Actively Recruiting

Phase 2
Age: 13Years - 24Years
All Genders
NCT05304065

Safe Treatment for Emergency Presentation for Suicidal Ideation and Behavior in Youth

Led by University of California, Los Angeles · Updated on 2025-12-31

1600

Participants Needed

5

Research Sites

219 weeks

Total Duration

On this page

Sponsors

U

University of California, Los Angeles

Lead Sponsor

D

Duke University

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Safe Treatment for Emergency Presentation for Suicidal Ideation and Behavior in Youth

Who Can Participate

Age: 13Years - 24Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 13 and 24 years
  • Suicidal behavior or thoughts with plan or intent in the past week
Not Eligible

You will not qualify if you...

  • Symptoms or illness preventing informed consent or participation (e.g., active psychosis, drug dependence)
  • Lack of locator information
  • Youth not fluent in English
  • Parent not fluent in English or Spanish

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Ronald Reagan Medical Center

Los Angeles, California, United States, 90095-6968

Actively Recruiting

2

Olive View UCLA Education and Research Center

Sylmar, California, United States, 91342

Actively Recruiting

3

Duke University

Durham, North Carolina, United States, 27708

Actively Recruiting

4

Brown University

Providence, Rhode Island, United States, 02912

Actively Recruiting

5

University of Utah

Salt Lake City, Utah, United States, 84112

Actively Recruiting

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Research Team

L

Lucas Zullo, PhD

CONTACT

J

Jocelyn I Meza, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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