- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01627548
UCLA Couples Counseling for Combat Veterans (CCCV)
October 31, 2022 updated by: Shirley Glynn, University of California, Los Angeles
UCLA Welcome Back Veterans Family Resilience Center Couples Counseling for Combat Veterans
A pilot intervention of an existing intervention adapted for the returning warfighter population: a couples treatment for PTSD, Structured Approach Therapy (SAT), which emphasizes reducing the PTSD avoidance/numbing symptoms that are corrosive in families.
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
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Los Angeles, California, United States, 90095
- UCLA Semel Institute
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- OIF/OEF/ OND veteran with at least one deployment
- In a cohabitating relationship for 6 months or longer
- Cohabitating 50% of the time or more
- Diagnosed with PTSD or meets the diagnosis criteria for PTSD as related to deployment experience (CAPS)
- Ability to make weekly appointments
- Willingness to commit to change
Exclusion Criteria:
- Receiving an evidence-based treatment for PTSD within the past 6 months
- Receiving couples therapy within the last 6 months
- Moderate or excessive physical violence within the past 3 months (CTS)
- Alcohol/substance dependence (SCID)
- Known domestic violence/abuse (CTS)
- Symptoms of psychosis within the past 3 months
- Unstable psychiatric medicine usage or on regimen less than 3 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: Waitlisted Intervention
Couple will be consented, assessed and randomized to a waitlist of 4 months.
The couple will be reassessed at 8 weeks and prior to initiating intervention.
|
The SAT treatment is provided in 12 weekly 50-minute sessions and is fully manualized.
First, couple-based exposure techniques are used to address anxiety about intimacy, increasing the traumatized person's ability to engage in social and relational behaviors that promote bonding and satisfaction.
Second, as anxiety decreases, couple-based techniques are also used to increase the positive experiences the couple is having.
These activities expose the traumatized person to positive feelings instead of anxiety, so that he/she may become desensitized to the anxiety caused by the closeness, and more comfortable engaging in intimate behaviors.
|
|
ACTIVE_COMPARATOR: Immediate Intervention
Eligible couples who are randomized to immediate intervention will begin sessions with a trained interventionist within weeks of consent and initial assessments
|
The SAT treatment is provided in 12 weekly 50-minute sessions and is fully manualized.
First, couple-based exposure techniques are used to address anxiety about intimacy, increasing the traumatized person's ability to engage in social and relational behaviors that promote bonding and satisfaction.
Second, as anxiety decreases, couple-based techniques are also used to increase the positive experiences the couple is having.
These activities expose the traumatized person to positive feelings instead of anxiety, so that he/she may become desensitized to the anxiety caused by the closeness, and more comfortable engaging in intimate behaviors.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Improved couples communication as measured by standardized assessments
Time Frame: 4-6 months
|
4-6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Shrley M Glynn, PhD, University of California, Los Angeles
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2012
Primary Completion (ANTICIPATED)
November 1, 2013
Study Completion (ANTICIPATED)
November 1, 2013
Study Registration Dates
First Submitted
June 21, 2012
First Submitted That Met QC Criteria
June 21, 2012
First Posted (ESTIMATE)
June 25, 2012
Study Record Updates
Last Update Posted (ACTUAL)
November 3, 2022
Last Update Submitted That Met QC Criteria
October 31, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 11-003109
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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