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Safe Treatment for Emergency Presentation for Suicidal Ideation and Behavior in Youth
NCT05304065 · View on ClinicalTrials.gov ↗
Study Summary
This randomized comparative effectiveness trial will compare two evidence-based approaches to emergency care for youth ages 13-24 who present to the Emergency Department (ED) with suicidal ideation or behavior. Outcomes will be monitored at baseline and at 3, 6 \& 12 month follow-up assessments.
Interventions
- BEHAVIORAL SAFETY-A within usual ED Care
- BEHAVIORAL Combined SAFETY-A within usual ED Care + CLASP Therapeutic Follow-Up Contacts
Study Locations (5)
California
- Ronald Reagan Medical Center — Los Angeles
- Olive View UCLA Education and Research Center — Sylmar
North Carolina
- Duke University — Durham
Rhode Island
- Brown University — Providence
Utah
- University of Utah — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,600 participants |
| Start Date | 2022-10-17 |
| Est. Completion | 2026-12-31 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05304065
The ClinicalTrials.gov registry entry for NCT05304065 describes a study currently listed as recruiting. It is categorized as Phase 2, 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 1,600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Los Angeles, which has 829 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Suicide appearing as the primary indexed condition, and to 2 interventions — of which SAFETY-A within usual ED Care 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: NCT05304065 reports 5 study locations spanning 4 distinct geographic areas — top geographies include California, North Carolina, Rhode Island. 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 NCT05304065 about?
NCT05304065 is a clinical study titled "Safe Treatment for Emergency Presentation for Suicidal Ideation and Behavior in Youth". This randomized comparative effectiveness trial will compare two evidence-based approaches to emergency care for youth ages 13-24 who present to the Emergency Department (ED) with suicidal ideation or behavior. Outcomes will be monitored at baseline and at 3, 6 \& 12 month follow-up assessments.
What is the current status of trial NCT05304065?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 1,600 participants. The study started on 2022-10-17. Estimated completion is 2026-12-31.
What conditions does trial NCT05304065 study?
This clinical trial studies the following conditions: Suicide, Suicidal, Self-Harm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05304065?
The interventions under investigation include: SAFETY-A within usual ED Care (BEHAVIORAL), Combined SAFETY-A within usual ED Care + CLASP Therapeutic Follow-Up Contacts (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05304065?
This trial is sponsored by University of California, Los Angeles, which has 829 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05304065 being conducted?
This trial has 5 study locations across California, North Carolina, Rhode Island, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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