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Effects of ShoulderSphere Exercises in Young Adults

4 de junho de 2026 atualizado por: 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.

Visão geral do estudo

Descrição detalhada

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 de estudo

Intervencional

Inscrição (Real)

34

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Outro
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.
Comparador Ativo: 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.
Outros nomes:
  • Thrower's Ten-Based Exercises

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in shoulder stability from baseline to 8 weeks
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change in functional upper-extremity performance from baseline to 8 weeks
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

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Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

12 de maio de 2024

Conclusão Primária (Real)

25 de julho de 2024

Conclusão do estudo (Real)

25 de julho de 2024

Datas de inscrição no estudo

Enviado pela primeira vez

4 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

4 de junho de 2026

Primeira postagem (Real)

11 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

11 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

4 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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