- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01652430
Experiential Avoidance in Combat Veterans With and Without Posttraumatic Stress Disorder
January 6, 2015 updated by: VA Eastern Colorado Health Care System
This study plans to examine if symptoms of PTSD affect how Veterans who have served in combat think and react to certain information, and whether or not this has an influence on suicidal thoughts.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
78
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
-
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Colorado
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Denver, Colorado, United States, 80220
- Denver VA Medical Center
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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 to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The sample for the current project will be recruited from the group of veterans receiving or eligible to receive outpatient mental health services at the Denver VA Medical Center who have served in combat who may or may not have a diagnosis of PTSD.
Description
Inclusion Criteria:
- History of combat service
- Diagnosis of PTSD confirmed by the CAPS or
- No current diagnosis of PTSD
- Age 18-65
Exclusion Criteria:
- Inability to adequately respond to questions regarding the informed consent procedure.
- History of significant neurological disease
- Diagnosis of Schizophrenia or other Psychosis
- Alcohol abuse/dependence or illicit drug use in the two weeks prior to testing
- No history of combat service
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
Cohorts and Interventions
Group / Cohort |
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PTSD cohort
|
No PTSD cohort
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Beck Scale for Suicidal ideation
Time Frame: One time
|
One time
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nazanin Bahraini, Ph.D., VA Eastern Colorado Healthcare System/MIRECC
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
October 1, 2010
Primary Completion (Actual)
July 1, 2013
Study Completion (Actual)
July 1, 2013
Study Registration Dates
First Submitted
December 9, 2011
First Submitted That Met QC Criteria
July 25, 2012
First Posted (Estimate)
July 30, 2012
Study Record Updates
Last Update Posted (Estimate)
January 8, 2015
Last Update Submitted That Met QC Criteria
January 6, 2015
Last Verified
July 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10-0159
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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