTrials.gov.