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The biomechanical mechanism based on gait analysis to explore the application and popularization value of fitness Qigong mawangdui guidance in the prevention and treatment of non-specific low

Phase 1
Conditions
onspecific low back pain
Registration Number
ITMCTR2200005605
Lead Sponsor
Hospital of Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

245/5000
(1) patients who can meet NLBP diagnostic criteria;

(2) Patients aged 18 and above;

(3) pain originated from somatic referred pain or non-root pain (above the knee);

(4) Participants who know the relevant information of this study and are willing and have completed the relevant informed consent;

(5) Use of a medically approved contraceptive method (such as an intrauterine device, birth control pill or condom) during the study period and for 3 months after the study period for women of non-surgical sterilization or childbearing age; The serum or urine HCG test of female patients of childbearing age who were not undergoing surgical sterilization must be negative within 72 hours prior to study enrollment. And must be non lactation period; For male patients whose partners are women of reproductive age, effective methods of contraception should be used during the trial.

Exclusion Criteria

(1) Patients under the age of 18;

(2) specific low back pain (tumor, infection, metabolic disease, rheumatoid arthritis, fracture);

(3) spinal deformity (spondylolisthesis, spondylolysis or scoliosis);

(4) Pain below the knee;

(5) diseases outside the spinal cord (such as vascular and urogenital diseases);

(6) Have a history of lumbar surgery;

(7) there are root symptoms;

(8) low back pain with 2 or more other parts of the pain;

(9) pregnancy.

(10) Patients with substantial damage to other important organs, such as severe heart, liver, kidney, lung dysfunction and cardiovascular and cerebrovascular diseases;

(11) Patients prone to infection and bleeding, tumors, and postoperative dysfunction;

(12) Patients who have received traditional Chinese medicine treatment such as acupuncture, massage, application and fumigation in the past 3 months;

(13) persons with previous mental illness or long-term use of sedatives;

(14) Patients who cannot complete basic treatment and have poor compliance;

(15) Incomplete data affect the assessment of curative effect or cannot determine curative effect;

(16) Withdrawal by oneself due to adverse reactions that are difficult to tolerate.

(Note: Patients meeting any of the above criteria are excluded)

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Musculoskeletal ultrasound related parameters;Parameters related to plantar pressure;Gait kinematics related parameters;
Secondary Outcome Measures
NameTimeMethod
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