NCT Number: NCT00035399
Efficacy of Acupuncture With Physical Therapy for Knee Osteo-Arthritis
This study will examine the efficacy of acupuncture in combination with exercise physical therapy for moderate osteoarthritis (OA) of the knee.
Looking for future studies?
Notify MeKey information
Conditions
Age range
40 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Penn Therapy and Fitness, Philadelphia, Pennsylvania, United States
About this study
Acupuncture is an ancient Chinese technique of using a fine needle to stimulate points along theoretical meridians of energy to correct imbalances thought to be responsible for specific disease states. In the United States, acupuncture is often used for the treatment of painful conditions. The 1997 NIH Consensus Conference concluded that there was adequate evidence of efficacy in an acute dental pain model and in nausea. In chronic pain, most studies were too small, poorly designed, poorly executed, or improperly controlled to adequately demonstrate that needle acupuncture worked better than sham acupuncture, placebo, standard medical therapy, or even no treatment. Osteoarthritis (OA) of the knee has been proposed as a good model to test the efficacy of acupuncture in a chronic pain condition because it is an extremely common, well defined, and disabling condition with well established outcome measures for symptoms and functional status. There is clinical trial evidence of efficacy for the standard treatments of acetaminophen and NSAIDs, and exercise physical therapy (EPT), which is usually added when the patient develops functional limitations. One high quality study of acupuncture for knee OA, demonstrated moderate benefit in an unblinded comparison to a usual care control group. As such, a major question remains about whether acupuncture, used in addition to exercise therapy, will provide a clinically meaningful improvement in pain and function. Since pain can be the primary limiting factor in improved exercise capacity, if acupuncture has any efficacy in reducing the pain of knee OA, then the combination with an EPT program should be substantially more effective than EPT alone. Another major concern is that the effect of the acupuncture may be predominantly mediated by non- specific placebo effects rather than the specific effects of the placement of a needle. Another important component of this proposal is our use of a validated blinded placebo needle instead of sham acupuncture points. Therefore, the primary goal of this proposal is to use a properly designed randomized blinded clinical trial, using American College of Rheumatology (ACR) criteria and Food and Drug Administration (FDA) recommended outcome measures, to determine whether the addition of acupuncture to standard EPT provides an overall clinically important benefit to patients with symptomatic knee OA compared to placebo acupuncture. As a secondary goal, we will use the clinical trial data to develop prognostic and etiologic models for the patients that are most likely to respond to acupuncture. If a clinically important benefit for acupuncture is found, a broader application of this technique would be justified. However, if the results are negative, then the addition of acupuncture to EPT should be generally curtailed.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- X-ray proven osteoarthritis of the knee - Kellgren level 2 or greater
- More than 3 months of moderate knee pain
- Previous trial of NSAIDs or acetaminophen
- Physician referral for at least 6 physical therapy treatments
- Capacity to understand the requirements of the study and complete questionnaires
- Average knee pain with movement, 4 or above, during the last week
Exclusion criteria
- Average hip, back, ankle pain is greater than average knee pain (scale 1-10)
- Back, hip or ankle pain substantially interferes with patient knee assessment
- History of gout
- Acupuncture in the last year
- Moderate or greater hip or ankle pain greater than 3 daily
- Local corticosteroid injection into the effected knee within the past 4 weeks
- Hyaluronidase within the past 6 months
- Bleeding disorder or current use of Coumadin or Heparin
- Cardiac or pulmonary disease limiting exercise tolerance enough to limit the standard exercise physical therapy
- History of alcohol or drug abuse within the past 6 months
- Unable to complete a six minute walk test
Treatment and study plan
Sponsors and collaborators
Lead sponsor
National Center for Complementary and Integrative Health (NCCIH)
Nih
Registry information
Important dates
- Study start
- 2002
- Primary completion
- 2007
- Study completion
- 2007
- First posted
- May 6, 2002
- Registry last updated
- Aug 12, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Physiological Impact of Different Types of Osteoarthritis Education.
NCT06400329
Arthritis, Chronic Pain
Hamilton, Ontario, Canada
View Trial DetailsSafety Study of HZT-501 in Patients Who Require Long-Term Daily Non-steroidal Anti-inflammatory Drug Treatment
NCT00984815
Arthritis, Arthritis, Rheumatoid
Chicago, Illinois, United States
View Trial DetailsTrial Outcomes for Massage: Caregiver-Assisted vs. Therapist-Treated
NCT03100539
Arthritis, Chronic Pain
Indianapolis, Indiana, United States
View Trial DetailsTrichomylin® Safety, Tolerability & Pharmacokinetics in Healthy Adults and First in Human Osteoarthritis Pain Evaluation
NCT04867057
Arthritis, Chronic Pain
Adelaide, South Australia, Australia
View Trial Details