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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

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 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

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

Find a Location

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
891 Previous Clinical Trials
332,378 Total Patients Enrolled
Lori L. Davis, M.D.Principal InvestigatorTuscaloosa Veterans Affairs Medical Center
~6 spots leftby Sep 2025
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