- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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.
Panoramica dello studio
Stato
Descrizione dettagliata
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.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Ankara, Turchia (Türkiye), 06540
- Gazi University Graduate School of Health Sciences
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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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Comparatore attivo: 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.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in shoulder stability from baseline to 8 weeks
Lasso di tempo: 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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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in functional upper-extremity performance from baseline to 8 weeks
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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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Collaboratori e investigatori
Sponsor
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Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- GAZI-2022-933-SS
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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