Can a simple massage tool ease stubborn shoulder pain?
NCT ID NCT07293702
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether using a hand-held tool to massage the shoulder muscles (called IASTM) can reduce pain and improve movement in people with shoulder impingement. About 38 adults aged 40-60 with this condition will receive either standard exercise or exercise plus the massage tool over four weeks. The goal is to see if adding the tool helps more than exercise alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Instrument-assisted soft tissue mobilization (IASTM)
- What this could lead to
- If it works, this could offer a non-drug way to reduce shoulder pain and improve function for people with subacromial impingement syndrome.
- What could go wrong
- This is a small, early-stage trial with only 38 participants, so results may not apply to everyone. The added benefit of IASTM over exercise alone may be small or absent.
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 38 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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May 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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40 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Individuals diagnosed with SIS by MRI * Men and women between 40 and 60 years of age * Individuals with symptoms persisting for at least one month * Individuals with a minimum of 60° of shoulder flexion and abduction range of motion Exclusion Criteria: * Individuals with a history of surgery on the affected arm * Individuals with an open wound on the arm * Individuals with an active infection * Individuals with inflammatory joint disease * Individuals with malignant or benign tumors were excluded from the study.
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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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Istanbul Medipol University
RECRUITINGIstanbul, 34820, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can targeted mobilization ease shoulder impingement?
- Ultrasound-Guided injections may offer superior pain relief for common arm conditions
- Which shoulder therapy works best? mulligan vs PNF put to the test
- Shock wave plus pain gel: a new hope for sore shoulders?
- Neck moves might boost shoulder recovery, small trial hopes
- Progress reports may speed shoulder recovery