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Optimizing Chronic Pain Care With Mindfulness and Chronic Pain Management Visits

StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗

Record History

  1. Phase: Not applicable to Phase 3 Site details revised at 3 of 3 sitesv6 Show 1 more changeShow less
    • Site details revised at 3 of 3 sites
  2. Site contacts updated at 2 of 3 sites Eligibility criteria expanded, about 1 wordv5 Show 1 more changeShow less
    • Eligibility criteria expanded, about 1 word

    See this version in full on ClinicalTrials.gov ↗

  3. Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Nov 1, 2024 to Feb 25, 2025 · Study sites: 2 to 3v4 Show 2 more changesShow less
    • Start date changed from estimate of Nov 1, 2024 to Feb 25, 2025
    • Study sites: 2 to 3
  4. Primary and study completion dates: May 1, 2030 to May 1, 2028 Start date: May 6, 2024 to Nov 1, 2024v3 Show 1 more changeShow less
    • Start date: May 6, 2024 to Nov 1, 2024
  5. Re-verified, no change to tracked fieldsv2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 primary aim of this implementation-effectiveness trial is to examine the effectiveness of Mindfulness-Oriented Recovery Enhancement (MORE) and patient-centered chronic pain management visits in primary care as interventions to reduce chronic pain, improve quality of life, and reduce opioid-related harms among chronic pain patients on long-term opioid therapy.
Trial Details
NCT Number NCT06387290
Lead Sponsor University of Utah
Collaborators: Rutgers University
Conditions Chronic Pain, Prescription Opioid Misuse, Substance-Related Disorders, Pain, Narcotic-Related Disorders, Chemically-Induced Disorders, Mental Disorders, Opioid-Related Disorders +1 more
Enrollment 300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov