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

5. juni 2026 oppdatert av: 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.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

28

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn

Tar imot friske frivillige

Ja

Beskrivelse

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:

-

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Aktiv komparator: 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

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Vertical Jump
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Body composition
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

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Etterforskere

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

Publikasjoner og nyttige lenker

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Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

15. mars 2025

Primær fullføring (Faktiske)

30. mars 2025

Studiet fullført (Faktiske)

15. april 2025

Datoer for studieregistrering

Først innsendt

2. juni 2026

Først innsendt som oppfylte QC-kriteriene

5. juni 2026

Først lagt ut (Faktiske)

11. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

11. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

5. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • Date10.01.2025, Approval No460

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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

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Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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