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2 for Post-Traumatic Stress Disorder
N/A
Waitlist Available
Led By Lori L. Davis, M.D.
Research Sponsored by Tuscaloosa Research & Education Advancement Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This prospective randomized study evaluates the impact of Supportive Employment (SE) compared to standard vocational rehabilitation (VRP) on occupational, sobriety, psychiatric, and quality of life outcomes and health care costs for veterans with chronic posttraumatic stress disorder (PTSD).
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: 2Experimental Treatment1 Intervention
Supported Employment (SE)
Group II: 1Active Control1 Intervention
Standard Vocational Rehabilitation (VRP)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Supported Employment (SE)
2017
N/A
~70
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Who is running the clinical trial?
Tuscaloosa Research & Education Advancement CorporationLead Sponsor
14 Previous Clinical Trials
2,247 Total Patients Enrolled
United States Department of DefenseFED
904 Previous Clinical Trials
333,129 Total Patients Enrolled
Lori L. Davis, M.D.Principal InvestigatorTuscaloosa Veterans Affairs Medical Center
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