Actively Recruiting
Swift Outpatient Alternatives for Rapid Stabilization
Led by University of Washington · Updated on 2025-03-27
184
Participants Needed
1
Research Sites
216 weeks
Total Duration
On this page
Sponsors
U
University of Washington
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to improve the effective outpatient management of acute youth suicide risk by optimizing intervention components to build an efficient, evidence-based intervention that is responsive to the needs of, and coordinated with, providers in primary care settings. The main questions are: 1. What is the strongest combination of SOARS components associated with reduction in youth suicidal thoughts and behavior (STB)? 2. Do age and STB history moderate the impact of the effects of the SOARS intervention components? 3. Do therapeutic alliance, youth and caregiver self-efficacy account for changes in youth STBs? 4. What helps medical outpatient providers refer to SOARS and continue care after SOARS?
CONDITIONS
Official Title
Swift Outpatient Alternatives for Rapid Stabilization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Acute suicidal thoughts or a suicide attempt within the past month as indicated by positive responses to the Ask Suicide Screening Questionnaire (ASQ)
You will not qualify if you...
- Need for urgent medical care due to self-injury, psychosis, or eating disorder requiring inpatient care
- Intellectual disability requiring a different treatment approach
- Limited proficiency in English, Spanish, Vietnamese, or Chinese interfering with study assessments
- Unwillingness to participate in psychotherapy
- Caregiver unwilling or unable to participate
- Previous enrollment in SOARS program or related projects to avoid follow-up confusion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Seattle Children's
Seattle, Washington, United States, 98199
Actively Recruiting
Research Team
M
Molly Adrian
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
TREATMENT
Number of Arms
8
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