Safe Treatment for Emergency Presentation for Suicidal Ideation and Behavior in Youth
NCT05304065 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 1600
Last updated 2025-12-31
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.
Conditions
- Self-Harm
- Suicide
- Suicidal
Interventions
- BEHAVIORAL
-
SAFETY-A within usual ED Care
SAFETY-A is a single session collaborative, strengths-based, developmentally nuanced, cognitive-behavioral intervention (CBT) to increase safety and mental health treatment initiation. The therapist works with the youth and family (or significant other, SO) separately and together to build hope and reasons for living, develop a personal safety plan, increase protective supports; and increase motivation for and linkage to treatment.
- BEHAVIORAL
-
Combined SAFETY-A within usual ED Care + CLASP Therapeutic Follow-Up Contacts
COMB, includes SAFETY-A within usual ED care plus CLASP therapeutic and caring follow-up contacts designed to strengthen safety and treatment initiation and engagement. Core functions of CLASP include: building hope/reducing hopelessness; enhancing social/family support; strengthening problem-solving; and increasing treatment initiation and engagement.
Sponsors & Collaborators
- collaborator OTHER
-
Brown University
collaborator OTHER - collaborator OTHER
-
Olive View-UCLA Education & Research Institute
collaborator OTHER -
RAND
collaborator OTHER -
Patient-Centered Outcomes Research Institute
collaborator OTHER -
University of California, Los Angeles
lead OTHER
Principal Investigators
-
Joan R Asarnow, PhD · University of California, Los Angeles
-
David Goldston, PhD · Duke University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 13 Years
- Max Age
- 24 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-10-17
- Primary Completion
- 2026-12-31
- Completion
- 2026-12-31
Countries
- United States
Study Locations
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