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

11. Juni 2026 aktualisiert von: 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.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Tatsächlich)

32

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Chile
      • Concepción, Chile
        • Universidad Católica de la Santísima Concepción

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Grundlegende Wissenschaft
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Single

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Aktiver Komparator: 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.
Verhalten: Traditional
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.
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.
Verhalten: Cluster
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Load-velocity relationship (LVR).
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Countermovement jump
Zeitfenster: 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).
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Universidad de Granada

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

4. September 2024

Primärer Abschluss (Tatsächlich)

6. März 2025

Studienabschluss (Tatsächlich)

6. März 2025

Studienanmeldedaten

Zuerst eingereicht

11. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. Juni 2026

Zuerst gepostet (Tatsächlich)

17. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

17. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Andere Studien-ID-Nummern

  • UGR-TRG-CLG-2024
  • 25KJA180002 (Andere Zuschuss-/Finanzierungsnummer: Major Project of Basic Science (Natural Science) Research in Jiangsu Higher Education Institutions)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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