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Clinical Observation on the Efficacy of Yijinjing Training in Patients with Chronic Nonspecific Low Back Pain

Clinical Observation on the Efficacy of Yijinjing Training in Patients with Chronic Nonspecific Low Back Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000411
Enrollment
Unknown
Registered
2026-02-25
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Chronic Non-Specific Low Back Pain (CNLBP)

Interventions

Treatment group:4 weeks of Yijinjing training, 5 times a week, 30 minutes each session.
Control Group:Routine physical factor therapy for 4 weeks, 3 times per week, 30 minutes each session, including 20 minutes of medium-frequency electrical therapy and 10 minutes of high-energy laser th

Sponsors

Dongzhimen Hospital of Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Meet the key points of the expert consensus for diagnosing Chinese non-specific acute and chronic low back pain; 2) No gender restrictions, aged between 20 and 60 years inclusive; 3) Have received no prior medication, non-pharmacological treatment, or surgical intervention for CNLBP within the preceding 12 weeks; 4) Have provided informed consent and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Suspected or confirmed severe spinal lesions (such as spinal fractures, syringomyelia, cauda equina syndrome, diffuse neurological disorders, etc.); 2) Individuals with severe structural deformities of the lumbar spine or a history of lumbar surgery; 3) Those diagnosed with radiculopathic or myelopathic lumbar disease; 4) Individuals with severe cardiac, hepatic, renal, or other organ diseases unsuitable for moderate-intensity exercise; 5) Pregnant women, cancer patients, or those with other serious medical conditions; 6) Individuals unable to cooperate with examination procedures (e.g., presence of metallic implants precluding MRI scans); 7) Individuals with balance dysfunction; 8) Participants currently enrolled in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Pain Visual Analog Scale;

Secondary

MeasureTime frame
Quebec Low Back Pain Disability Scale;Hip muscles surface electromyography;Multifidus muscle morphology;Range of Motion;

Countries

China

Contacts

Public ContactGu Xiaolei

Dongzhimen Hospital of Beijing University of Chinese Medicine

philguu@163.com17602294160

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026