Workout your good arm to save the bad one? new study tests the idea
NCT ID NCT06905093
First seen Jun 24, 2026 · Last updated Jul 08, 2026 · Updated 3 times
Summary
This study looks at whether training the arm that isn't in a sling can help preserve muscle strength and size in the immobilized arm after shoulder surgery. 42 adults undergoing shoulder surgery will be split into three groups: standard rehab, eccentric training, or concentric training of the non-immobilized arm. The goal is to see if this approach can lead to faster and better recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- exercise (eccentric or concentric training of the non-immobilized arm)
- What this could lead to
- If successful, this could lead to better rehabilitation strategies that reduce muscle loss and speed recovery after shoulder surgery with immobilization.
- What could go wrong
- This is a small, early-stage study with only 42 participants, so results may not apply to all patients. The benefits of contralateral training are still unproven, and individual responses may vary.
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 42 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Oct 2027
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 years and older
- 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: * Adult patient (≥ 18 years old) undergoing shoulder surgery (i.e., Bankart procedure, rotator cuff repair, arthroplasty) * With an indication for immobilization, expected to last 4 to 6 weeks * Free from any neurological pathology * Having provided their informed consent before any participation in the research Exclusion Criteria: * Having a medical contraindication to the practice of physical and sports activities * Presenting an expected modification of their physical activity of the non-immobilized limb * Having suffered an injury to the upper limbs in the last 6 months * Having already undergone surgery on the upper limbs * Pregnant, parturient, and breastfeeding women * Presenting a medically established alteration of their cognitive functions * Subject under guardianship, curatorship, family empowerment, or judicial safeguard * Not affiliated or beneficiary of health insurance coverage * Any other reason that, in the investigator's opinion, could interfere with the evaluation of the study objectives
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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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Hôpital National d'Instruction des Armées Sainte-Anne
RECRUITINGToulon, Var, 83000, France
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