Telephone Cognitive Behavior Therapy for OEF Veterans With Pain
Completed · Not applicable
Conditions studied: Chronic Pain
In brief
We conducted a randomized clinical trial comparing telephone-delivered cognitive behavior therapy and pain education control. We enrolled 41 OEF/OIF/OND veterans with chronic pain and randomizing them into one of two treatment conditions. The study sample was recruited from primary care clinics at the San Francisco VA Medical Center and affiliated VA community-based outpatient clinics (CBOCs) in downtown San Francisco, Clearlake, Eureka, San Bruno, Santa Rosa, and Ukiah. Recruitment targeted OEF/OIF/OND veterans with pain disorders that involved muscle strain and inflammation, trauma to nerves, and/or central nervous system dysfunction. Both interventions were delivered by telephone and consisted of 12 sessions scheduled over a 20-week period. Pain management outcomes were measured at 10 weeks (mid-treatment), 20 weeks (post-treatment), 32 weeks (3-month follow-up), and 46 weeks (6-month follow-up). The sample size was chosen to provide greater than 80% power at a two-tailed alpha of 0.05. The study hypothesis, assessment methodology, and intervention procedures were based on the cognitive-behavioral model of chronic pain.
Key facts
- Study ID
- NCT01236196
- Run by
- US Department of Veterans Affairs
- People needed
- 41
- Starts
- 2010-10-01
- Expected to finish
- 2013-09-01
- Last updated by the study team
- 2014-12-23
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- To be eligible to participate in this study, potential subjects must have:
- access to a telephone
- documented pain for at least the past year
- a pain disorder involving muscle strain and inflammation, trauma to nerves, or central nervous system dysfunction
- pain condition must be stable
- must have no clear indication for specific medical/surgical intervention.
You may not qualify if…
- Patients were excluded who were:
- acutely psychotic
- cognitively impaired
- showed significant suicidal risk (history of multiple suicide attempts or actively suicidal)
- currently abusing alcohol or other drugs, including prescribed opioid pain medications
- patients were also excluded who had an unstable medical condition and clear indication for specific medical/surgical intervention in the near future.
Where it is running
- VA Medical Center, San Francisco — San Francisco, California, United States
Full record on ClinicalTrials.gov
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