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Effects of a 12-week T10 Exercise Program on Shooting Performance, Upper Extremity Function, Balance and Reaction Time in Competitive Air Pistol Athletes (Air pistol T10)

26 de junio de 2026 actualizado por: Nazli Cigercioglu, Hacettepe University

The Effects of a 12-Week T10 Exercise Program on Shooting Performance, Upper Extremity Function, Balance, and Reaction Time in Air Pistol Athletes: A Randomized Controlled Trial

Air pistol shooting requires a high level of postural stability, upper extremity neuromuscular control, and concentration to achieve optimal performance. Prolonged maintenance of the shooting position may lead to shoulder muscle fatigue, reduced joint stability, and impaired shooting accuracy. Although sport-specific exercise programs have been recommended to improve physical performance in shooters, the effectiveness of the T10 exercise program has not yet been investigated in this population. This randomized controlled trial aims to evaluate the effects of a 12-week T10 exercise program, in addition to routine training, on shooting performance in competitive air pistol athletes. Secondary outcomes include upper and lower extremity functional performance, balance, muscular endurance, upper extremity stability, grip strength, medicine ball throw performance, and visual and auditory reaction time. Participants will be randomly allocated to either an intervention group receiving the T10 exercise program plus routine training or a control group continuing routine training alone. Assessments will be performed at baseline and after the 12-week intervention. The findings of this study may provide evidence for the effectiveness of a sport-specific neuromuscular exercise program in enhancing shooting performance and physical function in competitive air pistol athletes.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

Air pistol shooting is a precision sport that requires a high level of postural stability, upper extremity neuromuscular control, and sustained concentration to achieve accurate shooting performance. During competition, athletes maintain the shoulder in an elevated position for prolonged periods, which may result in muscle fatigue, impaired scapular stability, altered shoulder mechanics, and reduced shooting accuracy. In addition, deficiencies in balance, upper extremity stability, muscular endurance, and reaction time may negatively influence shooting performance.

Previous studies have suggested that physical conditioning and sport-specific exercise programs may improve athletic performance in shooting sports. The T10 exercise program is a comprehensive upper extremity training protocol consisting of ten exercises designed to improve neuromuscular control, dynamic stabilization, co-contraction, muscle strength, endurance, coordination, and movement quality. Despite its potential benefits, the effectiveness of the T10 exercise program has not been investigated in competitive air pistol athletes.

The primary objective of this randomized controlled trial is to determine the effects of a 12-week T10 exercise program on shooting performance in competitive air pistol athletes. Secondary objectives are to evaluate the effects of the intervention on upper extremity functional performance, upper extremity stability, dynamic balance, static balance, muscular endurance, grip strength, medicine ball throw performance, agility, lower extremity explosive performance, and visual and auditory reaction time.

A minimum of 24 competitive air pistol athletes aged 18 to 40 years will be recruited and randomly allocated to either an intervention group or a control group using simple randomization. Participants in the intervention group will perform the T10 exercise program three times per week for 12 weeks in addition to their routine shooting training, whereas participants in the control group will continue their routine training without additional exercises.

Outcome assessments will be performed at baseline and after the 12-week intervention. The primary outcome will be shooting performance. Secondary outcomes will include Upper Quarter Y Balance Test, Y Balance Test, Flamingo Balance Test, grip strength, medicine ball throw test, Closed Kinetic Chain Upper Extremity Stability Test, push-up and sit-up performance, T-test, standing long jump, and visual and auditory reaction time. The findings of this study are expected to provide evidence regarding the effectiveness of a sport-specific neuromuscular exercise program for improving shooting performance and physical function in competitive air pistol athletes and may contribute to the development of evidence-based training strategies for precision shooting sports.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

24

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.

Estudio Contacto

Ubicaciones de estudio

    • Kulu
      • Konya, Kulu, Turquía (Türkiye), 42950
        • Kulu Faculty of Health Science
        • Contacto:
          • Zilan Bazancir-Apaydin, Assoc. Prof.
          • Número de teléfono: +90 5078354961
          • Correo electrónico: bazancirzilan@gmail.com

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

Sí

Descripción

Inclusion Criteria:

  • Age between 18 and 40 years.
  • Competitive air pistol athletes with at least 2 years of regular shooting experience.
  • Participating in shooting training for at least 6 hours per week.
  • Being in the preseason training period.
  • Willing to participate and able to provide written informed consent.

Exclusion Criteria:

  • Current upper extremity musculoskeletal injury or pain.
  • History of upper extremity orthopedic surgery.
  • Neurological or cognitive disorders affecting participation.
  • Visual or hearing impairments that may interfere with testing or shooting performance.
  • Inflammatory joint disease involving the lower extremities.
  • History of lower extremity orthopedic surgery or musculoskeletal deformity affecting performance.
  • Rheumatologic, metabolic, or cardiovascular disease.
  • Body mass index (BMI) >30 kg/m².
  • Current use of psychiatric medication.
  • Failure to attend two consecutive intervention sessions during the study period.

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Intervention Group
Participants will receive the T10 exercise program three times per week for 12 weeks in addition to their routine shooting training.
Participants in the control group will continue their regular shooting training throughout the 12-week study period without receiving the T10 exercise program or any additional physiotherapist-supervised exercise intervention. Routine training will be conducted according to the athletes' usual training schedule under the supervision of their shooting coaches and will include technical shooting practice, aiming exercises, competition-specific drills, and standard warm-up activities. Participants will be instructed to maintain their usual training habits and refrain from initiating any additional upper extremity strengthening or neuromuscular exercise programs during the study period.
Experimental: Control Group
Participants will continue their routine shooting training without any additional exercise intervention.
Participants in the control group will continue their regular shooting training throughout the 12-week study period without receiving the T10 exercise program or any additional physiotherapist-supervised exercise intervention. Routine training will be conducted according to the athletes' usual training schedule under the supervision of their shooting coaches and will include technical shooting practice, aiming exercises, competition-specific drills, and standard warm-up activities. Participants will be instructed to maintain their usual training habits and refrain from initiating any additional upper extremity strengthening or neuromuscular exercise programs during the study period.
Otros nombres:
  • routine shooting training

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Shooting Performance Score
Periodo de tiempo: Baseline and 12 weeks
Shooting performance will be assessed according to the official International Shooting Sport Federation (ISSF) rules using the athletes' total shooting score obtained during a standardized air pistol shooting test. Higher scores indicate better shooting performance.
Baseline and 12 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
1. Upper Quarter Y Balance Test
Periodo de tiempo: Baseline and 12 weeks
Upper extremity dynamic balance and stability will be assessed using the Upper Quarter Y Balance Test. Reach distances in the medial, superolateral, and inferolateral directions will be recorded and normalized to upper limb length.
Baseline and 12 weeks
2. Y Balance Test
Periodo de tiempo: Baseline and 12 weeks
Dynamic balance of the lower extremity will be evaluated using the Y Balance Test. Reach distances in the anterior, posteromedial, and posterolateral directions will be recorded and normalized to leg length.
Baseline and 12 weeks
3. Flamingo Balance Test
Periodo de tiempo: Baseline and 12 weeks
Static balance performance will be assessed by recording the duration participants maintain balance on a narrow beam.
Baseline and 12 weeks
4. Grip Strength
Periodo de tiempo: Baseline and 12 weeks
Maximal isometric handgrip strength will be measured using a Jamar hand dynamometer. The mean of three trials will be recorded in kilograms (kg).
Baseline and 12 weeks
5. Medicine Ball Throw Test
Periodo de tiempo: Baseline and 12 weeks
Upper extremity explosive performance will be evaluated using a 3-kg medicine ball throw. Throwing distance will be recorded in centimeters (cm).
Baseline and 12 weeks
6. Closed Kinetic Chain Upper Extremity Stability Test (CKCUEST)
Periodo de tiempo: Baseline and 12 weeks
Upper extremity stability and functional performance will be assessed using the number of touches completed within 15 seconds.
Baseline and 12 weeks
7. Push-up Test
Periodo de tiempo: Baseline and 12 weeks
Upper extremity muscular endurance will be assessed by recording the maximum number of push-ups completed within one minute.
Baseline and 12 weeks
8. Sit-up Test
Periodo de tiempo: Baseline and 12 weeks
Core muscular endurance will be assessed by recording the maximum number of sit-ups completed within one minute.
Baseline and 12 weeks
9. T-Test
Periodo de tiempo: Baseline and 12 weeks
Agility performance will be assessed using the T-Test, with completion time recorded in seconds. Lower values indicate better agility performance.
Baseline and 12 weeks
10. Standing Long Jump Test
Periodo de tiempo: Baseline and 12 weeks
Lower extremity explosive power will be evaluated by measuring jump distance in centimeters (cm).
Baseline and 12 weeks
11. Visual Reaction Time
Periodo de tiempo: Baseline and 12 weeks
Visual reaction time will be measured using the Newtest 1000 reaction timer. The average response time will be recorded in milliseconds (ms).
Baseline and 12 weeks
12. Auditory Reaction TimeAuditory
Periodo de tiempo: Baseline and 12 weeks
reaction time will be measured using the Newtest 1000 reaction timer. The average response time will be recorded in milliseconds (ms).
Baseline and 12 weeks
13. Ruler Drop Test
Periodo de tiempo: Baseline and 12 weeks
Reaction time will also be assessed using the ruler drop test. The catching distance will be recorded in centimeters (cm).
Baseline and 12 weeks

Colaboradores e Investigadores

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

Patrocinador

Publicaciones y enlaces útiles

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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 (Estimado)

10 de julio de 2026

Finalización primaria (Estimado)

15 de noviembre de 2026

Finalización del estudio (Estimado)

15 de diciembre de 2027

Fechas de registro del estudio

Enviado por primera vez

26 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

26 de junio de 2026

Publicado por primera vez (Actual)

2 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de julio de 2026

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

26 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

Descripción del plan IPD

Individual participant data (IPD) will not be made publicly available because the study includes a small sample size of competitive athletes, which may increase the risk of participant identification despite de-identification. Only aggregate, anonymized study results will be reported in publications and presentations.

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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