Pre- and Post-Training Assessment of Sprint Performance, Agility, Balance and Body Awareness in Football Players Regarding Hamstring Injury
30 de julio de 2026 actualizado por: Ezgi Türkmen, Health Institutes of Turkey
Aim of the study is to examine the impact of a history of hamstring injury on athletes by determining and comparing the pre- and post-training levels of sprint performance, agility, dynamic balance, and body awareness in football players with and without a history of hamstring injury.
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Descripción detallada
The aim of this study is to compare sprint performance (10-meter sprint test (10mST) and 30-meter sprint test (30mST)), agility (T-Test of Agility), dynamic balance (Y-Balance Test), and body awareness (Body Awareness Questionnaire) levels in licensed football players with and without a history of hamstring injury, before and after training, in order to reveal the effect of a history of hamstring injury on functional performance and acute fatigue response.
Capturing acute changes with pre- and post-training measurements and comparing these between groups with and without a history of injury has the potential to make visible "intra-day/intra-training performance fluctuations" that may be overlooked upon returning to the field.
This research study is designed as an observational and cross-sectional evaluation study.
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
- 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
- Adulto
Acepta Voluntarios Saludables
Sí
Método de muestreo
Muestra no probabilística
Población de estudio
Licensed Football Players Aged 18-35 with and without a History of Hamstring Injury
Descripción
Inclusion Criteria:
- Being a licensed male football player aged 18-35.
- Having played football actively for at least 2 years.
- Having attended training sessions regularly within the last 6 months.
- Having a history of hamstring injury (n=25).
- Not having a history of hamstring injury (n=25).
- Voluntarily agreeing to participate in the study.
Exclusion Criteria:
- Having a current history of a diagnosed musculoskeletal injury in the lower extremities.
- Having undergone lower extremity surgery within the last 6 months.
- Having a diagnosis of any neurological, orthopedic, or systemic disorder.
- Having a diagnosis of any systemic disease affecting balance.
- Having any significant physical limitations that would prevent the application 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
Football players with a history of hamstring injury
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Group II
Football players without a history of hamstring injury
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Sprint Performance (10-meter and 30-meter Sprint Tests)
Periodo de tiempo: Before and immediately after training
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To evaluate the acceleration and maximum sprint performance of the football players, 10-meter and 30-meter sprint tests will be conducted.
The 10-meter sprint test will be used to assess acceleration and explosive power capacity over short distances.
Participants will stand in a semi-prone position behind the starting line and will begin a 10-meter run at maximum speed upon receiving the starting command.
The time will be recorded in seconds.
The 30-meter sprint test will be used to evaluate maximum running speed, sprint performance, and anaerobic capacity.
Similarly, participants will begin a 30-meter run at maximum speed upon receiving the starting command.
The time will be recorded in seconds.
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Before and immediately after training
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T-Test of Agility
Periodo de tiempo: Before and immediately after training
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This test will be administered to assess participants' agility, speed of change of direction, coordination, and reaction capacity.
The test course is arranged in a 'T' shape using cones, with 10 meters forward from the starting point and 5 meters to the right and left.
Participant runs forward from the starting point to the midpoint, then moves sideways to the right and left as quickly but steadily as possible, and finally runs back to the starting point.
The test duration is recorded in seconds using a stopwatch.
Shorter test times indicate a higher level of agility and neuromuscular control.
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Before and immediately after training
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Y Balance Test
Periodo de tiempo: Before and immediately after training
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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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Before and immediately after training
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Body Awareness Questionnaire (BAQ)
Periodo de tiempo: Before and immediately after training
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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 conKdence and accuracy in monitoring your physical state over time.
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Before and immediately after training
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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)
30 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
24 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
24 de julio de 2026
Publicado por primera vez (Actual)
30 de julio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
31 de julio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
30 de julio de 2026
Última verificación
1 de julio de 2026
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- ETurkmen0226
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. .