Targeted eccentric exercise may rebuild shoulder function — a trial puts it to the test
NCT ID NCT07727941
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This trial investigates whether eccentric isokinetic exercise — a type of controlled, lengthening muscle contraction performed on a special machine — can reduce pain and improve shoulder function in people with rotator cuff tendinopathy. Fifty adults aged 20 to 50 with confirmed tendinopathy will either do this machine-based exercise plus a standard home program, or the home program alone. Researchers will measure changes in pain, shoulder function, and muscle structure using ultrasound.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- eccentric isokinetic exercise on a Humac Norm II device
- What this could lead to
- If effective, this could offer a targeted exercise approach to ease shoulder pain and improve function without surgery.
- What could go wrong
- This is a small, early-stage trial with only 50 participants, so results may not apply broadly. The exercise program requires special equipment, limiting accessibility.
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.
- Participants
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50 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Feb 2026
- 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.
Who is studied
Adult patients presenting to the Prof. Dr. Cemil Taşcıoğlu City Hospital Physical Therapy Outpatient Clinic with complaints of shoulder pain.
- Ages
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20 to 50 years
- Sex
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Anyone
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria:Being between the ages of 20 and 50 * Having a diagnosis of rotator cuff tendinopathy based on medical history, physical examination, and MRI findings * Having full shoulder joint range of motion * Absence of upper extremity deformity that would interfere with ultrasonographic measurement * Having provided written informed consent Exclusion Criteria:Glenohumeral instability * Adhesive capsulitis (stages 2-3) * Radiographic evidence of calcific tendinitis or significant bursitis •Cervical radiculopathy Upper extremity or spinal deformities * History of surgery involving the shoulder, cervical spine, or back * Neurological or systemic disease (rheumatological, metabolic, etc.) * Physical therapy for the shoulder, neck, or back region within the last 6 months * Corticosteroid injection into the affected shoulder within the last 6 months * Exposure to intensive repetitive shoulder movements in sports or occupational activities * Use of medications that could affect exercise performance or metabolic response
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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.
Contacts and locations
Locations
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Prof. Dr. Cemil Taşcıoğlu City Hospital
Istanbul, Turkey (Türkiye)
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Prof. Dr. Cemil Taşcıoğlu City Hospital
Istanbul, şişli, 34384, Turkey (Türkiye)
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