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N/A N=85 Randomized Treatment

The Impact of Vocational Rehabilitation on Mentally III Veterans

Posttraumatic Stress Disorder (PTSD)

Enrolled (actual)
85
Serious AEs
18.8%
Results posted
Mar 2015
Primary outcome: Primary: Obtain Competitive Employment — 12; 32 participants — p=<0.001

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Vocational Rehabilitation Program (VRP) (Behavioral); Individual Placement and Support (IPS) (Behavioral)
Age
Adult · 19+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Apr 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Obtain Competitive Employment
12; 32 <0.001 sig
SECONDARY
PTSD, Depression, Disability Outcomes
78.4; 77.3; 12.2; 12.3; 5.0; 4.8 >0.05
SECONDARY
Employment Outcomes (Weeks Competitively Employed)
6.8; 21.6 <0.001 sig
SECONDARY
Employment Outcomes (Days Competitively Employed
29.3; 83.8
SECONDARY
Employment Outcomes (Hours Competitively Employed)
236; 656
SECONDARY
Employment Outcomes (Gross Income Competitive)
2,601; 9,264
SECONDARY
Employment Outcomes (Total Gross Income From All Sources
3,909; 13,449

Summary

To study the impact of Individual Placement and Support (IPS) supported employment (SE) compared to treatment-as-usual vocational rehabilitation program (VRP) for veterans with posttraumatic stress disorder (PTSD).

Eligibility Criteria

Inclusion Criteria

  • Male or Female
  • Age, greater than or equal to 19 and less than 61.
  • Enrollment in the TVAMC VRP
  • Signed informed consent
  • Chronic post-traumatic stress disorder
  • Any race or ethnic origin
  • Anticipation of remaining in the catchment area for the 12-month study duration

Exclusion Criteria

  • Lifetime history of severe traumatic brain injury that has resulted in severe cognitive impairment
  • History of schizophrenia, schizoaffective, disorder, or bipolar I disorder
  • Pending litigation
  • In need of immediate detoxification.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00333801). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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