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

5 de junio de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

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 de estudio

Intervencionista

Inscripción (Actual)

28

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño

Acepta Voluntarios Saludables

Sí

Descripción

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:

-

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Comparador activo: 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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Vertical Jump
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Body composition
Periodo de tiempo: 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
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de marzo de 2025

Finalización primaria (Actual)

30 de marzo de 2025

Finalización del estudio (Actual)

15 de abril de 2025

Fechas de registro del estudio

Enviado por primera vez

2 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

5 de junio de 2026

Publicado por primera vez (Actual)

11 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

11 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

5 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • Date10.01.2025, Approval No460

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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