- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07726459
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
Condiciones
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
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Istanbul, Turquía (Türkiye)
- Reclutamiento
- Haliç Üniversitesi
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Contacto:
- Ayşenur Çetinkaya, PhD
- Número de teléfono: 0090 212 924 24 44
- Correo electrónico: aysenurcetinkaya@halic.edu.tr
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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 |
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Group I
Amateur Football Players Aged 13-15
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Group II
Amateur Football Players Aged 16-19
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Nelson Foot Reaction Test
Periodo de tiempo: Baseline
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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.
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Baseline
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Body Awareness Questionnaire (BAQ)
Periodo de tiempo: Baseline
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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.
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Baseline
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Y Balance Test (YBT)
Periodo de tiempo: Baseline
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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.
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Baseline
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McGill Core Endurance Test
Periodo de tiempo: Baseline
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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.
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Baseline
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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.
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Baseline
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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
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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)
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
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