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Biomechanical characteristics of low back pain and optimization of Tuina interventio

Not Applicable
Conditions
ow back pain
Registration Number
ITMCTR2000003395
Lead Sponsor
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Inclusion criteria for subjects without low back pain
1. Aged >= 18 years old and <= 55 years old, regardless of gender;
2. No lumbago and leg pain, no neuromuscular lesion within half a year;
3. The lumbar spine image has no protrusion, stenosis of the intervertebral space, no Schmorl nodules and lumbar rotation scoliosis;
4. There is no isthmus and crack in the lumbar spine;
5. No strenuous exercise 24 hours before the test;
6. Those who voluntarily participated in this study and signed informed consent.

Inclusion criteria for patients with low back pain
1. Aged >= 18 years old and <= 55 years old, regardless of gender;
2. Repeated history of waist and leg pain, course >= 3 months;
3. Two of the four neurological signs (muscle atrophy, motor weakness, decreased sensation and weakened radiation);
4. MRI shows that the waist 4~5, waist 5~sacral 1 are prominent;
5. Those who voluntarily participated in this study and signed the informed consent.

Exclusion Criteria

Those with any of the following conditions cannot be included in this test:
1. History of previous severe spinal trauma;
2. There are patients with spinal bone tumors, tuberculosis, osteoporosis, etc. seen by imaging;
3. Patients with severe cardiovascular or cerebrovascular, hematopoietic, digestive system and other serious diseases or mental illness;
4. People with other autoimmune diseases, allergic diseases and acute and chronic infections;
5. Women during pregnancy;
6. Those who are not suitable for MRI examination, such as those with cardiac pacemakers, nerve stimulators, metallic foreign bodies (metal implants, contraceptive rings), insulin pumps, etc.;
7. Those who participated in other clinical trials within the past 3 months.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Oswestry disability index;VAS;Neuromuscular activity;Joint mobility;SF-MPQ;
Secondary Outcome Measures
NameTimeMethod
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