Trigger Point Dry Needling vs Trigger Point Dry Needling With Intramuscular Electrical Stimulation
- Conditions
- Sub-acute and Chronic Low Back Pain
- Registration Number
- NCT03539588
- Lead Sponsor
- William Beaumont Army Medical Center
- Brief Summary
trigger point dry needling with intramuscular electrical stimulation vs trigger point dry needling
- Detailed Description
The purpose of this study is to evaluate if trigger point dry needling with intramuscular electrical stimulation is more effective in decreasing pain and disability in individuals with sub-acute and chronic low back pain (LBP) than with trigger point dry needling alone. The investigators are using a within subjects randomized crossover study that will recruit 30 active duty military personnel or beneficiaries from William Beaumont Army Medical Center and all associated clinics. The investigators hypothesize that individuals with LBP will exhibit larger improvements in pain and disability when receiving trigger point dry needling with intramuscular electrical stimulation than when receiving trigger point dry needling alone.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- Currently experience low back pain for greater than 4 weeks (Low back pain defined as pain below the T12th vertebrae with or without radiation) Military or DOD Beneficiary (any branch; 18-65 years of age)
- Structural Deformity (ankylosing Spondylitis, Scoliosis)
- Has any other Orthopedic condition that may keep subject from performing Low - Back Exercises
- Tumors
- Spinal infection or local infection
- Pregnancy-All female subjects will be given either a blood serum or urine pregnancy test.
- Spinal cord compression or Cauda Equina Syndrome
- Subject with the inability to keep appointments
- Has History of prior surgery
- Has received Dry Needling or Acupuncture in the last 6 months
- History of bleeding disorders
- High anti-coagulant use
- History of immune suppression
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Numeric Pain Rating Scale to assess change Baseline and before and after each treatment session, duration per subject is approximately 3 weeks an 11 point scale on which the participant will grade their pain
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
William BAMC
🇺🇸El Paso, Texas, United States
William BAMC🇺🇸El Paso, Texas, United States