Chronic Non-Specific Low Back Pain
Conditions
Interventions
Combination group:The combination group received an intervention combining trigger point manual pressure release therapy and Pilates apparatus group training
Manual therapy group:The manual therapy group received trigger point manual pressure release therapy
Training group:The training group received Pilates apparatus group training
Sponsors
Rehabilitation Hospital Affiliated to Chongqing Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Meeting the diagnostic criteria for chronic non-specific low back pain (pain duration exceeding 12 weeks, no radiating pain in the lower limbs or sensory impairments in the limbs, no abnormalities on imaging examinations, etc.), with clinical diagnoses such as lumbar muscle strain or lumbar fascial inflammation; female, aged 18–60 years; Visual Analogue Scale (VAS) score >= 3; signed informed consent and able to cooperate with post-trial follow-up; capable of cooperating with interventions and functional assessments; and no receipt of any interventions related to chronic non-specific low back pain within the two weeks prior to participation in the trial.
Exclusion criteria
Exclusion criteria: 1. Exclusion of certain types of non-specific low back pain (e.g., sacroiliac joint pain, lumbar facet joint dysfunction syndrome, lumbar discogenic pain, interspinous/supraspinous ligamentitis, piriformis syndrome, superior cluneal nerve entrapment syndrome); 2. exclusion of specific low back pain (e.g., lumbar disc herniation, paravertebral infection or tumor-related back pain, visceral referred back pain, back pain due to spinal fracture, dislocation, surgery, congenital spinal deformities, ankylosing spondylitis, etc., as well as pregnant or lactating women); 3. exclusion of individuals with other severe diseases (e.g., severe cardiac, pulmonary, renal, or other systemic diseases that preclude tolerance for rehabilitation training).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale (VAS) ;Oswestry disability Index(ODI);Clinical efficacy evaluation; | — |
Countries
China
Contacts
Public ContactLi Lingang
Rehabilitation Hospital Affiliated to Chongqing Medical University
Outcome results
None listed