Post-Traumatic Stress Disorder Clinical Trial
Official title:
Randomized Controlled Equivalence Trial Comparing Videoconference and Face-to-Face Delivery of Cognitive Processing Therapy for PTSD
The purpose of this study is to evaluate the equivalence of CPT treatment delivered remotely via telemental health (TMH) over videoconferencing or via traditional face-to face (FTF) treatment to veterans who have Post-traumatic Stress Disorder (PTSD) from a military-related stressor (i.e., combat, sexual assault, non-combat physical assault). The secondary objective is to determine if patients' ratings of PTSD symptoms, affect, social adjustment, therapy alliance, treatment satisfaction and therapist satisfaction, are equivalent between service-delivery conditions (TMH vs. FTF). A final objective is to develop web-based practice assignments to assist participants in the TMH condition with treatment adherence (completion of the between- session practice assignments).
Status | Completed |
Enrollment | 90 |
Est. completion date | November 2013 |
Est. primary completion date | November 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - 18 years of age or older - Literate in written English - Fluent in spoken English - Verified status as an OEF/OIF veteran - Current PTSD diagnosis - Index traumatic event related to military services - If taking psychotropic medication, remains stable Exclusion Criteria: - Under 18 years of age - Not literate in written English - Not fluent in spoke English - Current uncontrolled psychotic or bipolar disorder - Substance dependence - Current uncontrolled suicidal or homicidal ideation - Significant cognitive impairment that would interfere with completion of therapy tasks |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Edward J. Hines Jr. Veterans Hospital, Cares Research Foundation FWA00001322 | Hines | Illinois |
United States | Wm. S.Middleton Memorial Veterans Hospital | Madison | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
University of Wisconsin, Madison | VA Office of Research and Development |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Clinician Administered PTSD Scale(CAPS) score. | At baseline, post-treatment( after 6 weeks) and the 3-month follow-up period | No |
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