- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07642310
Effects of ShoulderSphere Exercises in Young Adults
Effects of ShoulderSphere Exercises on Shoulder Stabilization, Strength, Proprioception, and Endurance in Young Adults
This study evaluated the effects of ShoulderSphere exercises on shoulder stability, muscle strength, proprioception, endurance, and functional performance in young adults.
ShoulderSphere is an exercise device that provides dynamic and multi-directional resistance during shoulder movements. The study compared an 8-week ShoulderSphere-based exercise program with a conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
Young adults without current shoulder symptoms were included in the study. Participants were assigned to one of two exercise groups. Shoulder stability, functional upper-extremity performance, shoulder proprioception, and isokinetic muscle strength and endurance were assessed before and after the 8-week intervention.
The aim of the study was to determine whether ShoulderSphere exercises produced different effects compared with conventional shoulder stabilization exercises in young adults.
Przegląd badań
Status
Szczegółowy opis
This study was designed as a controlled pretest-posttest intervention study in young adults. The purpose was to compare the effects of an 8-week ShoulderSphere-based exercise program with a conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
Participants were young adults between 18 and 40 years of age who did not have current shoulder pain or clinical shoulder symptoms. Participants were assigned to either the ShoulderSphere exercise group or the conventional exercise group.
The ShoulderSphere group performed exercises using the ShoulderSphere device, which provides dynamic resistance and requires continuous control of shoulder movement. The conventional exercise group performed selected shoulder stabilization exercises based on the Thrower's Ten program. Both interventions were applied for 8 weeks.
Outcome assessments were performed before and after the intervention period. Shoulder stability was assessed using the Closed Kinetic Chain Upper Extremity Stability Test. Functional upper-extremity performance was assessed using the seated single-arm medicine ball throw test. Shoulder proprioception was assessed using an active joint position sense test. Isokinetic shoulder muscle strength and endurance were assessed using an isokinetic dynamometer.
The main purpose of the study was to examine whether ShoulderSphere exercises had different effects from conventional shoulder stabilization exercises on shoulder stability, strength, proprioception, endurance, and functional performance in young adults.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Ankara, Turcja (Türkiye), 06540
- Gazi University Graduate School of Health Sciences
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- Being between 18 and 40 years of age
- Having no current shoulder pain or clinical shoulder symptoms
- Meeting the study screening criterion for shoulder stability based on the Closed Kinetic Chain Upper Extremity Stability Test
- Volunteering to participate in the study
- Providing written informed consent
Exclusion Criteria:
- Having current shoulder pain or any clinical shoulder symptoms
- Having a history of shoulder surgery
- Having a history of shoulder dislocation, subluxation, or significant shoulder trauma
- Having any neurological, rheumatological, or systemic condition that could affect upper-extremity function
- Having an acute musculoskeletal injury affecting the shoulder, neck, back, or upper extremity
- Having any condition that would prevent safe participation in the exercise program or outcome assessments
- Unable to complete the intervention or assessment procedures
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Inny
- Przydział: Nielosowe
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: ShoulderSphere Exercise Group
Participants in this arm performed an 8-week ShoulderSphere-based shoulder exercise program.
The exercises were performed using the ShoulderSphere device and aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance.
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Participants performed an 8-week shoulder exercise program using the ShoulderSphere device.
The program aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance through dynamic and multi-directional shoulder control exercises.
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Aktywny komparator: Conventional Shoulder Stabilization Exercise Group
Participants in this arm performed an 8-week conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
The exercises aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance.
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Participants performed an 8-week conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
The program aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance.
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in shoulder stability from baseline to 8 weeks
Ramy czasowe: Baseline and 8 weeks
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Shoulder stability was assessed using the Closed Kinetic Chain Upper Extremity Stability Test.
The number of touches completed during the test was recorded before and after the 8-week intervention period.
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Baseline and 8 weeks
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in functional upper-extremity performance from baseline to 8 weeks
Ramy czasowe: Baseline and 8 weeks
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Functional upper-extremity performance was assessed using the seated single-arm medicine ball throw test.
The throwing distance was recorded before and after the 8-week intervention period.
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Baseline and 8 weeks
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Change in shoulder proprioception from baseline to 8 weeks
Ramy czasowe: Baseline and 8 weeks
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Shoulder proprioception was assessed using an active joint position sense test for internal and external rotation.
Absolute error values were recorded before and after the 8-week intervention period.
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Baseline and 8 weeks
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Change in isokinetic shoulder muscle strength from baseline to 8 weeks
Ramy czasowe: Baseline and 8 weeks
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Isokinetic shoulder muscle strength was assessed using an isokinetic dynamometer during internal and external rotation.
Measurements were performed before and after the 8-week intervention period.
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Baseline and 8 weeks
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Change in isokinetic shoulder muscle endurance from baseline to 8 weeks
Ramy czasowe: Baseline and 8 weeks
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Isokinetic shoulder muscle endurance was assessed using an isokinetic dynamometer during repeated shoulder internal and external rotation movements.
Measurements were performed before and after the 8-week intervention period.
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Baseline and 8 weeks
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Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Inne numery identyfikacyjne badania
- GAZI-2022-933-SS
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
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