Effect of Distal Needling on Knee Pain Using Acupuncture Techniques
Study Details
Study Description
Brief Summary
The purpose of this study is to test if specific therapeutic benefits of acupuncture are mostly attributable to contextual and psychosocial factors, such as patients' beliefs and expectations.The investigators propose using the 2 acupuncture methods, which refrains from inserting needles in the affected area, in order to evaluate the short-term and long-term efficacy of acupuncture in a clinical setting compared with placebo and compared with invasive needling that does not adhere to "correct" acupuncture rules.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
The main novel features of this study:
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First aim to assess the effect of distal needling on knee pain
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Second aim to directly compare two acupuncture techniques, placebo, needling at "wrong" places and "correct" needling for knee pain
Advantages of the study compared to published data:
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Distal needling - enables assessment of range of motion (ROM) and pain level during needling.
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Both acupuncture systems rely on minimal questioning, which simplifies the patient-practitioner interactions.
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Exploratory studies in the clinic of DP show that it is possible to distinguish between "correct" and "incorrect" needling, at least in the short term. Long term effects have not been assessed yet.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Active Comparator: deep needle non-site specific
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Device: Pain relief by Acupuncture needle at non-specific site
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Active Comparator: contralateral elbow to the knee pain
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Device: Acupuncture needle
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Active Comparator: Energy of Living Systems Needling
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Device: Acupuncture needle
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Placebo Comparator: Sham acupuncture
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Device: Acupuncture needle
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Outcome Measures
Primary Outcome Measures
- Effect of Distal Needling on Knee Pain Using Acupuncture Techniques [2 years]
Effect of Distal Needling on Knee Pain Using 4 different Acupuncture Techniques by: Pain measurement by Visual Analogue Scale (VAS) Range of motion (ROM)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Adult patients (> 18 years old), suffering chronic stable pain score >40 mm on 100 mm VAS of the knee due to patellar tendonitis.
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Patients have had X-rays or other tests confirming they are not candidates for surgery nor are scheduled for steroid injections or hyaluronic acid injections within 8 weeks from the beginning of the study.
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Adult patients (> 18 years old), two weeks after ACL reconstruction surgery (with or without meniscal involvement), with pain score >40 mm on 100 mm VAS of the knee (all patients at this stage have significant ROM limitation).
Exclusion Criteria:
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Patient refusal
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Soldiers
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Pregnancy
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Morbid obesity
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Diabetes
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Peripheral vascular disease
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Lower limb neurological deficit (such as multiple sclerosis, nerve palsy), other serious co-morbidity (including severe back pain or hip pain)
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A history of prolonged or current steroid use
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Received hyaluronic acid injections within the previous 3 months
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Have needle phobia or allergy to sticking plaster.
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Hadassah Medical Organization | Jerusalem | Please Select | Israel | 91120 |
Sponsors and Collaborators
- Hadassah Medical Organization
Investigators
- Principal Investigator: Elyad Davidson, MD, Hadassah Medical Organization
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 007212-HNO-CTIL