Radiofrequency heat vs. exercise for aching shoulders
NCT ID NCT07823933
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers test whether TECAR therapy, a radiofrequency treatment that warms deep shoulder tissues, adds benefit to a standard exercise program for people with rotator cuff tendinopathy. Thirty-six participants receive either TECAR plus exercise or exercise alone. The trial measures changes in pain intensity and shoulder function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- TECAR therapy, a radiofrequency treatment that heats deep shoulder tissues
- What this could lead to
- If it works, TECAR therapy could offer a non-invasive option to ease shoulder pain and improve movement alongside standard exercise.
- What could go wrong
- This is a small study of 36 people, so results may not apply broadly. TECAR therapy is newer and its added benefit over exercise alone remains uncertain.
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 36 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 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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18 to 75 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: 1. Individuals experiencing pain in the shoulder and/or lateral deltoid region, with pain exacerbation during overhead activities. 2. Individuals exhibiting tenderness upon palpation at the rotator cuff tendon insertion site on the proximal humerus and/or restricted range of motion during active shoulder flexion, abduction, and internal and external rotation upon physical examination. 3. Individuals diagnosed with rotator cuff tendinosis or a partial-thickness tendon tear via imaging methods (ultrasound, magnetic resonance imaging). Exclusion Criteria: 1. Full-thickness rotator cuff tear 2. Previous shoulder surgery 3. Presence of other conditions capable of causing shoulder pain and loss of function (other joint pathologies, cervical radiculopathy, etc.) 4. Systemic diseases such as diabetes, rheumatoid arthritis, hepatitis, or coagulopathy 5. Pregnancy 6. Infection 7. Pacemaker 8. Peripheral circulatory disorder 9. Known concomitant malignancy or end-stage organ failure 10. Intra-articular/subacromial steroid injection within the last 6 weeks or NSAID treatment within the last week.
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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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Bilkent City Hospital
Ankara, Çankaya, Turkey (Türkiye)
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