๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-11-04

Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care (NCT05869552)

Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care: CRT

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: Elizabeth Arnold

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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 join: Review the eligibility criteria below.

Location: University of Pittsburgh โ€” Pittsburgh, Pennsylvania

Age range: 18 Years to 24 Years

๐Ÿงช Interventions in This Study

  • STAT-PC (OTHER)
  • YST-III (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (3 Sites)

  • University of Pittsburgh โ€” Pittsburgh, Pennsylvania
  • Steve Hicks School of Social Work at the University of Texas at Austin โ€” Austin, Texas
  • University of Texas Southwestern Medical Center โ€” Dallas, Texas

๐Ÿ“ž Contact the Study Coordinator

Phone: (859) 562-3751

Email: Liz.Arnold@uky.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Suicide clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—