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A randomized controlled clinical study on the intervention of Yijinjing in lumbar disc herniation during rehabilit

A randomized controlled clinical study on the intervention of Yijinjing in lumbar disc herniation during rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000885
Enrollment
Unknown
Registered
2025-05-01
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

lumbar disc herniation

Interventions

Control group:Tuina + NASS-Recommended Exercise
Treatment group:Tuina + Yijinjing exercise

Sponsors

Longhua Hospital Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1 meet the diagnostic criteria; 2 age between 18 and 60 years old 3. VAS score > 0 and < 4 4. Did not participate in other clinical trials; 5. Sign informed consent agree and cooperate with relevant treatment.

Exclusion criteria

Exclusion criteria: 1. Lumbar disc herniation patients with surgical indications or lumbar surgery; 2. Patients with fractures bone diseases lumbar spondylolisthesis disc herniation and other diseases through imaging examination; 3. Patients who are pregnant or preparing for pregnancy; 4. Patients with severe primary diseases such as liver kidney hematopoietic system endocrine system cardiovascular and cerebrovascular system nervous system rheumatism and immunity tuberculosis vertebral deformities tumors mental diseases and postoperative patients; Suspected sedative hypnotics opioid analgesics and alcohol abuse history; Patients with skin diseases and infectious diseases; 5. Patients with severe osteoporosis; 6. Patients with mental disorders language disorders motor dysfunction and mental illness; 7 the condition is critical it is difficult to make an exact assessment of the effectiveness and safety of treatment. 8. Patients who are not suitable or can not apply this treatment for other reasons.

Design outcomes

Primary

MeasureTime frame
Oswestry Disability Index (ODI);

Secondary

MeasureTime frame
Local tissue hardness;Lumbar motion;visual analogue scale;12-item Short Form Health Survey Version 2;

Countries

China

Contacts

Public ContactYe Jie

Longhua Hospital Shanghai University of Traditional Chinese Medicine

yejie1977@126.com+86 13301880301

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026