Group-Based Mindfulness for Patients with Chronic Low Back Pain in the Primary Care

Information

  • Research Project
  • 10265606
  • ApplicationId
    10265606
  • Core Project Number
    UH3AT010621
  • Full Project Number
    5UH3AT010621-03
  • Serial Number
    010621
  • FOA Number
    RFA-AT-19-004
  • Sub Project Id
  • Project Start Date
    9/28/2019 - 5 years ago
  • Project End Date
    8/31/2024 - 3 months ago
  • Program Officer Name
    WEBER, WENDY J
  • Budget Start Date
    9/1/2021 - 3 years ago
  • Budget End Date
    8/31/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    03
  • Suffix
  • Award Notice Date
    9/2/2021 - 3 years ago

Group-Based Mindfulness for Patients with Chronic Low Back Pain in the Primary Care

Chronic low back pain (cLBP) is one of the most common conditions treated in the primary care setting, yet treatment remains unsatisfactory for many patients. The opioid crisis has underscored the urgency of alleviating patients' cLBP with effective therapies, including evidence-based nonpharmacologic approaches. Mindfulness is effective for the treatment of cLBP yet remains underutilized as it has not been regularly woven into the outpatient clinical setting. Mindfulness-based Stress Reduction (MBSR) is now recommended by the American College of Physicians for initial treatment of cLBP. The next necessary step is to do a pragmatic clinical trial (PCT) with the goal of informing decision makers how this program can work in a real-life clinical setting and its impact on outcomes. We propose a PCT of this program titled ?OPTIMUM? (Optimizing Pain Treatment In Medical settings Using Mindfulness). It will be conducted with three health care system (HCS) sites (Boston Medical Center, MA, UPMC, Pittsburgh, PA, and Piedmont Health Services, in partnership with the University of North Carolina, Chapel Hill). Our primary goal is to determine the impact of this intervention under usual care circumstances. The rationale for this project is to inform key decision-makers how nonpharmacologic treatment can be integrated into routine care and the impact of this program on key outcomes. The specific aims UG3 Phase are the following: Aim 1: To plan and test a mindfulness clinical pain program, OPTIMUM, in the 3-HCS sites prior to the full PCT during the first 12- months of the project. Clearly defined milestones will be reached with guidance from the Collaboratory Coordinating Center. The specific aims UH3 Phase are: Aim 2. To integrate and test an evidence-based mindfulness clinical pain program, OPTIMUM, for patients with cLBP in the primary care setting. Four- hundred-fifty persons with cLBP ? 18 years of age will be randomized to 1) OPTIMUM (n=225) + PCP Usual Care; or 2) PCP Usual Care (n=225). Primary Hypothesis: patients in OPTIMUM will have significantly reduced pain at completion of the program and 6- and 12-months later, as compared to PCP Usual Care. Hypothesis 2: patients in OPTIMUM will have significantly improved physical and psychological function at completion of the program and 6- and 12-months later, as compared to PCP Usual Care. Hypothesis 3: patients in OPTIMUM will be less likely to start and more likely to reduce or stop an opioid prescription for cLBP as compared to those in PCP Usual Care. Aim 3. To evaluate use of healthcare resources by patients as documented in the electronic health record. Hypothesis: patients in OPTIMUM will have fewer emergency department visits, fewer hospitalizations, fewer imaging (CT/MRI), and fewer procedures (injections, surgery) than PCP usual care. Aim 4. To evaluate PCP and practice site use of, satisfaction with, and integration of OPTIMUM. Delivering a group mindfulness pain program in primary care is innovative and we expect it will increase the quality of, and satisfaction with cLBP care.

IC Name
National Center for Complementary & Integrative Health
  • Activity
    UH3
  • Administering IC
    AT
  • Application Type
    5
  • Direct Cost Amount
    1349757
  • Indirect Cost Amount
    272319
  • Total Cost
    1622076
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    213
  • Ed Inst. Type
  • Funding ICs
    NINDS:1622076\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    NSS
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    BOSTON MEDICAL CENTER
  • Organization Department
  • Organization DUNS
    005492160
  • Organization City
    BOSTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021182908
  • Organization District
    UNITED STATES