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- Ensaio Clínico NCT07653425
Traditional Versus Cluster Resistance Training in Striking Combat Sport Athletes (TRG-CLG)
11 de junho de 2026 atualizado 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.
Visão geral do estudo
Status
Concluído
Condições
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Real)
32
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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Concepción, Chile
- Universidad Católica de la Santísima Concepción
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
Aceita Voluntários Saudáveis
Sim
Descrição
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.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Ciência básica
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Comparador Ativo: 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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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Load-velocity relationship (LVR).
Prazo: 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 resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Countermovement jump
Prazo: 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).
Prazo: 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
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Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
4 de setembro de 2024
Conclusão Primária (Real)
6 de março de 2025
Conclusão do estudo (Real)
6 de março de 2025
Datas de inscrição no estudo
Enviado pela primeira vez
11 de junho de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
11 de junho de 2026
Primeira postagem (Real)
17 de junho de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
17 de junho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
11 de junho de 2026
Última verificação
1 de junho de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- UGR-TRG-CLG-2024
- 25KJA180002 (Número de outro subsídio/financiamento: Major Project of Basic Science (Natural Science) Research in Jiangsu Higher Education Institutions)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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