Game-Based Versus Linear Sprint Training in Male Soccer Players (GBS-LST)
28 de agosto de 2026 actualizado por: Görkem Açar, Istanbul Gelisim University
A 12-Week Randomized Controlled Trial Evaluating the Time-Course Effects of Once-Weekly Game-Based Versus Linear Sprint Training on Soccer Performance and Hamstring Strength in Amateur Players During the Competitive Season
This randomized controlled trial investigated the effects of two different sprint training approaches on physical performance in male amateur soccer players during the competitive season. The study aimed to determine whether once-weekly game-based sprint training or linear sprint training could improve sprint performance, change-of-direction ability, hamstring strength, and maximum running velocity achieved during official matches.
Thirty-six male amateur soccer players were randomly assigned in a 1:1:1 ratio to one of three groups: the Game-Based Sprint Group, the Linear Sprint Group, or the Control Group. Participants in both sprint training groups completed one additional sprint training session per week for 12 weeks while continuing their regular soccer training and competition schedule. The Linear Sprint Group performed maximal 40-meter linear sprints, whereas the Game-Based Sprint Group performed soccer-specific sprint activities that included running, ball involvement, and technical actions. The Control Group continued regular soccer training without an additional sprint-specific intervention.
Sprint performance, change-of-direction performance, and right and left hamstring strength were assessed at baseline, Week 6, and Week 12. Maximum running velocity was also monitored during official matches throughout the 12-week study period. The study was designed to compare how the two sprint training approaches affected performance over time and whether changes observed during standardized testing were also reflected in maximum running velocity during competitive matches.
Descripción general del estudio
Estado
Estado
Terminado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Intervencionista
Inscripción (Actual)
Inscripción
36
Fase
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), 34310
- Istanbul Gelisim University
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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
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Sí
Descripción
Inclusion Criteria:
- Male amateur-licensed soccer players.
- A minimum of 5 years of regular soccer training experience.
- Participation in organized soccer training at least 5 days per week.
Exclusion Criteria:
- A serious musculoskeletal injury within the previous 6 months that could interfere with participation in the training intervention or performance assessments.
- Musculoskeletal surgery within the previous 6 months that could interfere with the study outcomes.
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: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
3
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
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Experimental: Linear Sprint Group (LSG)
Participants performed maximal 40-m linear sprint training once weekly on M-3 (Wednesday), approximately 72 hours before the official match, in addition to their regular soccer training.
The 12-week intervention was progressively structured across three four-week phases.
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Participants performed maximal 40-m linear sprints once weekly for 12 weeks.
During Weeks 1-4, participants completed 2 sets of 4 repetitions with 90 seconds of recovery between repetitions and 3 minutes between sets.
During Weeks 5-8, they completed 3 sets of 4 repetitions with the same recovery periods.
During Weeks 9-12, they completed 3 sets of 5 repetitions with 90 seconds of recovery between repetitions and 4 minutes between sets.
The intervention was performed in addition to regular soccer training.
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Experimental: Game-Based Sprint Group (GBSG)
Participants performed game-based sprint training once weekly on M-3 (Wednesday), approximately 72 hours before the official match, in addition to their regular soccer training.
Training consisted of soccer-specific maximal sprint actions within a standardized crossing-and-shooting drill incorporating ball involvement, perceptual demands, and technical actions.
The 12-week intervention was progressively structured across three four-week phases.
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Participants performed soccer-specific maximal sprint actions within a standardized crossing-and-shooting drill once weekly for 12 weeks.
During Weeks 1-4, participants completed 2 sets of 4 repetitions of 8-10-second contextual sprint actions, with 90 seconds of recovery between repetitions and 3 minutes between sets.
During Weeks 5-8, they completed 3 sets of 4 repetitions using the same sprint duration and recovery periods.
During Weeks 9-12, they completed 3 sets of 5 repetitions of 10-12-second contextual sprint actions, with 90 seconds of recovery between repetitions and 4 minutes between sets.
The drills incorporated ball involvement, perceptual demands, and soccer-specific technical actions.
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Sin intervención: Control Group (CG)
Participants continued their regular competitive-season soccer training and match schedule throughout the 12-week study period without receiving any additional sprint-specific intervention.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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40-m Sprint Performance
Periodo de tiempo: Baseline (Week 0), Week 6, and Week 12
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The time required to complete a 40-m maximal linear sprint was measured using the SmartSpeed electronic timing system (VALD Performance, Australia).
Participants completed two maximal trials, and the fastest time was retained for analysis.
Lower values indicate better sprint performance.
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Baseline (Week 0), Week 6, and Week 12
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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T-Drill Change-of-Direction Performance
Periodo de tiempo: Baseline (Week 0), Week 6, and Week 12
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Change-of-direction performance was assessed using the T-drill test.
Participants completed two maximal trials, and the fastest completion time was retained for analysis.
Lower values indicate better performance.
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Baseline (Week 0), Week 6, and Week 12
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Hamstring Strength
Periodo de tiempo: Baseline (Week 0), Week 6, and Week 12
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Bilateral hamstring strength was assessed using the NordBord system (VALD Performance).
Right and left limbs were assessed separately, with force recorded in Newtons (N).
Participants completed two maximal-effort trials for each limb, and the highest value was retained for analysis.
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Baseline (Week 0), Week 6, and Week 12
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Match Maximum Running Velocity
Periodo de tiempo: During official matches throughout the 12-week intervention period
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Maximum running velocity during official soccer matches was monitored using the Catapult S7 GPS system.
The highest running velocity achieved by each participant during each official match was retained for analysis.
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During official matches throughout the 12-week intervention period
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
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)
Inicio del estudio
1 de noviembre de 2025
Finalización primaria (Actual)
Finalización primaria
24 de enero de 2026
Finalización del estudio (Actual)
Finalización del estudio
24 de enero de 2026
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
28 de agosto de 2026
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
28 de agosto de 2026
Publicado por primera vez (Actual)
Publicado por primera vez
2 de septiembre de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
2 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
28 de agosto de 2026
Última verificación
Última verificación
1 de agosto de 2026
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
Otros números de identificación del estudio
- SPRINT-RCT-2025-397267
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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