Shock wave combo may ease stubborn shoulder pain
NCT ID NCT07390396
First seen Jun 26, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This study tests whether adding shock wave therapy to a standard exercise program can reduce pain and improve shoulder function in people with rotator cuff tendinopathy. Fifty adults aged 30 to 55 with chronic shoulder pain will receive either exercises alone or exercises plus shock waves once a week for six weeks. The goal is to see if the combination leads to better tendon healing and strength.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Extracorporeal shock wave therapy (ESWT) plus exercise
- What this could lead to
- If it works, this could offer a better way to treat chronic shoulder pain without surgery, combining shock waves with standard exercises.
- What could go wrong
- This is a small, early-stage trial with only 50 participants. The results may not apply to everyone, and shock wave therapy can cause temporary pain or bruising.
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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50 people
The number who actually took part.
- Started
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Dec 2025
- Finished
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May 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.
- Ages
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30 to 55 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.
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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: * Medically stable individuals who consent to participate in the study. * Male and female participants aged between 30 and 55 years. * Diagnosed with rotator cuff tendinopathy, confirmed clinically and by ultrasound or MRI. * Duration of symptoms greater than 3 months. * Supraspinatus tendon thickness \> 5.85 mm as measured by ultrasound (based on Hunter et al., 2021). * Able to follow the treatment plan and attend all therapy sessions. Exclusion Criteria: * Massive rotator cuff tear or complete tendon rupture. * Adhesive capsulitis or significant limitation of passive shoulder motion. * History of shoulder fracture, dislocation, or surgery in the affected limb. * Rheumatoid arthritis, diabetes mellitus, or systemic inflammatory disease. * Cervical radiculopathy or neurological involvement affecting the shoulder. * Corticosteroid injection in the affected shoulder within the last 6 months. * Pregnancy or breastfeeding. * BMI \> 30 kg/m² (obese individuals excluded). * Current malignancy, open wounds, or local infection at the treatment site. * Inability to tolerate shock wave therapy or perform exercise sessions.
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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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faculty of physical therapy, Deraya University
Minya, Menia Governorate, Egypt
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