Trigger Point Dry Needling vs Trigger Point Dry Needling With Intramuscular Electrical Stimulation
Sub-acute and Chronic Low Back Pain
About this trial
This is an interventional treatment trial for Sub-acute and Chronic Low Back Pain focused on measuring dry needling, electrical stimulation, E-Stim, LBP, low back pain, trigger point, chronic, subacute
Eligibility Criteria
Inclusion Criteria:
- 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)
Exclusion Criteria:
- 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
Sites / Locations
- William BAMC
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Treatment group 1
Treatment Group 2
In this group participants will receive trigger point dry needling with electrical stimulation first and receive trigger point needling by itself second. Only MYOTECH dry needles will be used in this study. However we are not studying the equipment.
In this group the participants will receive trigger point dry needling first and receive trigger point dry needling with electrical stimulation second. Only MYOTECH dry needles and ESTIM II dual channel stimulator will be used in this study. However we are not studying the equipment.