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

2026年6月5日 更新者: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.

研究概览

详细说明

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.

研究类型

介入性

注册 (实际的)

28

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Bursa、土耳其(türkiye)、16059
        • Bursa uludag University, Faculty of Sport Sciences

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

是的

描述

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:

-

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的: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.
有源比较器: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

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Vertical Jump
大体时间: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
大体时间: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)
大体时间: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

次要结果测量

结果测量
措施说明
大体时间
Body composition
大体时间: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
大体时间: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

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Ramiz ARABACI, Prof.Dr.、Bursa uludag University, Faculty of Sport Sciences

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年3月15日

初级完成 (实际的)

2025年3月30日

研究完成 (实际的)

2025年4月15日

研究注册日期

首次提交

2026年6月2日

首先提交符合 QC 标准的

2026年6月5日

首次发布 (实际的)

2026年6月11日

研究记录更新

最后更新发布 (实际的)

2026年6月11日

上次提交的符合 QC 标准的更新

2026年6月5日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • Date10.01.2025, Approval No460

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

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

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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