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Critical Time Intervention for Homelessness
Phase 1
Waitlist Available
Led By Sonya Emi Gabrielian, MD MPH
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, 4 years
Awards & highlights
Study Summary
This trial will help determine if an evidence-based practice called Critical Time Intervention can help improve housing outcomes for homeless Veterans.
Who is the study for?
This trial is for Veterans who have experienced homelessness and are part of the Grant and Per Diem (GPD) case management aftercare program in 7 Veterans Integrated Service Networks. It's designed to help them as they transition into housing by providing six months of specialized case management.Check my eligibility
What is being tested?
The study is testing Critical Time Intervention (CTI), a time-limited support strategy, along with External Facilitation and Replicating Effective Programs, to improve the housing stability of homeless-experienced Veterans in the GPD program.See study design
What are the potential side effects?
Since this trial involves social support interventions rather than medical treatments, traditional physical side effects are not applicable. However, participants may experience stress or emotional discomfort during their transition.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, 4 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, 4 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Dollars spent delivering CTI at each site
Fidelity to CTI
Sustainment of CTI
Secondary outcome measures
Cost of CTI as Implemented
Cost of Implementation Strategies
Hospitalization rates
+3 moreTrial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Replicating Effective Programs (REP)Experimental Treatment2 Interventions
A stakeholder-informed training and technical assistance implementation strategy
Group II: REP + External Facilitation (Enhanced REP)Active Control3 Interventions
REP plus site specific weekly facilitation to support CTI implementation.
Group III: Control GroupActive Control1 Intervention
No CTI implementation
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Critical Time Intervention
2016
N/A
~240
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,621 Previous Clinical Trials
3,323,348 Total Patients Enrolled
8 Trials studying Homelessness
1,080 Patients Enrolled for Homelessness
University of California, Los AngelesOTHER
1,538 Previous Clinical Trials
10,266,878 Total Patients Enrolled
Center for the Advancement of Critical Time InterventionUNKNOWN
1 Previous Clinical Trials
15,195 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- N/A
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