Posttraumatic Stress Disorder Clinical Trial
Official title:
Group vs. Individual Cognitive Processing Therapy for Combat-related PTSD
Verified date | March 2017 |
Source | VA Boston Healthcare System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to conduct a randomized controlled trial to compare group and individual CPT-C for the treatment of PTSD in OIF/OEF military personnel.
Status | Completed |
Enrollment | 300 |
Est. completion date | January 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adult male and female active duty, activated Reservist, or activated National Guard OIF/OEF military personnel or OIF/OEF veterans seeking treatment for PTSD - Diagnosis of PTSD determined by a clinician-administered Posttraumatic Stress Scale (PSSI) - Person has experienced a Criterion A event that is a specific combat-related event or high magnitude operational experience that occurred during a military deployment in support of OIF/OEF. The diagnosis of PTSD may be indexed to that event or to another Criterion A event. - Be over the age of 18 - Speak and read English - Be stable on any psychotropic medications they may be taking. Exclusion Criteria: - Current suicide or homicide risk meriting crisis intervention - Active psychosis - Moderate to severe brain damage (as determined by the inability to comprehend the baseline screening questionnaires) |
Country | Name | City | State |
---|---|---|---|
United States | Fort Hood Army Base | Fort Hood | Texas |
Lead Sponsor | Collaborator |
---|---|
Duke University | STRONG STAR Consortium, The University of Texas Health Science Center at San Antonio, VA Boston Healthcare System |
United States,
Resick PA, Wachen JS, Dondanville KA, Pruiksma KE, Yarvis JS, Peterson AL, Mintz J; and the STRONG STAR Consortium., Borah EV, Brundige A, Hembree EA, Litz BT, Roache JD, Young-McCaughan S. Effect of Group vs Individual Cognitive Processing Therapy in Act — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in PTSD symptoms as measured by thePosttraumatic Stress Disorder Checklist-Stressor-specific Version (PCL-S) | PCL-S measures symptoms of posttraumatic stress disorder in response to a specific stressor. | Baseline, weekly during treatment, posttreatment, 6-month and 12-month follow-up | |
Secondary | Change from baseline in depressive symptoms as measured by the Beck Depression Inventory-II | The BDI-II is one of the most widely used instruments for measuring the severity of depressive symptoms. It consists of 21 items that assess both affective and somatic symptoms related to depression and depressive disorders. Each item is composed of four statements that reflect symptom severity. The statements are scaled from 0 (no disturbance) to 3 (maximal disturbance). Scores on all items are summed to obtain a total severity score. | Baseline, weekly during treatment, posttreatment, 6-month, and 12-month follow-up |
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