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Clinical Observation of Transcranial Direct Current Stimulation Combined with Rehabilitation Therapy on Functional Improvement in Knee Osteoarthritis

Clinical Observation of Transcranial Direct Current Stimulation Combined with Rehabilitation Therapy on Functional Improvement in Knee Osteoarthritis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089958
Enrollment
Unknown
Registered
2024-09-20
Start date
2023-11-10
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

knee osteoarthritis

Interventions

Experimental group:Conventional rehabilitation therapy + tDCS
Control group:Conventional rehabilitation therapy

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for KOA: Refer to the "Osteoarthritis Diagnosis and Treatment Guidelines" , with chronic pain as the main clinical symptom (VAS score = 3 points); 2.K-L grading of grade I-III, with no large loose bodies in the joint based on X-ray findings; 3.No relevant treatment received in the week prior to participation in this clinical trial, and no participation in other clinical trials in the past month; 4.Informed consent obtained from the patient and their family, and ability to comply with treatment and observation, as evidenced by signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with knee joint pain not primarily due to KOA; 2.Patients with severe swelling in the knee joint, making assessment and exercise training difficult; 3.Patients with severe heart, brain, liver, kidney, hematologic disorders, or mental illness; 4.Patients with knee joint infection, open wounds, tumors, tuberculosis, or related rheumatologic immune system disorders; 5.Patients with a history of knee joint surgery or internal metallic implants; 6.Individuals with damaged skin at the site of stimulation or sensitivity to electrical currents.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale (VAS);Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC);The three-dimensional gait;Surface electromyography of the lower extremities;The human body's balance indicators;Knee Injury and Osteoarthritis Outcome Score;

Secondary

MeasureTime frame
Lequesne Index;Short Form Health Survey SF-36;"Timed Up and Go" Test (TUGT);

Countries

China

Contacts

Public ContactJun Xing

The First Hospital of Hebei Medical University

56901734@hebmu.edu.cn+86 186 3388 9905

Outcome results

None listed

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