Simple calf massage may ease knee arthritis pain, small trial hopes
NCT ID NCT07507175
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a hands-on technique called gastrocnemius myofascial release (a type of calf muscle massage) can reduce pain and improve physical function in women aged 45-55 with knee osteoarthritis. Thirty participants will receive either the real treatment or a sham version three times a week for four weeks. The goal is to see if adding this simple therapy to standard care helps with pain, walking, and daily activities.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- gastrocnemius myofascial release (a manual therapy technique applied to the calf muscle)
- What this could lead to
- If it works, this could offer a simple, non-drug way to ease knee pain and improve walking and daily activities for women with knee osteoarthritis.
- What could go wrong
- This is a small, early-stage trial with only 30 participants. The treatment is a hands-on technique, so results may vary and may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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45 to 55 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients' ages ranged between 45 and 55 years . * BMI ≤35 * Patients with a diagnosis of primary KOA according to the American College of Rheumatology classification at the screening visit . * Onset of symptomatic knee osteoarthritis of ≥3 months * Patients with grade II and III OA of the Kellgren and Lawrence system for classification of osteoarthritis . * At least one active trigger point in GM * If both knees were diagnosed as OA, the most affected one was selected. * Current pain intensity on the Visual Analogue Scale (VAS) ≥4/10. * Subjects have sufficient cognition that enables them to understand the requirements of the study, comply with the study procedures, and visit schedule. * Diagnostic Criteria of KOA A diagnosis of knee osteoarthritis was made when knee pain is present, plus Osteophytes on radiographs, plus at least 1 of the following 3: * Age \> 50 years * Morning stiffness \< 30 minutes * Crepitus on active motion Exclusion Criteria: * Patients with any previous knee surgeries or lower limb fractures. * Chronic inflammatory diseases such as rheumatoid arthritis. * Signs of moderately significant knee synovitis include a warm and swollen (red) knee * History and/or physical examination findings compatible with knee internal derangement (e.g, positive Thessaly test). * Pregnancy * Patients who had undergone arthroscopy or treatment with intra-articular hyaluronic acid during the previous 6 months . * Use of NSAIDs one week before the screening visit . * Orthopedic diseases, or congenital musculoskeletal deformities, or neurological disorders that may affect or interfere with the therapeutic effect. * Participated in other intervention studies (strength training program or physiotherapy treatment for knee osteoarthritis) in the current period and the past 6 months . * Habitual use of psychotropic or narcotic analgesics for ≥1 week within 8 weeks prior to screening .
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Faculty of Physical Therapy, Cairo University
RECRUITINGGiza, Giza Governorate, 12613, Egypt
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