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Study on the efficacy of SHI’s Qiang Jin exercise on lumbosacral multifidus muscles

Study on the efficacy of SHI’s Qiang Jin exercise on lumbosacral multifidus muscles

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068836
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic nonspecific low back pain

Interventions

control group:behavior management
Intervention group:SHI's Qiang Jin Exercise + behavior management

Sponsors

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shi’s Center of Orthopedics and Traumatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. In line with the diagnostic criteria of chronic nonspecific low back pain (the diagnostic criteria of Chinese Association for the Study of Pain (CASP) (the 2018 edition)) 2. Aged 18-65 years. None gender limitations. 3. To be able to understand the possible accidents and risks in the process of exercise, and who voluntarily participate in this study and sign the "informed consent".

Exclusion criteria

Exclusion criteria: (1) Patients diagnosed with specific low back pain by examinations, including fracture, tumor, disc herniation, spinal stenosis, lumbar thrust-slip, tuberculosis, etc; (2) Patients diagnosed with specific disorders affecting the lumbar spine; (3) Patients with low back pain that extends into the leg, usually below the knee (radicular pain) result from mechanical nerve root compression. (4) Patients with cardiovascular, cerebrovascular, hematopoietic, digestive system and other serious diseases or mental illness; (5) Pregnant and lactating women or patients with severe impairment of heart, liver and kidney function; (6) Other autoimmune diseases, allergic diseases, acute and chronic infections; (7) Those who are unwilling to join the experiment or currently participating in other clinical trials or Other circumstances considered inappropriate by the researcher to participate in the study;

Design outcomes

Primary

MeasureTime frame
visual analogue scale;

Secondary

MeasureTime frame
Oswestry Disability Index;ultrasound imaging in measuring the multifidus muscle size and elastography;changes of multifidus net area and T2 signal ratio in MRI measurement;

Countries

China

Contacts

Public ContactXiang Wang

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

w8x@163.com+86 138 1698 5219

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 8, 2026