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A Comparison of Cognitive Processing Therapy (CPT) Versus Present Centered Therapy (PCT) for Veterans

Not Applicable
Completed
Conditions
PTSD
Interventions
Behavioral: Present Centered Therapy
Behavioral: Cognitive Processing Therapy
Registration Number
NCT00607815
Lead Sponsor
VA Office of Research and Development
Brief Summary

The purpose of this study is to compare the effectiveness of Cognitive Processing Therapy (CPT) versus Present Centered Therapy (PCT) for male OEF/OIF Veterans with combat related PTSD.

Detailed Description

The purpose of this study is to compare the effectiveness of Cognitive Processing Therapy (CPT) versus Present Centered Therapy (PCT) for male OEF/OIF Veterans with combat related PTSD.

CPT has been shown to be effective in treating trauma survivors in several treatment outcome studies, but utility with Veterans has only been examined with male Veterans in one small pilot study. In addition CPT has never been compared to a treatment as usual or supportive psychotherapy condition to control for the specific and nonspecific elements of treatment. Although Cognitive Processing Therapy is one of the main treatment modalities at several VA's, including Cincinnati, it has never been compared to PCT, nor has it been used in a large, randomized study of male OEF/OIF Veterans. It is hypothesized that individual receiving CPT will show a larger reduction in posttraumatic stress disorder and related symptoms than those individuals receiving PCT.

All male OEF/OIF Veterans will be screened for their appropriateness for the study by phone screen and then by an assessment technician. The Veteran will be assessed at pre, post, 3-month, and 1-year follow-up. The assessment technicians will be blind to the participant's condition. CPT is a 12 week long individual psychotherapy treatment shown to be effective at reducing PTSD and related symptoms for survivors of various types of traumas, including combat. PCT is a supportive counseling treatment that has been utilized as an alternative to waitlist control in VA cooperative studies of PTSD.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
79
Inclusion Criteria
  • PTSD;
  • memory of the trauma;
  • able to read/write;
  • must be stable on medication for 3 months
Exclusion Criteria
  • Psychosis;
  • suicidal/homicidal intent;
  • alcohol/substance dependence;
  • no memory of the trauma

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Present Centered TherapyPresent Centered TherapyPresent Centered Therapy
Cognitive Processing TherapyCognitive Processing TherapyCognitive Processing Therapy
Primary Outcome Measures
NameTimeMethod
Clinician Administered PTSD ScalePost-treatment, at 3 months and 1 year

Clinician-rated PTSD symptom severity; higher is worse; range at post-treatment is 0 to 80; scale scores are summed.

PTSD Checklist (PCL)post-treatment, at 3 months and 1 year

17-item patient self-reported PTSD severity; higher is worse; range at post-treatment is 17-73; scale scores are summed

Secondary Outcome Measures
NameTimeMethod
Beck Depression Inventory - II (BDI-II)post-treatment, at 3 months and 1 year

Gold-standard, self-reported depression severity measure; higher is worse; post-treatment range is 2-45. scale scores are summed.

State-Trait Anger Scale (STAXI)post-treatment, at 3 months and 1 year

Self-reported trait anger; subscale score is summed; higher is worse; range at post-treatment is 10-37.

State-Trait Anxiety Scalepost-treatment, at 3 months and 1 year

Self-reported state anxiety; higher is worse; scale score is summed; range at post-treatment is 20-73.

Trial Locations

Locations (1)

Cincinnati VA Medical Center, Cincinnati, OH

🇺🇸

Cincinnati, Ohio, United States

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