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

11 czerwca 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Zakończony

Warunki

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

32

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

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

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły

Akceptuje zdrowych ochotników

Tak

Opis

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 studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Podstawowa nauka
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny 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.
Behawioralne: 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.
Eksperymentalny: 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.
Behawioralne: 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.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Load-velocity relationship (LVR).
Ramy czasowe: 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

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Countermovement jump
Ramy czasowe: 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).
Ramy czasowe: 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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Universidad de Granada

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

4 września 2024

Zakończenie podstawowe (Rzeczywisty)

6 marca 2025

Ukończenie studiów (Rzeczywisty)

6 marca 2025

Daty rejestracji na studia

Pierwszy przesłany

11 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

11 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

17 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

17 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

11 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Inne numery identyfikacyjne badania

  • UGR-TRG-CLG-2024
  • 25KJA180002 (Inny numer grantu/finansowania: Major Project of Basic Science (Natural Science) Research in Jiangsu Higher Education Institutions)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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