Exercise eases shoulder fatigue in new study
NCT ID NCT05443295
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a supervised exercise program (MoveUS) could reduce fatigue and improve quality of life in 108 adults with shoulder instability. Participants were randomly assigned to either the exercise program or usual care. The results will help determine if this approach can reduce shoulder dislocations and fatigue, and be used in clinics.
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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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108 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Mar 2025
- 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 64 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: * Having suffered at least one episode of glenohumeral instability in the last year. * Age between 18 and 64 years. * Have signed the informed consent. * Score equal to or less than 6 on the Instability Severity Index Score. Exclusion Criteria: * Ethical or cultural barriers. * Lack of command of Spanish language. * Underlying diseases or concomitant treatments that may affect exercise capacity. * Participation in other clinical trials. * Score equal to or greater than 1800 on the Western Ontario Shoulder Instability Index.
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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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Antonio Cuesta Vargas
Málaga, Málaga, Spain
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Hospital Comarcal de la Axarquía
Málaga, Spain
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Other studies related to the condition(s) this trial covers.
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