PTSD Clinical Trial
Official title:
Effects of Mindfulness-Based Cognitive-Behavioral Conjoint Therapy on PTSD and Relationship Function
Verified date | October 2018 |
Source | VA Office of Research and Development |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to first adapt Cognitive Behavioral Conjoint Therapy for PTSD for Operation Enduring Freedom and Operation Iraqi Freedom (OEF-OIF) Veterans diagnosed with PTSD and their intimate partners by (1) reducing the overall length of treatment from 15 weeks to 10 weeks through the use of a weekend couple retreat to deliver the first two of three phases of the three-phase protocol; and (2) by integrating mindfulness interventions as a way to mitigate the short, more condensed treatment. Secondly, this study will examine the effects of this adapted Mindfulness-Based Cognitive-Behavioral Conjoint Therapy on PTSD symptoms and intimate relationship functioning.
Status | Completed |
Enrollment | 92 |
Est. completion date | December 31, 2014 |
Est. primary completion date | June 30, 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Veteran must: - be enrolled in outpatient treatment - have a confirmed diagnosis of PTSD - have no major change in psychiatric medication for at least 1 month - have a partner mutually committed to maintaining the relationship for the duration of the intervention - willing to forgo initiating psychotherapy for PTSD or other conditions during the study Exclusion Criteria: - severe physical or sexual relationship aggression in the past year - current suicidal/homicidal intent (Veteran or partner) - cognitive impairment that precludes understanding session content (either Veteran or partner) - current substance dependence of Veteran or partner - uncontrolled psychotic or bipolar disorder in Veteran or partner - PTSD diagnosis in the partner - self-mutilation or self-injury within the previous 6 months by Veteran or partner - unwilling to have therapy or CAPS sessions video or audio recorded |
Country | Name | City | State |
---|---|---|---|
United States | Richard L. Roudebush VA Medical Center, Indianapolis, IN | Indianapolis | Indiana |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinician-Administered PTSD Scale (CAPS) | The Clinician Administered PTSD Scale (CAPS; Blake et al., 1995) is a semi-structured interview that evaluates PTSD symptoms and diagnostic status according to the Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (APA, 2000). The intensity and frequency of each symptom is separately on a 5 point Likert scale ranging from zero to four. The total CAPS symptom severity score ranges from 0-136, with higher scores indicating greater PTSD symptoms severity. For the purposes of this study, a score of 45 or greater confirmed a diagnosis of PTSD. | treatment end (approximately 10 weeks after session 1 of the interventions) |
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