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Perspectives on Spinal Manipulative Therapy for Low Back Pain

Not Applicable
Active, not recruiting
Conditions
Low Back Pain
Interventions
Other: Physical therapist provider
Other: 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
Inclusion Criteria
  • 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
Exclusion Criteria
  • 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
GroupInterventionDescription
Physical therapistsPhysical therapist providerPhysical therapists treating enrolled patients
PatientsPhysical therapyPatients seeking physical therapy for low back pain
Primary Outcome Measures
NameTimeMethod
PROMIS-29Baseline 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
NameTimeMethod

Trial Locations

Locations (1)

University of Florida

🇺🇸

Gainesville, Florida, United States

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