Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care
NCT05869552
This study is recruiting at 3 US sites in 2 states, according to its ClinicalTrials.gov record last updated .
Summary
The overall aim of this study is to reduce suicide among sexual and gender diverse youth ages 18-24 years old. This study will compare the effectiveness of two brief suicide prevention interventions that have been adapted for use with this population to use in primary care via telehealth and will recruit youth from primary care clinics in multiple metropolitan areas. The primary study outcome is suicidal ideation. Each clinic will be randomly assigned to deliver one of the two study interventions.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Suicide
- Suicidal Ideation
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 to 24 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Elizabeth Arnold
- Last updated on ClinicalTrials.gov
- November 6, 2025
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Pennsylvania · 1
- University of Pittsburgh · Pittsburgh, PA
Texas · 2
- Steve Hicks School of Social Work at the University of Texas at Austin · Austin, TX
- University of Texas Southwestern Medical Center · Dallas, TX
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.