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Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care
NCT05869552 · View on ClinicalTrials.gov ↗
Study 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.
Conditions Studied
Interventions
- OTHER STAT-PC
- OTHER YST-III
Study Locations (3)
Texas
- Steve Hicks School of Social Work at the University of Texas at Austin — Austin
- University of Texas Southwestern Medical Center — Dallas
Pennsylvania
- University of Pittsburgh — Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,485 participants |
| Start Date | 2023-07-13 |
| Est. Completion | 2027-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05869552
The ClinicalTrials.gov registry entry for NCT05869552 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,485 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Elizabeth Arnold, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Suicide appearing as the primary indexed condition, and to 2 interventions — of which STAT-PC is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05869552 reports 3 study locations spanning 2 distinct geographic areas — top geographies include Texas, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05869552 about?
NCT05869552 is a clinical study titled "Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care". 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 re...
What is the current status of trial NCT05869552?
This trial is currently recruiting. It is a NA study. The enrollment target is 1,485 participants. The study started on 2023-07-13. Estimated completion is 2027-03.
What conditions does trial NCT05869552 study?
This clinical trial studies the following conditions: Suicide, Suicidal Ideation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05869552?
The interventions under investigation include: STAT-PC (OTHER), YST-III (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05869552?
This trial is sponsored by Elizabeth Arnold, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05869552 being conducted?
This trial has 3 study locations across Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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