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Comparison of Balance, Core Stabilization Performance, Foot Reaction Time and Body Awareness in Young Amateur Football Players From Different Age Groups

27 de julio de 2026 actualizado por: Ezgi Türkmen, Health Institutes of Turkey
Aim of the study is to compare balance, core stabilization performance, foot reaction time, and body awareness in 50 amateur football players aged 13-19 (Group I: 13-15 years, and Group II: 16-19 years) according to age, and to determine age-related performance differences.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

The aim of this study is to evaluate balance, core stabilization performance, foot reaction time and body awareness in amateur football players aged 13-19 years, to examine how these parameters change according to age groups, and to compare and reveal developmental differences in these performance components in young athletes. This research study is designed as an observational and cross-sectional evaluation study. The study aims to collect and compare the data according to age on participants' sociodemographic data, balance status using the Y-Balance Test, endurance levels using the McGill Core Endurance Test, reaction time using the Nelson Foot Reaction Test, and awareness levels using the Body Awareness Questionnaire.

Tipo de estudio

De observación

Inscripción (Estimado)

50

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

  • Nombre: Ezgi Türkmen
  • Número de teléfono: 0090 216 547 26 00
  • Correo electrónico: turkmnezgi@gmail.com

Ubicaciones de estudio

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

  • Niño
  • Adulto

Acepta Voluntarios Saludables

Sí

Método de muestreo

Muestra no probabilística

Población de estudio

Amateur Football Players Aged 13-19

Descripción

Inclusion Criteria:

  • Being a licensed amateur football player aged 13-19.
  • Having played football regularly (at least 3 days a week) for the past year.
  • Voluntarily agreeing to participate in the study.

Exclusion Criteria:

  • Having a diagnosis of any neurological, orthopedic, or systemic disorder.
  • Having a diagnosis of visual impairment or any systemic disease affecting balance.
  • Having any significant physical limitations that would prevent the administration of the tests.
  • Having a diagnosed psychological disorder that would hinder communication.

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

Cohortes e Intervenciones

Grupo / Cohorte
Group I
Amateur Football Players Aged 13-15
Group II
Amateur Football Players Aged 16-19

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Nelson Foot Reaction Test
Periodo de tiempo: Baseline
The Nelson Foot Reaction Test measures simple foot-eye reaction time and lower limb neuromuscular coordination. Using a drop ruler, it requires the subject to quickly stop or "trap" a falling measurement stick between their foot and a wall or the floor in response to an auditory or visual trigger. The Reaction: The subject reacts as quickly as possible, pressing their foot forward to pinch/stop the falling ruler against the wall.Recording: The point where the ruler is stopped indicates the distance it traveled. The reaction time is calculated using the formula: Reaction Time (seconds) = √2 * Distance (cm)/980.
Baseline
Body Awareness Questionnaire (BAQ)
Periodo de tiempo: Baseline
BAQ is an 18-item self-report scale designed to measure how attentive you are to normal, non-emotional internal bodily processes. It evaluates your sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions. Typically takes about 3 to 5 minutes. Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived confidence and accuracy in monitoring your physical state over time.
Baseline
Y Balance Test (YBT)
Periodo de tiempo: Baseline
The YBT requires the athlete to balance on one leg whilst simultaneously reaching as far as possible with the other leg in three separate directions: anterior, posterolateral, and posteromedial. Therefore, this test measures the athlete's strength, stability and balance in various directions. The YBT composite score is calculated by summing the three reach directions and normalising the results to the lower limb length.
Baseline
McGill Core Endurance Test
Periodo de tiempo: Baseline
This test measures the stabilization capacity and muscle endurance of the core muscles (abdominal, back, oblique, and lower back muscles). It is performed in four positions: Trunk Flexor Test, Trunk Extensor Test (Sorensen Test), Side Bridge Test (Left & Right). The time (in seconds) spent maintaining the required positions is measured and recorded using a stopwatch.
Baseline

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Body Awareness Questionnaire (BAQ)
Periodo de tiempo: Baseline
BAQ is an 18-item self-report scale designed to measure how attentive you are to normal, non-emotional internal bodily processes. It evaluates your sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions. Typically takes about 3 to 5 minutes. Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived confidence and accuracy in monitoring your physical state over time.
Baseline
Y Balance Test (YBT)
Periodo de tiempo: Baseline
The YBT requires the athlete to balance on one leg whilst simultaneously reaching as far as possible with the other leg in three separate directions: anterior, posterolateral, and posteromedial. Therefore, this test measures the athlete's strength, stability and balance in various directions. The YBT composite score is calculated by summing the three reach directions and normalising the results to the lower limb length.
Baseline
McGill Core Endurance Test
Periodo de tiempo: Baseline
This test measures the stabilization capacity and muscle endurance of the core muscles (abdominal, back, oblique, and lower back muscles). It is performed in four positions: Trunk Flexor Test, Trunk Extensor Test (Sorensen Test), Side Bridge Test (Left & Right). The time (in seconds) spent maintaining the required positions is measured and recorded using a stopwatch.
Baseline

Colaboradores e Investigadores

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

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)

27 de julio de 2026

Finalización primaria (Estimado)

1 de agosto de 2026

Finalización del estudio (Estimado)

1 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

17 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

22 de julio de 2026

Publicado por primera vez (Actual)

24 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

28 de julio de 2026

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

27 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • ETurkmen0126

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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