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Electroacupuncture versus Exercise in Patients with Knee Osteoarthritis: A Randomized Controlled Trial

Electroacupuncture versus Exercise in Patients with Knee Osteoarthritis: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070376
Enrollment
Unknown
Registered
2023-04-11
Start date
2023-04-12
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Osteoarthritis of knee

Interventions

exercise group:exercise treatment
electroacupuncture group:electroacupuncture

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients will be eligible if they : (I) aged 45-75, any gender; (2) meet the American College of Rheumatology (ACR) diagnostic criteria of KOA; (3) have knee pain for more than 3 month; (4) have radiological examination within 6 months indicating II or III in Kellgren-Lawrence grade with medial more than lateral tibiofemoral osteoarthritis in at least one knee; (5) score 4 or greater in numerical rating scale (NRS) during flat walking for the past week; (6) are willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: Patients will be ineligible if meet the following points: (1) history of knee surgery for the evaluating knee or waiting for any surgery for either knee; (2) knee pain due to other diseases (eg meniscus tear, rheumatoid arthritis, joint cavity infection, malignancy, gout, lumbosacral diseases with symptom of lower extremity, etc.); (3) arthroscopy history within 1 year or intraarticular injection history within 6 months for the evaluating knee; (4) either knee received acupuncture/exercise therapy for the last 6 months; (5) severe acute or chronic organic or neuropsychiatric disorder; (6) disorders of coagulopathy (eg hemophilia); (7) pacemakers or epilepsy; (8) pregnancy preparation, pregnant or lactation period; (9) participated in other clinical studies within the past 1 month.

Design outcomes

Primary

MeasureTime frame
changes in numerical rating scale;Osteoarthritis Outcome Score (KOOS) Function in daily living (ADL);

Secondary

MeasureTime frame
patient's global assessment (PGA);Knee injury and Osteoarthritis Outcome Score (KOOS) Pain;KOOS knee-related Quality of Life (QOL);Credibility/Expectancy Questionnaire;30-second Chair Stand Test (30s-CST);40m (4x10m) Fast Paced Walk Test (40m FPWT);Daily Physical Activity level (DPA);Short Form 6 Dimensions (SF-6D);Five-level EuroQol five-dimensional questionaire (EQ-5D-5L);rescue medicine;adverse event;

Countries

P.R.China

Contacts

Public ContactLin Jianhao;Liu Cunzhi

Peking University People's Hospital; School of Acupuncture-Moxibustion and Tuina, Beijing University of Chinese Medicine

linjianhao@pkuph.edu.cn+86 10 88326250;+86 10 53912201

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026