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2 for Post-Traumatic Stress Disorder

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
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights


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).


Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Using an intent to treat analysis, subjects' maintained employed rate is measured using the Employment Index.
Secondary outcome measures
Using an intent-to-treat analysis, the change from baseline to endpoint in PTSD symptoms is compared between groups using the Clinician Administered PTSD Scale (CAPS).

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)
First Studied
Drug Approval Stage
How many patients have taken this drug
Supported Employment (SE)

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
875 Previous Clinical Trials
329,886 Total Patients Enrolled
Lori L. Davis, M.D.Principal InvestigatorTuscaloosa Veterans Affairs Medical Center
~6 spots leftby Jul 2025