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Transcranial Electrical Stimulation and Electroacupuncture in Knee Osteoarthritis: An fMRI Study

Transcranial Electrical Stimulation and Electroacupuncture in Knee Osteoarthritis: An fMRI Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000273
Enrollment
Unknown
Registered
2026-02-03
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Knee osteoarthritis

Interventions

Electroacupuncture Group:Electroacupuncture
tDCS Group:Transcranial Electrical Stimulation
Combination Therapy Group:Transcranial Electrical Stimulation Combined with Electroacupuncture
Healthy Control:None

Sponsors

Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
38 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Bilateral KOA meeting the above diagnostic criteria, right-handed, regardless of gender, aged 38–75 years, with an educational level of junior high school or above; 2. Visual Analogue Scale (VAS) score = 3 and = 7; 3. No history of neurological or psychiatric disorders; 4. Participants or their relatives are aware of the study protocol, agree to participate, and sign relevant documents such as the "Informed Consent Form."

Exclusion criteria

Exclusion criteria: 1. Patients with other chronic pain conditions, such as myofascial strain, cervical spondylosis, intervertebral disc herniation, postherpetic neuralgia, or periarthritis of the shoulder; 2. Patients with indications for knee joint surgery, such as significant narrowing of the knee joint space, intra-articular loose bodies, or fractures; 3. Patients with accompanying conditions including tumors, rheumatic arthritis, rheumatoid arthritis, gout, tuberculosis, or suppurative infections; 4. Patients who have used any anti-inflammatory or analgesic medications within the past week; 5. Patients with skin diseases or secondary infections around the joint area; 6. Pregnant or lactating women, or patients with chronic diseases such as hypertension or diabetes; 7. Patients with a history of major illnesses, head trauma, neuropsychiatric disorders, or other conditions that may affect brain activity; 8. Patients with cognitive impairment, defined as a Mini-Mental State Examination (MMSE) score < 27; 9. Patients with contraindications to magnetic resonance imaging (including claustrophobia); 10. Patients who refuse to sign the Informed Consent Form.

Design outcomes

Primary

MeasureTime frame
VAS Score;HAMA Score;

Secondary

MeasureTime frame
Low-frequency amplitude;Regional Homogeneity;Functional Connectivity;Degree Centrality;

Countries

China

Contacts

Public ContactXie Hongwu

Second Affiliated Hospital of Nanchang University

xiehongwu361@163.com18170089285

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026