- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07736209
Effects of Heavy Back-Squat PAPE on Jump and Repeated Sprint Performance in Trained Soccer Players
29 de julio de 2026 actualizado por: Abdullah Demirli, Istanbul University - Cerrahpasa
The PAPE Paradox During Prolonged Repeated Sprint Performance: Acute Heavy Back-Squat Potentiates Vertical Jump and Early Sprint Performance But Impairs Overall Output-A Randomized Crossover Trial in Trained Soccer Players
This study examined whether performing heavy back squats before exercise affects jumping ability and repeated sprint performance in trained soccer players.
Twenty male university soccer players completed two testing sessions in a randomized crossover design.
In one session, participants performed a standardized warm-up only.
In the other session, they performed the same warm-up followed by three sets of three back-squat repetitions at 90% of their one-repetition maximum.
The two sessions were separated by one week.
After each condition, participants completed a countermovement jump test and an 18 × 40-meter repeated sprint test.
The study aimed to determine whether the heavy back-squat activity improves early explosive performance and whether it increases fatigue during prolonged repeated sprint exercise.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
20
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
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Istanbul
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Istanbul, Istanbul, Turquía (Türkiye), 34320
- İstanbul University Cerrahpaşa
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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
Descripción
Inclusion Criteria:
- Male soccer players aged 20-23 years.
- Currently competing in the top division of a university soccer league.
- A minimum of three years of regular soccer training experience.
- Free from long-term musculoskeletal injury during the previous six months.
- Willing and able to complete all familiarization, strength-testing, and experimental sessions.
- Provision of written informed consent.
Exclusion Criteria:
- A musculoskeletal injury resulting in an absence from training or competition for 21 days or longer during the previous six months.
- Use of medications or nutritional or ergogenic supplements that could affect exercise performance.
- Any health or physical condition preventing safe participation in heavy back-squat, countermovement jump, or repeated sprint testing.
- Failure to complete both experimental conditions.
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: Ciencia básica
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Control-PAPE Sequence
Participants first completed the Control condition, consisting of a standardized warm-up without an additional conditioning activity.
After a one-week washout period, participants completed the PAPE condition, consisting of the same standardized warm-up followed by three sets of three back-squat repetitions at 90% of one-repetition maximum, with 3 minutes of passive recovery between sets.
Countermovement jump and repeated sprint performance were assessed after each condition.
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Participants completed a standardized warm-up followed by a heavy back-squat conditioning activity consisting of three sets of three repetitions at 90% of one-repetition maximum.
Three minutes of passive recovery were provided between sets.
Countermovement jump performance was assessed approximately 4.5-5 minutes after the final squat set, immediately before the repeated sprint test.
Participants completed a standardized warm-up consisting of 5 minutes of jogging, followed by 10 bodyweight squats, 10 lunges, and 10 lateral shuffles.
No additional conditioning activity was performed.
After approximately 5 minutes of passive recovery, countermovement jump performance was assessed immediately before the repeated sprint test.
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Experimental: PAPE-Control Sequence
Participants first completed the PAPE condition, consisting of a standardized warm-up followed by three sets of three back-squat repetitions at 90% of one-repetition maximum, with 3 minutes of passive recovery between sets.
After a one-week washout period, participants completed the Control condition, consisting of the same standardized warm-up without an additional conditioning activity.
Countermovement jump and repeated sprint performance were assessed after each condition.
|
Participants completed a standardized warm-up followed by a heavy back-squat conditioning activity consisting of three sets of three repetitions at 90% of one-repetition maximum.
Three minutes of passive recovery were provided between sets.
Countermovement jump performance was assessed approximately 4.5-5 minutes after the final squat set, immediately before the repeated sprint test.
Participants completed a standardized warm-up consisting of 5 minutes of jogging, followed by 10 bodyweight squats, 10 lunges, and 10 lateral shuffles.
No additional conditioning activity was performed.
After approximately 5 minutes of passive recovery, countermovement jump performance was assessed immediately before the repeated sprint test.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Repeated Sprint Performance Decrement
Periodo de tiempo: During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Percentage decline in repeated sprint performance calculated from sprint times recorded during an 18 × 40-meter shuttle sprint test.
The protocol consisted of three sets of six 40-meter shuttle sprints, with 20 seconds of passive recovery between sprints and 4 minutes of passive recovery between sets.
Lower percentage values indicate better maintenance of sprint performance and less fatigue.
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During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Countermovement Jump Height
Periodo de tiempo: At approximately 5 minutes after the assigned condition, within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Maximum countermovement jump height measured in centimeters using the Optojump Next optical measurement system.
Participants performed three maximal countermovement jump trials with their hands positioned on their hips and 60 seconds of passive recovery between trials.
The highest jump height was used for analysis.
Higher values indicate better jump performance.
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At approximately 5 minutes after the assigned condition, within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Mean Repeated Sprint Time
Periodo de tiempo: During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Mean sprint time, measured in seconds, calculated across all 18 repetitions of the 40-meter shuttle sprint test.
Sprint times were recorded using a photocell timing system.
Lower values indicate better repeated sprint performance.
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During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Best Sprint Time
Periodo de tiempo: During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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The fastest sprint time, measured in seconds, recorded among the 18 repetitions of the 40-meter shuttle sprint test using a photocell timing system.
Lower values indicate better sprint performance.
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During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Worst Sprint Time
Periodo de tiempo: During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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The slowest sprint time, measured in seconds, recorded among the 18 repetitions of the 40-meter shuttle sprint test using a photocell timing system.
Lower values indicate better sprint performance.
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During the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period.
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Sprint Time Across Individual Repetitions
Periodo de tiempo: During each repetition of the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period
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Sprint time, measured in seconds, for each of the 18 individual 40-meter shuttle sprint repetitions.
Sprint-by-sprint values were used to evaluate changes in performance during the early repetitions (sprints 1-3), middle repetitions (sprints 4-8), and later repetitions (sprints 9-18).
Lower values indicate faster sprint performance.
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During each repetition of the 18 × 40-meter repeated sprint test, which lasted approximately 15 minutes and was completed within each of two experimental sessions lasting approximately 25-35 minutes; the sessions were separated by a 1-week washout period
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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)
20 de diciembre de 2025
Finalización primaria (Actual)
15 de febrero de 2026
Finalización del estudio (Actual)
15 de febrero de 2026
Fechas de registro del estudio
Enviado por primera vez
26 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
29 de julio de 2026
Publicado por primera vez (Actual)
30 de julio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
30 de julio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
29 de julio de 2026
Última verificación
1 de julio de 2026
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- PAPE-RSA-2025-01
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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