Status:
COMPLETED
Innovative Service Delivery for Secondary Prevention of PTSD
Lead Sponsor:
Charleston Research Institute
Collaborating Sponsors:
United States Department of Defense
Conditions:
PTSD
Eligibility:
All Genders
21+ years
Phase:
NA
Brief Summary
The purpose of this study is to determine whether therapy for Operation Iraqi Freedom/Operation Enduring Freedom (OIF/OEF) veterans with Post-traumatic Stress Disorder (PTSD) symptoms can be delivered...
Detailed Description
OIF and OEF service men and women exposed to high levels of violence are at risk for developing mental health disorders including Post-traumatic Stress Disorder (PTSD) and Major Depressive Disorder (M...
Eligibility Criteria
Inclusion
- Participants will be OIF/OEF military personnel,
- age 21 and above, and
- with symptoms of posttraumatic stress disorder (PTSD) assigned on the basis of the Clinician Administered PTSD Scale (CAPS) and PTSD Checklist-Military (PCL-M).
Exclusion
- Actively psychotic or demented persons,
- individuals with both suicidal ideation and clear intent, and
- individuals meeting criteria for substance dependence will be excluded from participation.
Key Trial Info
Start Date :
March 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2015
Estimated Enrollment :
280 Patients enrolled
Trial Details
Trial ID
NCT01177488
Start Date
March 1 2008
End Date
February 1 2015
Last Update
September 14 2015
Active Locations (2)
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1
Medical University of South Carolina
Charleston, South Carolina, United States, 29403
2
Ralph H. Johnson VAMC
Charleston, South Carolina, United States, 29403