Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care
Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care: CRT
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years to 24 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
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
Study sites (3)
PA
- University of Pittsburgh · Pittsburgh, PA 15261Phillip Schnarrs, PhD · Study contactMore trials in Pittsburgh
TX
- Steve Hicks School of Social Work at the University of Texas at Austin · Austin, TX 78705Lauren Gulbas, PhD · Study contactMore trials in Austin
- University of Texas Southwestern Medical Center · Dallas, TX 75390Emily Levy-Kamugisha, MD · Study contactMore trials in Dallas