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Acupuncture Therapy for Knee Osteoarthritis

Efficacy of Acupuncture Therapy Versus Sham Acupuncture on Knee Osteoarthritis: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03366363
Acronym
ATKOA Ⅱ
Enrollment
480
Registered
2017-12-08
Start date
2017-12-15
Completion date
2019-06-30
Last updated
2017-12-08

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

Conditions

Knee Osteoarthritis

Keywords

Knee osteoarthritis, acupuncture, electroacupuncture, sham acupuncture

Brief summary

Knee osteoarthritis (KOA), also called degenerative knee disease, is one of the most common bone and joint diseases in clinic. It was estimated to affect more than 9 million individuals in the United States in 2005 and is a leading cause of disability and medical costs. Most elderly people over the age of 65 have radiographic and/or clinical evidence of osteoarthritis. KOA is a lifelong disease which can lead to obvious pain, joint stiffness, limitation of activity and even joint failure or disability. Acupuncture is a popular treatment taken from ancient Chinese medicine, in which fine needles are placed into the body at specific points. Studies have shown that acupuncture can stimulate nerves under the skin, causing the body to produce natural pain-relieving substances (endorphins). However the evidences of acupuncture for KOA are contradictory. According to the review, intensive acupuncture with three sessions a week is more effective for KOA than sparse acupuncture with one session a week. Moreover, the papers published in the past years suggest that manual acupuncture and electro-acupuncture are most commonly used acupuncture therapy for the treatment of knee osteoarthritis. The aim of this study is to evaluate the efficacy of intensive electro-acupuncture or manual acupuncture versus sham acupuncture in reducing pain and improving function in patients with KOA.

Interventions

OTHERacupuncture

acupuncture is a therapy of traditional Chinese medicine,in which acupuncturist puncture the patient's skin at specific acupoints with needle.

Sponsors

Beijing science and technology commission
CollaboratorUNKNOWN
Beijing Hospital of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Acupuncturist (Electro-acupuncture group and Manual acupuncture group), Participant, Outcome Assessor

Eligibility

Sex/Gender
ALL
Age
45 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age 45-75 years old, male or female 2. Single / bilateral knee pain, duration of more than 6 months 3. KL (Kellgren-Lawrence) grade Ⅱ or Ⅲ 4. NRS ≥ 4

Exclusion criteria

1. Surgery history of knee or waiting for surgery (knee replacement or knee arthroscopy) 2. Knee pain caused by other diseases (such as joint bodies, severe effusion of joint cavity, infection, malignant tumors, autoimmune diseases, trauma, fracture, gout, lumbosacral vertebrae disease, etc.) 3. History of arthroscopy within 1 year or intra-articular injection within 4 months 4. History of receiving acupuncture or massage treatment within 3 months 5. Severe acute/chronic organic or mental diseases 6. Coagulation disorders (such as hemophilia, etc.) 7. Cardiac pacemaker, metal allergy or needle phobia 8. Pregnant women, pregnant and lactating women 9. Participation in another clinical study in the past 3 months

Design outcomes

Primary

MeasureTime frameDescription
Response rate8 weeksthe percentage of patients with improvement in average pain (numerical rating scale, NRS) at least 2 units and in Western Ontario and Mcmaster Universities Osteoarthritis Index (WOMAC) function subscale score at least 6 units at 8 weeks. Pain NRS was a self-administered instrument, a number selected from 0-10 by participant. Intensity of pain range (over past week): 0 =no pain to 10 =worst possible pain. Higher score indicating severe pain. The WOMAC function subscale referred to the participant's ability to move around and perform usual activities of daily living. The WOMAC function subscale was comprised of 17 questions regarding the degree of difficulty experienced due to OA in the study knee. The WOMAC function subscale score for each question ranged from 0 (minimum) to 4 (maximum), higher scores signified worse physical function. An overall score range of 0 (minimum) to 68 (maximum), with higher scores indicating worse physical function.

Secondary

MeasureTime frameDescription
Knee-joint painbaseline, 8 weeks, 16 weeks and 26 weeksusing numerical rating scale (NRS). NRS was a self-administered instrument, a number selected from 0-10 by participant. Intensity of pain range (over past week): 0 =no pain to 10 =worst possible pain. Higher score indicating severe pain.
Knee-joint functionbaseline, 8 weeks, 16 weeks and 26 weeksusing WOMAC function subscale. The WOMAC function subscale referred to the participant's ability to move around and perform usual activities of daily living. The WOMAC function subscale was comprised of 17 questions regarding the degree of difficulty experienced due to OA in the study knee. The WOMAC function subscale score for each question ranged from 0 (minimum) to 4 (maximum), higher scores signified worse physical function. An overall score range of 0 (minimum) to 68 (maximum), with higher scores indicating worse physical function.
Knee-joint stiffnessbaseline, 8 weeks, 16 weeks and 26 weeksusing WOMAC stiffness subscale. The WOMAC stiffness subscale was comprised of 2 questions regarding the degree of stiffness experienced in the study knee. The WOMAC stiffness subscale score for each question ranged from 0 (minimum) to 4 (maximum), higher scores signified worse stiffness. An overall score range of 0 (minimum) to 8 (maximum), with higher scores indicating more stiffness.
Quality of lifebaseline, 8 weeks, 16 weeks and 26 weeksusing 12-Item Short Form Health Survey. An overall score range of 0 (minimum) to 100(maximum), with higher scores indicating better quality of life.
Response rate16 weeks, 26 weeksthe percentage of patients with improvement in average pain (numerical rating scale, NRS) at least 2 units and in Western Ontario and Mcmaster Universities Osteoarthritis Index (WOMAC) function subscale score at least 6 units at 16 and 26 weeks. Pain NRS was a self-administered instrument, a number selected from 0-10 by participant. Intensity of pain range (over past week): 0 =no pain to 10 =worst possible pain. Higher score indicating severe pain. The WOMAC function subscale referred to the participant's ability to move around and perform usual activities of daily living. The WOMAC function subscale was comprised of 17 questions regarding the degree of difficulty experienced due to OA in the study knee. The WOMAC function subscale score for each question ranged from 0 (minimum) to 4 (maximum), higher scores signified worse physical function. An overall score range of 0 (minimum) to 68 (maximum), with higher scores indicating worse physical function.
Expectancy score1 week(after the first treatment)using Credibility/expectancy questionnaire
Blinding assessment4 weeks and 8 weeksBlinding assessment will be performed in all 9 centers
Global effect8 weeks, 16 weeks and 26 weeksOverall Treatment Effect (extremely improved, slightly improved, not changed, slightly aggravated, extremely aggravated)
Adverse eventsfirst treatment up to 8 weeksAdverse Event Form
Credibility score1 week(after the first treatment)using Credibility/expectancy questionnaire

Countries

China

Contacts

Primary ContactCun-Zhi Liu
lcz623780@126.com0086-10-52176043
Backup ContactJian-Feng Tu
tujianfeng1@126.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026