- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07653425
Traditional Versus Cluster Resistance Training in Striking Combat Sport Athletes (TRG-CLG)
11 de junio de 2026 actualizado por: Amador García Ramos, Universidad de Granada
Effects of Traditional and Cluster Resistance Training Using Four Multi-Joint Exercises on Neuromuscular Performance in Striking Combat Sport Athletes
This randomized controlled trial compared the effects of traditional and cluster resistance training on neuromuscular performance in amateur striking combat sport athletes.
Twenty-eight athletes completed a 6-week full-body resistance training program including squat, bench press, deadlift, and bench pull exercises.
Participants were assigned to either a traditional training group, which performed repetitions continuously, or a cluster training group, which incorporated short intra-set rest periods.
Neuromuscular performance was assessed before and after the intervention through countermovement jump height, medicine-ball throw distance, and load-velocity relationship variables obtained from the four resistance exercises.
The study aimed to determine whether cluster resistance training provides superior neuromuscular adaptations compared with traditional resistance training when training volume and relative intensity are matched.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
32
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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-
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Concepción, Chile
- Universidad Católica de la Santísima Concepción
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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
Descripción
Inclusion Criteria:
- Healthy men and women aged 18 years or older. Active participation in striking combat sports (boxing, kickboxing, or karate) for at least 3 years.
- Minimum of 1 year of experience with the resistance exercises included in the study (squat, bench press, deadlift, and bench pull).
- Willingness to refrain from participating in additional strength training programs during the study period.
- Provision of written informed consent.
Exclusion Criteria:
- Presence of any musculoskeletal injury during the 6 months preceding data collection.
- Any medical condition that could contraindicate participation in resistance training.
- Failure to complete the training intervention or testing procedures.
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 paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: Traditional
Participants performed a 6-week full-body resistance training program consisting of squat, bench press, deadlift, and bench pull exercises.
Training was conducted twice per week and included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
Participants completed all repetitions consecutively within each set without intra-set rest periods.
Inter-set rest intervals were 3 minutes and inter-exercise rest intervals were 5 minutes.
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Participants completed a 6-week full-body resistance training program consisting of squat, bench press, deadlift, and bench pull exercises.
Training was performed twice weekly and included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
All repetitions within a set were performed consecutively without intra-set rest periods.
Participants were instructed to execute the concentric phase of each repetition with maximal intended velocity.
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Experimental: Cluster
Participants performed the same 6-week full-body resistance training program as the traditional training group, consisting of squat, bench press, deadlift, and bench pull exercises performed twice per week.
Training included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
The repetitions were organized into clusters of two repetitions separated by 15-second intra-set rest intervals (2 + 2 + 2 + 2 repetitions).
Inter-set rest intervals were 3 minutes and inter-exercise rest intervals were 5 minutes.
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Participants completed a 6-week full-body resistance training program consisting of squat, bench press, deadlift, and bench pull exercises.
Training was performed twice weekly and included 3 sets of 8 repetitions at 75% of the individual one-repetition maximum (1RM) for each exercise.
Repetitions were organized into clusters of two repetitions separated by 15-second intra-set rest intervals (2 + 2 + 2 + 2 repetitions).
Participants were instructed to execute the concentric phase of each repetition with maximal intended velocity.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Load-velocity relationship (LVR).
Periodo de tiempo: Baseline and after 6 weeks of resistance training
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Individual LVR were determined for the squat, bench press, and bench pull exercises using a Smith machine (FFittech, Taiwan, China), whereas the deadlift exercise was performed with a hexagonal barbell.
Each test started with an initial external load of 20 kg, which was progressively increased until the mean velocity (MV) of the fastest repetition differed by less than 0.30 m·s-1 from the theoretical MV associated with the 1RM of each exercise (0.30 m/s for squat, 0.15 m/s for deadlift, 0.17 m/s for bench press, and 0.50 m/s for bench pull) (Weakley et al., 2021).
The load increments were adjusted according to the exercise and movement velocity to ensure an appropriate distribution of loads across the individual force-velocity spectrum.
Three repetitions were performed at lighter loads, whereas only two repetitions were completed at heavier loads.
A standardized rest interval of 10 seconds was provided between repetitions at the same load.
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Baseline and after 6 weeks of resistance training
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Countermovement jump
Periodo de tiempo: Baseline and after 6 weeks of resistance training
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Participants completed three CMJ attempts with a 1-minute recovery period between trials.
From a standing position with feet approximately shoulder-width apart and hands placed on the hips, participants performed a rapid countermovement to a self-selected depth and immediately executed a maximal vertical jump.
Jump height was estimated from flight time using the equation: height = (flight time2 × 9.81 m·s-2) / 8, where 9.81 m·s-2 corresponds to gravitational acceleration.
Flight time was recorded using an infrared optical measurement system (OptoJump, Microgate, Bolzano, Italy).
Participants were instructed to maintain their hands on the hips during the entire movement and to land with the lower limbs fully extended.
Trials not complying with these technical requirements were discarded and repeated after 1 minute of rest under the supervision of the same experienced evaluator.
The best performance obtained across the three trials was retained for subsequent analyses.
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Baseline and after 6 weeks of resistance training
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Medicine ball throw (MBT).
Periodo de tiempo: Baseline and after 6 weeks of resistance training
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Upper-body explosive performance was evaluated using a seated MBT test performed with a 3-kg medicine ball.
Testing was conducted indoors on a hardwood surface.
Participants sat behind a marked line with both feet in contact with the floor and executed a single-arm forward chest-pass action from a stable seated position.
Throws were performed separately with the dominant and non-dominant arms, using a coordinated movement involving the trunk and upper-limb musculature.
Throwing distance was determined as the linear distance between the starting line and the first point of ball contact with the floor, measured with a tape measure.
Three maximal attempts were completed with each arm, with 1 minute of recovery between trials.
The greatest distance achieved with each arm was retained for subsequent statistical analyses.
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Baseline and after 6 weeks of resistance 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)
4 de septiembre de 2024
Finalización primaria (Actual)
6 de marzo de 2025
Finalización del estudio (Actual)
6 de marzo de 2025
Fechas de registro del estudio
Enviado por primera vez
11 de junio de 2026
Primero enviado que cumplió con los criterios de control de calidad
11 de junio de 2026
Publicado por primera vez (Actual)
17 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
17 de junio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
11 de junio de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- UGR-TRG-CLG-2024
- 25KJA180002 (Otro número de subvención/financiamiento: Major Project of Basic Science (Natural Science) Research in Jiangsu Higher Education Institutions)
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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