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Study on the synergistic mode of action of key muscle groups in lumbar intervertebral disc herniation and the mechanical mechanism of precise intervention with Tuina

Study on the synergistic mode of action of key muscle groups in lumbar intervertebral disc herniation and the mechanical mechanism of precise intervention with Tuina

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074135
Enrollment
Unknown
Registered
2023-07-31
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Lumbar disc herniation

Interventions

No low back pain:NA
Lumbar disc herniation:NA

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for subjects without low back pain (1) Age =18 years and =55 years, gender is not limited; (2) No low back pain or neuromuscular lesions within six months; (3) No herniation, intervertebral space stenosis, Schmidt's nodes or lumbar rotational scoliosis on lumbar spine imaging; (4) No isthmic fissure or occult fissure in the lumbar spine; (5) No strenuous exercise 24 hours before the test; (6) Those who voluntarily participated in this study and signed an informed consent form. 2. Inclusion criteria for patients with lumbar disc herniation (1) Age =18 years and =55 years, gender is not limited; (2) Meet the diagnostic criteria for lumbar disc herniation; (3) Repeated history of lumbar and leg pain with a duration of =6 weeks; (4) MRI showed lumbar 4-5 and lumbar 5-sacral 1 disc herniation; (5) Those who voluntarily participated in this study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: Persons with one of the following conditions cannot be included in this trial: 1 A history of prior severe spinal trauma and spinal surgery; 2 With severe neurologic deficits such as cauda equina syndrome; 3 Patients with spinal stenosis, spinal bone tumors, tuberculosis, osteoporosis, etc. as seen on imaging; 4 Patients with a combination of cardiovascular, cerebrovascular, hematopoietic, digestive system and other serious diseases or mental illness; 5 Patients with other autoimmune diseases, allergic diseases and acute or chronic infections; 6 Women during pregnancy; 7 Those who are not suitable for MRI, such as those with cardiac pacemakers, neurostimulators, metal foreign bodies (metal implants, contraceptive rings), insulin pumps, etc; 8 Those who have participated in other clinical trials within the last 3 months.

Design outcomes

Primary

MeasureTime frame
Oswestry disability index;

Secondary

MeasureTime frame
VAS;SF-MPQ;Assessment of flexural relaxation phenomena;Rapid arm lift test;Joint angles for functional movement testing;Joint moments for functional movement testing;Synergistic activation of lumbar, pelvic, and lower extremity muscle groups;

Countries

China

Contacts

Public ContactXin Zhou

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Chinese Medicine

zxzxzxzhouxin@163.com+86 189 3090 1005

Outcome results

None listed

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