Skip to main content
Clinical Trials/NCT04770480
NCT04770480
Active, Not Recruiting
N/A

Exploring Non-pharmacological Approaches to Pain Management After Lumbar Surgery: A Randomized Controlled Trial

Dan Rhon3 sites in 1 country267 target enrollmentDecember 10, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Dan Rhon
Enrollment
267
Locations
3
Primary Endpoint
Pain, Enjoyment, and General Activity Scale (PEG-3)
Status
Active, Not Recruiting
Last Updated
10 months ago

Overview

Brief Summary

This study will compare the effectiveness of two pain management pathways (standard vs. enriched) for patients undergoing lumbar spine surgery in the Military Health System (MHS). Effectiveness will be based on post-surgery patient-centered outcomes and extent of opioid use. The study design is a 2-arm, parallel group, individual-randomized trial.

Detailed Description

The relevance of our model is supported by evidence that pain catastrophizing, self-efficacy and hypervigilance predict poor surgical outcomes and long-term opioid use. Surgery can exacerbate catastrophic thinking, especially if patients have unrealistic recovery expectations that go unmet. Physical therapy (PT) can improve chronic LBP (low back pain) outcomes, with effects mediated through changes in pain catastrophizing and self-efficacy. Mindfulness techniques help patients disentangle an experience (e.g., pain) from associated emotions and appraisals. Mindfulness can enhance emotion regulation and raise un-conscious behavioral responses (e.g., opioid use) to conscious consideration. The benefits of mindfulness for chronic pain are mediated by changes in hypervigilance and self-efficacy. Physical therapy and mindfulness can disrupt the self-reinforcing cycle of pain, catastrophic appraisal and unconscious behavioral response including opioid use. Our project examines an innovative strategy to integrate mindfulness and PT into an enriched surgical management pathway for individuals undergoing lumbar spine surgery. Patients at 3 different military hospitals will be randomized prior to surgery to two different treatment groups and followed for a period of 6 months, including the post-operative intervention phase.

Registry
clinicaltrials.gov
Start Date
December 10, 2021
End Date
March 30, 2026
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Dan Rhon
Responsible Party
Sponsor Investigator
Principal Investigator

Dan Rhon

Director, Primary Care Musculoskeletal Research Center

Brooke Army Medical Center

Eligibility Criteria

Inclusion Criteria

  • Tricare beneficiary receiving care in a participating MHS facility.
  • Age 18 - 75 years at the time of enrollment
  • Scheduled to undergo lumbar spine surgery within the next 60 days. Surgery may be laminectomy with or without fusions including lateral, transforaminal, posterior or anterior approach for 1-4 lumbar levels. Surgery may be performed in military or civilian facility
  • Indication for surgery may include disc herniation, degenerative disc disease, lumbar stenosis, degenerative spondylolisthesis or scoliosis.
  • Anticipates ability to attend treatment sessions over a 16 week period following the surgical procedure with no planned absence of 2 weeks or more for training, vacation or any purpose

Exclusion Criteria

  • Indication for surgery is infection, fracture, tumor, trauma or other indication requiring emergency surgery.
  • A microsurgical technique as the primary procedure, such as an isolated laminotomy or microdiscectomy
  • Surgical procedure is a revision or participant has undergone a lumbar surgical procedure in the past year.
  • Contra-indication to participation in post-operative exercise program including severe orthopedic injury limiting mobility, wheelchair dependency, neurological disorder impacting mobility, reliance on supplemental oxygen for daily activity, etc.
  • Pending a medical evaluation board, discharge from the military for medical reasons, or pending or undergoing any litigation for an injury

Outcomes

Primary Outcomes

Pain, Enjoyment, and General Activity Scale (PEG-3)

Time Frame: 6 Months

The PEG-3 measure includes 3 items evaluating 1) pain severity, and interference of pain with 2) enjoyment and 3) general activity. Response options for each item range from 0-10 with higher scores indicating higher pain intensity. The PEG-3 score is expressed as the mean of all item scores.

Secondary Outcomes

  • Time to Discontinuation of Opioids After Surgery(6 Months)

Study Sites (3)

Loading locations...

Similar Trials