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Chronic Pain Management In Primary Care Using Behavioral Health Consultants

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date changed from estimate of Jun 30, 2026 to Sep 11, 2026 Show 4 more changesShow less
    • Study sites: 5 to 3
    • Eligibility criteria expanded, about 9 words
    • Secondary endpoints: details revised at 5 of 6 entries
    • Collaborators: 6 to 7
  2. Primary completion pushed from May 2026 to Jun 30, 2026v10
  3. Trial status: Recruiting to Active, Not Recruiting
    • Site details revised at 5 of 5 sites
    v9
  4. Study sites revised (5)v8
  5. Primary completion date: Jun 2025 to May 2026
    • Study completion date: Jun 2026 to Jan 2027
    • Study description expanded, about 101 words
    v7
Show 5 earlier versionsHide 5 earlier versions
  1. Primary completion date: Jun 2024 to Jun 2025
    • Study completion date: Jun 2025 to Jun 2026
    v6
  2. Primary completion date: Feb 2024 to Jun 2024
    • Study completion date: Feb 2025 to Jun 2025
    v5
  3. Study sites: 2 to 5v4
  4. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jul 2021 to Aug 17, 2021
    • Site details revised at 2 of 2 sites
    v3
  5. Start date: Feb 2021 to Jul 2021v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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 BCBT-CP without a booster in 716 Military Health Systems (MHS) beneficiaries referred to a Behavioral Health Consultant (BHC) for pain management using BCBT-CP. Patients will be randomly assigned to receive either standard BCBT-CP (working with a BHC in the medical home clinic) or standard BCBT-CP with adjunctive monthly booster contacts. Patient participants will be assessed 3-, 6-, 12- and 18-Months following their first appointment for BCBT-CP. Prospective data will be supplemented by a national data pull in collaboration with the Defense Health Agency and the Uniformed Services University Center for Rehabilitation Sciences Research. Pulled data will include a national deidentified dataset of electronic health record data for all individuals treated in the military health system who had access to a Behavioral Health Consultant for the treatment under study in this trial.
Trial Details
NCT Number NCT04680000
Lead Sponsor The University of Texas Health Science Center at San Antonio
Collaborators: Uniformed Services University of the Health Sciences, Massachusetts General Hospital, Defense Health Agency, 59th Medical Wing, Brooke Army Medical Center, C.R.Darnall Army Medical Center, United States Department of Defense
Conditions
(from sponsor)		 Chronic Pain
Related terms Chronic Pain
Enrollment 716 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov