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Effects of ShoulderSphere Exercises in Young Adults

4 juin 2026 mis à jour par: Gökhan KARATAY, Gazi University

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.

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

34

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Ankara, Turquie (Türkiye), 06540
        • Gazi University Graduate School of Health Sciences

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

La description

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 d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.
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.
Comparateur actif: 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.
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.
Autres noms:
  • Thrower's Ten-Based Exercises

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in shoulder stability from baseline to 8 weeks
Délai: Baseline and 8 weeks
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.
Baseline and 8 weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in functional upper-extremity performance from baseline to 8 weeks
Délai: Baseline and 8 weeks
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.
Baseline and 8 weeks
Change in shoulder proprioception from baseline to 8 weeks
Délai: Baseline and 8 weeks
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.
Baseline and 8 weeks
Change in isokinetic shoulder muscle strength from baseline to 8 weeks
Délai: Baseline and 8 weeks
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.
Baseline and 8 weeks
Change in isokinetic shoulder muscle endurance from baseline to 8 weeks
Délai: Baseline and 8 weeks
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.
Baseline and 8 weeks

Collaborateurs et enquêteurs

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

12 mai 2024

Achèvement primaire (Réel)

25 juillet 2024

Achèvement de l'étude (Réel)

25 juillet 2024

Dates d'inscription aux études

Première soumission

4 juin 2026

Première soumission répondant aux critères de contrôle qualité

4 juin 2026

Première publication (Réel)

11 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

11 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

4 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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