non-specific low back pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ?Voluntary signing of the informed consent form; ? Age = 20 years and = 60 years; ?Meets the diagnostic criteria in the "Clinical Guidelines for the Treatment of Non-specific Low Back Pain in China" issued by the expert group of the Spinal Cord Professional Committee of the Chinese Society of Rehabilitation Medicine in 2022: stable vital signs, stable condition, disease duration of more than 12 weeks, pain and discomfort in the area below the costal margin, above the transverse gluteal line and between the mid-axillary line on both sides caused by causes other than spine specific diseases and neurogenic pain of unknown etiology. discomfort, unilateral or bilateral, with or without thigh involvement pain (above the knee), and with limitation of lumbar movement; ? A mean score of =3 on the visual analogue scale (VAS) score for low back pain in the last 7 d; ? Exclusion of osteoarthritic and spinal canal back pain lesions and absence of neurological diseases (e.g. craniocerebral injury, epilepsy) by specialist physical examination and corresponding ancillary tests (e.g. lumbar spine X-ray or MRI); ? Attended the Fifth Hospital of Guangzhou Medical University from May 22 to January 23; ? No treatment related to low back pain within the last 3 months;
Exclusion criteria
Exclusion criteria: ? compression of the sciatic nerve, with pain firing below the knee with abnormal sensation; ? history of previous surgery or lumbar spine fracture or lower extremity bone fracture, osteoarthritis of the knee and hip joints, acute disc herniation, or lower extremity muscle movement disorders; ? Patients with a history of tumors and active tumors in the lumbar region; ? having neurological disorders such as stroke, spinal cord injury, multiple sclerosis, etc.; or having musculoskeletal system injuries such as damage to bones, muscles, ligaments and soft tissue structures of the upper extremities, lower extremities, head, neck and trunk; ? Patients with severe balance and coordination dysfunction; ? Any clinical condition that may affect gait, such as musculoskeletal, neurological, or cardiopulmonary symptoms; ? Flat feet, ankle instability, excessive forward rotation of the foot, obstructed history of sagittal plane motion of the foot thumb and ankle joint; ? Suffering from critical illness, skin diseases, serious internal diseases, etc; ? Having participated in strenuous exercise within 24h prior to the test; ? Patients who had received back treatment prior to the test; ? Pregnancy status or patient pregnancy during the observation period requires withdrawal from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 3D gait analysis;Foot pressure test;Far infrared thermal imaging analysis; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual Analogu Scale;Oswestry Dysfunction Index Questionnaire (ODI); | — |
Countries
China
Contacts
The Fifth Affiliated Hospital of Guangzhou Medical University