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Effects of ShoulderSphere Exercises in Young Adults

4 de junio de 2026 actualizado 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.

Descripción general del estudio

Descripción detallada

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 estudio

Intervencionista

Inscripción (Actual)

34

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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 activo: 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.
Otros nombres:
  • Thrower's Ten-Based Exercises

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in shoulder stability from baseline to 8 weeks
Periodo de tiempo: 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 resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in functional upper-extremity performance from baseline to 8 weeks
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

12 de mayo de 2024

Finalización primaria (Actual)

25 de julio de 2024

Finalización del estudio (Actual)

25 de julio de 2024

Fechas de registro del estudio

Enviado por primera vez

4 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 de junio de 2026

Publicado por primera vez (Actual)

11 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

11 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

4 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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