Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Traditional Versus Cluster Resistance Training in Striking Combat Sport Athletes (TRG-CLG)

11 juin 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Complété

Type d'étude

Interventionnel

Inscription (Réel)

32

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Concepción, Chili
        • Universidad Católica de la Santísima Concepción

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte

Accepte les volontaires sains

Oui

La description

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 d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: 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.
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.
Expérimental: 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.
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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Load-velocity relationship (LVR).
Délai: Baseline and after 6 weeks of resistance training
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.
Baseline and after 6 weeks of resistance training

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Countermovement jump
Délai: Baseline and after 6 weeks of resistance training
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.
Baseline and after 6 weeks of resistance training
Medicine ball throw (MBT).
Délai: Baseline and after 6 weeks of resistance training
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.
Baseline and after 6 weeks of resistance training

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

4 septembre 2024

Achèvement primaire (Réel)

6 mars 2025

Achèvement de l'étude (Réel)

6 mars 2025

Dates d'inscription aux études

Première soumission

11 juin 2026

Première soumission répondant aux critères de contrôle qualité

11 juin 2026

Première publication (Réel)

17 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

17 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

11 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • UGR-TRG-CLG-2024
  • 25KJA180002 (Autre subvention/numéro de financement: Major Project of Basic Science (Natural Science) Research in Jiangsu Higher Education Institutions)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner