Status:
RECRUITING
Chronic Pain Management In Primary Care Using Behavioral Health Consultants
Lead Sponsor:
The University of Texas Health Science Center at San Antonio
Collaborating Sponsors:
Uniformed Services University of the Health Sciences
Massachusetts General Hospital
Conditions:
Chronic Pain
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this randomized pragmatic trial is to assess the effect of monthly booster contacts on long-term Brief Cognitive Behavioral Therapy for Chronic Pain (BCBT-CP) pain outcomes compared to ...
Detailed Description
The proposed study is the first effort to test a manualized cognitive-behavioral therapy intervention for chronic pain delivered by behavioral health providers working in primary care clinics. If succ...
Eligibility Criteria
Inclusion
- DoD/MHS beneficiary (including active duty service members, veterans, and family members) age 18 and older.
- Presenting with a chronic pain complaint (pain occurring more days than not over the past three months that is ongoing at the time of baseline evaluation).
- Referred for BCBT-CP with a BHC by a Primary Care provider.
- Speaks and reads/understands English well enough to fully participate in the intervention and to reliably complete assessment measures.
Exclusion
- Scheduled for a planned pain-related surgery or pain intervention within 6 weeks of enrollment (because the intervention may obscure BCBT-CP outcomes).
- Inability or unwillingness of individual to give written informed consent.
- Experiencing another health problem of higher priority for care or that prohibits ability to attend BCBT-CP or research appointments.
- Some research activities (i.e., Focus Groups) will include Clinic Providers and Staff:
- Inclusion Criteria for Clinic Provider/Staff Participants
- BHC trained to deliver care according to the Chronic Pain Clinical Pathway
- Clinic providers/staff caring for patient participants enrolled in this study
- Exclusion Criteria for Clinic Provider/Staff Participants: none
Key Trial Info
Start Date :
August 17 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 1 2027
Estimated Enrollment :
716 Patients enrolled
Trial Details
Trial ID
NCT04680000
Start Date
August 17 2021
End Date
January 1 2027
Last Update
May 13 2025
Active Locations (5)
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1
Uniformed Services University for the Health Sciences
Bethesda, Maryland, United States, 20814
2
Fort Cavazos
Fort Hood, Texas, United States, 76544
3
University of Texas Health Science Center San Antonio
San Antonio, Texas, United States, 78229
4
Wilford Hall Ambulatory Surgical Center
San Antonio, Texas, United States, 78236-9908