Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care
Recruiting · NCT05869552 · Interventional (participants receive a specific treatment) · Lead sponsor: Elizabeth Arnold
View the official record on ClinicalTrials.gov →Interventions studied
STAT-PCYST-III
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.
Who can take part
Age range
18 Years to 24 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- be aged 18-24 at the time of enrollment
- not have received mental health services in the past 90 days, excluding medication and case management
- English-speaking
- screen positive for suicide risk
Exclusion criteria
- are actively suicidal
- have a developmental disability that would preclude them from participating in the study intervention
- who are impaired due to psychosis, mania, or substance use that would prevent them from providing consent.
- Participants will also be excluded at YST-III sites if they are unable to identify a minimum of one support person to participate in the intervention with them
Where it is running
3 locations listed across 2 US states.
- University of Pittsburgh - Pittsburgh, Pennsylvania, United States
- Steve Hicks School of Social Work at the University of Texas at Austin - Austin, Texas, United States
- University of Texas Southwestern Medical Center - Dallas, Texas, United States