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Clinical Application and Mechanical Effect of Tuina Intervention on Hip-Knee-Ankle Kinematic Chain in Lower Limbs of Knee Osteoarthritis

Clinical Application and Mechanical Effect of Tuina Intervention on Hip-Knee-Ankle Kinematic Chain in Lower Limbs of Knee Osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000293
Enrollment
Unknown
Registered
2024-08-24
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Knee Osteoarthritis

Interventions

control group:conventional treatment
Intervention group:Tuina combined with conventional treatment

Sponsors

Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for KOA patients were as follows: 1)The average pain score in WOMAC was=4; 2)The lower limb length X-ray showed abnormal lower limb line; 3)Age 20-65 years old male or female; 4)No other treatment that may interfere with the results of this study has been received in the past 4 weeks; 5)Accords with the above conditions will be included in patients with unilateral KOA. Inclusion criteria for healthy volunteers were as follows: 1) Age between 20 and 65 years old male and female; 2) healthy body no previous history of lower extremity nervous system and musculoskeletal system diseases; 3) correctly understand the requirements of the researchers actively cooperate to complete the test and voluntarily sign the informed consent.

Exclusion criteria

Exclusion criteria: 1)Patients with severe bone and joint diseases, such as rheumatoid arthritis, rheumatoid arthritis, osteoporosis, gout, etc. An active knee infection in the past 12 months. 2)Patients with cardiovascular, cerebrovascular, liver, kidney, hematopoietic, digestive or mental illness, or other conditions that cause more restriction or pain in activities such as sitting, standing, or walking than KOA. 3)Pregnant and lactating women who could not complete the radiological examination. 4)Patients who cannot correctly understand and complete research related to various scales and informed patient consent. 5)Patients who do not wish to participate in the study/other conditions that the investigator considers inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
WOMAC;

Secondary

MeasureTime frame
TSK-17;Functional Movement Screen;Key Symptoms and Signs/TCM Syndrome Classification Quantitative Evaluation of KOA;the Timed Up and Go;Weight Bearing Lunge Test;

Countries

China

Contacts

Public ContactWen Zonglin

Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine

shuguangtuinawzl@163.com18818273239

Outcome results

None listed

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