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Cluster-Set vs. Traditional-Set Plyometric Loading in Tennis Players (TENNIS_CLS-TRD)

5 giugno 2026 aggiornato da: Ramiz ARABACI, Uludag University

Acute Effects of Cluster-Set vs. Traditional-Set Plyometric Loading on Countermovement Jump and Reactive Strength Index in Young Tennis Players

The present study aimed to compare the acute effects of cluster-set (CS) and traditional-set (TS) plyometric loading protocols on countermovement jump (CMJ) performance and reactive strength index (RSI-mod) in young tennis players.

Twenty-eight male tennis players (age: 16.7 ± 1.3 years) were randomly assigned to either a CS or TS group. Following a familiarization session, participants completed an experimental session including pre-tests (CMJ and drop jump), a plyometric loading protocol (CS: 3 × [5 × 2 repetitions, 15 s intra-set rest, 2 min between sets]; TS: 3 × 10 repetitions, 3 min between sets), and post-tests at 15 s, 3 min, and 6 min. CMJ height and RSI-mod were assessed using the My Jump 2 application. Borg Scale, Total Quality Recovery (TQR) were apply after post-tests at 15 s, 3 min, and 6 min.

Panoramica dello studio

Stato

Completato

Condizioni

Descrizione dettagliata

The present study aimed to compare the acute effects of cluster-set (CS) and traditional-set (TS) plyometric loading protocols on countermovement jump (CMJ) performance and reactive strength index (RSI-mod) in young tennis players. It was hypothesized that the CS method would elicit superior acute improvements in jump parameters and recovery due to reduced fatigue compared to the TS method. A total of 28 male adolescent tennis players, aged 13-17 years, voluntarily participated. Volunteers were randomly allocated into two experimental groups: Cluster Set Group (CS) and Traditional Set Group (TS). ). Participants were eligible if they met the following criteria.

i. Engaged in tennis training for ≥2 years, with a frequency of ≥3 sessions/week and participation in ≥4 tournaments annually.

ii. Had ≥6 months of experience with resistance and plyometric training. iii. No history of lower extremity muscle or joint injuries within the last three months.

iv. No regular use of drugs or stimulants for at least six months prior to the study.

The study consisted of two sessions: a familiarization session and an experimental session involving either the Cluster Set (CS) or Traditional Set (TS) protocol. Participants refrained from any exhaustive exercise for at least 48 hours prior to the familiarization session, and a 48-hour passive recovery period was observed between sessions. During the familiarization session, anthropometric measurements (height, body mass, body fat %) were recorded, and participants completed the Physical Activity Readiness Questionnaire (PAR-Q+). Following this, subjects performed a standardized warm-up and familiarization with the testing procedures. The experimental session included the following sequence: (i) Pre-test measurements: Countermovement Jump (CMJ) and Drop Jump (DJ), (ii) execution of either CS or TS plyometric protocol, (iii) immediate Post-15s): CMJ and DJ, (iv) passive recovery (3 min) followed by CMJ and DJ, and assessment using the Total Recovery Quality Scale (TQR), (v) additional passive recovery (3 m) followed by CMJ and DJ and TQR, (vi) final post-test (6 min): CMJ and DJ. Total workout 7 minutes and passive rest 6 minutes (Table 2). Participants were instructed to sleep at least 8 hours the night before testing. Maintain a normal diet and avoid medications, stimulants, ergogenic aids, or performance-enhancing substances. Before testing, all participants completed a 10-minute standardized warm-up, consisting of jogging, galloping, multidirectional running and jumping, calisthenic exercises for joint mobility, static and dynamic stretching. The procedure of the study is shown in Figure 1. All interventions were conducted between 15:00 and 17:00 in a synthetic-floored gym under controlled conditions (temperature: 18-24°C; humidity: 40-60%). Two Way ANOVA repeated measures analysis of variance, 2 groups (CS and TS) x 4 time (Pre, Post-15s; Post-3m and Post-6m) test was performed to compare the data and determine the differences. Bonferroni test was used for pairwise time and group comparisons.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

28

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Bursa, Turchia (Türkiye), 16059
        • Bursa uludag University, Faculty of Sport Sciences

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Engaged in tennis training for ≥2 years, with a frequency of ≥3 sessions/week and participation in ≥4 tournaments annually.
  • Had ≥6 months of experience with resistance and plyometric training.
  • No history of lower extremity muscle or joint injuries within the last three months.
  • No regular use of drugs or stimulants for at least six months prior to the study.

Exclusion Criteria:

-

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Cluster Set Plyometric Loading
Cluster set: plyometric jumping 3 set , each set consist of 2 repetition x 5.
Cluster Set: Vertical Jumping 3 set, 2 minute rest/set, in 1 set 5 x 2 repetition, 15 sec rest after each 2 repetition.
Comparatore attivo: Traditional Set Plyometric Loading
Traditional set: pluometric jumping 3 set, each set consist of 10 repetition.
Traditional set: Vertical jumping 3 set, 3 minute rest / set, in 1 set 10 repetition/set

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Vertical Jump
Lasso di tempo: From enrollment to the end of treatment at 15 days
The counter movement jump (CMJ) test was used to determine vertical jump height. CMJ is widely used to monitor neuromuscular status (i.e. fatigue, performance, strength, and muscle overcompensation) from the analysis of bilateral mechanics and the ability to generate and the ability to generate and absorb ground reaction forces by the lower extremity. The My Jump 2 (Copyright©Carlos Balsalobre Fernández) application of the My Jump Lab tools, based on artificial intelligence (AI) used to measure CMJ. An iPad Pro 11-inch Model Air M2 (Apple Inc. Cupertino, CA) used to capture each trial.
From enrollment to the end of treatment at 15 days
Vertical Jump
Lasso di tempo: From enrollment to the end of treatment at 15 days
The counter movement jump (CMJ) test was used to determine vertical jump high. The My Jump 2 (Copyright©Carlos Balsalobre Fernández) application of the My Jump Lab tools, based on artificial intelligence (AI) used to measure CMJ. An iPad Pro 11-inch Model Air M2 (Apple Inc. Cupertino, CA) used to capture each trial.
From enrollment to the end of treatment at 15 days
Reactive Strength Index (RSI-mod)
Lasso di tempo: From enrollment to the end of treatment at 15 days
The Drop Jump (DJ) test was used to determine the RSI-mod. The DJ can be used to determine the intensity of plyometric exercises, measure lower body reactive strength, monitor neuromuscular fatigue and test lower extremity stiffness. The DJ is a frequently analyzed metric for determining the RSI. It assesses an athlete's ability to rapidly transition from eccentric to concentric contraction and how much force the athlete can produce in the shortest possible time. There are multiple calculations available to measure the RSI-mod, but the most used is jump height (meters) ÷ ground contact time (seconds). Participants were asked to perform the DJ test by dropping to the ground from a 40 cm frame height with their hands on their hips and jumping upwards with maximal effort in the shortest time. Vertical jump distance and RSI were determined using the My Jump 2 app.
From enrollment to the end of treatment at 15 days

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Body composition
Lasso di tempo: From enrollment to the end of treatment at 15 days
Participants' body weight and body fat percentage were assessed using a Tanita BC-418 bioelectrical impedance analyzer (Tanita Corp., Tokyo, Japan). Height was measured with a Seca stadiometer (Seca Instruments Ltd., Hamburg, Germany).
From enrollment to the end of treatment at 15 days
Recovery
Lasso di tempo: From enrollment to the end of treatment at 15 days
Recovery perception was evaluated using the Turkish version of the Total Quality Recovery (TQR) scale. This scale ranges from 6 points ("very poor recovery") to 20 points ("very good recovery"). Participants completed the TQR at the end of each 3-minute passive rest period following Post-15s and Post-3m jump tests.
From enrollment to the end of treatment at 15 days

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Ramiz ARABACI, Prof.Dr., Bursa uludag University, Faculty of Sport Sciences

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

15 marzo 2025

Completamento primario (Effettivo)

30 marzo 2025

Completamento dello studio (Effettivo)

15 aprile 2025

Date di iscrizione allo studio

Primo inviato

2 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

5 giugno 2026

Primo Inserito (Effettivo)

11 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

11 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

5 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • Date10.01.2025, Approval No460

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

All IPD collected throughout the trial, only IPD used in the results publication.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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