Perspectives on Spinal Manipulative Therapy for Low Back Pain
- Conditions
- Low Back Pain
- Interventions
- Other: Physical therapist providerOther: Physical therapy
- Registration Number
- NCT06590116
- Lead Sponsor
- University of Florida
- Brief Summary
The goal of this study is to better understand how the thoughts and beliefs of patients with low back pain and their physical therapist influence how much patients benefit from physical therapy. Participants will receive physical therapy as determined by their physical therapist including spinal manipulative therapy, exercise, and education. Participants with low back pain and their physical therapists will complete forms about their thoughts and beliefs about low back pain and treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 102
- Pain between 12th rib and buttocks with or without symptoms into one or both legs, which, in the opinion of the examiner, originate from the lumbar region.
- Meets NIH Task Force criteria for chronic low back pain
- Prior surgery to the lumbosacral spine
- Currently pregnant
- Not currently receiving spinal manipulative therapy or exercise interventions from another healthcare provider such as a chiropractor or massage therapist.
- No neurogenic signs indicating radiculopathy
- No "red flags" of a potentially serious condition (e.g., cauda equina syndrome, fracture, cancer, infection, etc.)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Physical therapists Physical therapist provider Physical therapists treating enrolled patients Patients Physical therapy Patients seeking physical therapy for low back pain
- Primary Outcome Measures
Name Time Method PROMIS-29 Baseline and 2 weeks and 6 weeks and 12 weeks and 18 weeks and 26 weeks Assesses pain intensity using a single item and seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social roles and activities, and sleep disturbance) using four items per domain. This will only be completed by patient participants in the study.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Florida
🇺🇸Gainesville, Florida, United States