Actively Recruiting
Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care
Led by Elizabeth Arnold · Updated on 2025-11-06
1485
Participants Needed
3
Research Sites
189 weeks
Total Duration
On this page
Sponsors
E
Elizabeth Arnold
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be aged 18 to 24 years at the time of enrollment
- Have not received mental health services in the past 90 days, except for medication and case management
- Be able to speak English
- Screen positive for suicide risk
You will not qualify if you...
- Be actively suicidal
- Have a developmental disability that prevents participation in the study intervention
- Have impairments due to psychosis, mania, or substance use that prevent giving consent
- At YST-III sites, be unable to identify at least one supportive adult willing to participate with you
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
University of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15261
Actively Recruiting
2
Steve Hicks School of Social Work at the University of Texas at Austin
Austin, Texas, United States, 78705
Actively Recruiting
3
University of Texas Southwestern Medical Center
Dallas, Texas, United States, 75390
Actively Recruiting
Research Team
E
Elizabeth Arnold, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here