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Clinical study on the effect of warm balneotherapy on pain function and biomechanics in patients with cold-damp paralytic obstruction type of knee osteoarthritis

Clinical study on the effect of warm balneotherapy on pain function and biomechanics in patients with cold-damp paralytic obstruction type of knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000416
Enrollment
Unknown
Registered
2024-09-11
Start date
2024-09-13
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:Health education programmes are used and water baths are not administered
Experimental group:Using 40 ± 2 ? warm water immersion in the affected knee knee joint (thermometer monitoring) each immersion 30min every other day 3 times a week a total of 12 weeks of treatment

Sponsors

Shuguang Hospital affiliated to Shanghai University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria of knee osteoarthritis and the criteria of cold-damp paralytic obstruction type; (2) Age 50-80 years old, gender is not limited; (3) At least one of the five items of WOMAC pain score is 40 or above at the time of enrollment; (4) Those who voluntarily serve as test subjects and are able to accept the trial protocol and ensure completion of the course of treatment. (5) Can walk independently without assistance; (6) Have a stride length of more than 50cm; (7) Can complete proprioceptive testing independently without assistance; (8) Have a bath at home for warm water bath therapy.

Exclusion criteria

Exclusion criteria: (1) Persons with a combination of serious primary diseases such as cardiovascular, hepatic, renal and hematopoietic systems; (2) People with allergies or those who are allergic to multiple drugs; (3) Patients with mental illness or senile dementia; (4) Those who do not cooperate with the treatment and do not follow the prescribed program; (5) Those who have skin injury or skin disease in the treatment area; (6) People with abnormal skin temperature sensation; (7) Those who are participating in other drug clinical trials or have participated in other clinical trials within three months; (8) Patients who must wear a lumbar support or other items that affect the adhesion of reflective light markers for gait analysis when walking or standing.

Design outcomes

Primary

MeasureTime frame
Western Ontario and McMaster Universities Osteoarthritis Index;

Secondary

MeasureTime frame
Proprioception test results;Muscle tone test results;Gait analysis test results;

Countries

China

Contacts

Public ContactBo Chen

Shuguang Hospital Affiliated to Shanghai University of TCM

cbm818@126.com18516526835

Outcome results

None listed

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