Effects of a Plyometric Training Program on Youths With Different Biological Maturity in Sport

May 29, 2026 updated by: Jakub Krejci, Palacky University

A Randomized Controlled Trial Evaluating the Effect of Plyometric Training on Power, Speed, and Agility in Sport-active Boys With Different Biological Maturity

This randomized controlled trial aims to assess the effectiveness of a 12-week plyometric training regimen on improving power, speed, and agility among boys aged 10 to 18 years who are actively engaged in sports and exhibit differing levels of biological maturity. The study seeks to determine how maturation affects the responsiveness to the training program, potentially influencing future sports training approaches for young athletes.

Study Overview

Detailed Description

The main objective of this project is to assess the impact of a plyometric program on power, speed, agility, reactive strength index and stiffness in male athletes of different levels of maturation. The study takes the form of a short-term experiment (12 weeks), involving 30 young athletes with a minimum of two years of experience in systematic sports training. Participants are divided into an experimental group and a control group. The experimental group undergoes a 12-week plyometric training program, implemented twice a week within training sessions immediately following warm-ups. The control group engages in technical-tactical exercises. The program is developed by the authors of the research project based on current knowledge and requirements for creating an effective and safe plyometric program. Randomization is performed using a computer random generator. Participants undergo two testing sessions: one prior to the training intervention and the other one week after its completion. Age, height, weight, and body composition are measured using a personal scale with an integrated stadiometer. Tests include a 30-m sprint, countermovement jump, broad jump, unilateral triple jump, drop jump (reactive strength index), 20 submaximal vertical jumps (lower limb stiffness), BlazePod reaction test, and 505 agility test. The maturity status of the participants is evaluated using the Mirwald method and is used as a covariate in the subsequent statistical analysis. Findings of this research may provide crucial insights for targeted integration of plyometric methods during the developmental and maturation phases of young athletes.

Study Type

Interventional

Enrollment (Actual)

38

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Olomouc, Czechia, 77111
        • Palacky University, Faculty of Physical Culture

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Minimum of 2 years of organized sports participation.
  • Good health as confirmed by a pre-study medical screening.
  • Signed informed consent from the legal representative and verbal assent from the participant.

Exclusion Criteria:

  • Any serious lower limb injury in the past 6 months.
  • Any current or historical mental health disorders.
  • Any condition deemed by the medical screener as a contraindication to vigorous physical activity.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Plyometric training
Plyometric training program for 12 weeks.
Participants undergo a plyometric training program. The plyometric training consists of exercises in the horizontal, lateral, and vertical directions of movement. Exercises are progressively focused on maximal performance with short ground contact (<250 ms). The training sessions are twice per week.
Active Comparator: Control training
Regular training program for 12 weeks.
Participants continues their regular sports activities without additional plyometric training. The training sessions are twice per week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical jump height
Time Frame: 12 weeks
The vertical jump is performed on AMTI OR6-7-1000 force platform (Advanced Mechanical Technology, Watertown, USA). Participants stand on the force platform in an upright position and on command, perform a maximum height jump with a countermovement and use of arms. Participants perform three attempts, with a 1-min rest between each. The best attempt is evaluated.
12 weeks
Broad jump distance
Time Frame: 12 weeks
The distance in the broad jump is measured with a tape. Participants stand on a pre-marked line with legs approximately shoulder-width apart. From standing, they jump as far forward as possible using a countermovement and land on both feet. The landing spot closest to the starting line is considered for scoring. Participants perform two attempts, with the better attempt being recorded. There is a 1-min rest between attempts.
12 weeks
Unilateral triple jump length
Time Frame: 12 weeks
The length of the unilateral triple jump test is measured with a tape. Participants start on one leg on a pre-marked line. Then using a countermovement from knee flexion, they perform a triple jump with the dominant and subsequently the non-dominant lower limb. After the final jump, they must land on both limbs and maintain their position at the landing spot for at least 2 seconds.
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Linear speed
Time Frame: 12 weeks
A 20-m sprint test is used to assess linear speed. The final time is recorded using photoelectric cells (Brower Timing System, Draper, USA) with accuracy of 0.01 s. Photocells are placed at the start and 20-m mark. Participants start on command, with timing starting as soon as the player begins to move.
12 weeks
Agility test
Time Frame: 12 weeks
For the 505 agility test, photoelectric cells (PR1aW, ALGE-TIMING, Lustenau, Austria) are used, placed at the 10-m mark. Cones are placed at the 0, 10, and 15-m marks. Participants sprint 10 meters and are instructed to reach maximum speed by the 10-m mark. At the 15-m mark, they perform a 180-degree turn and sprint back to the 10-m mark at maximum speed. Each participant have one attempt on the dominant and one attempt on the non-dominant leg for the 180-degree turn.
12 weeks
Reaction test
Time Frame: 12 weeks
In the BlazePod reaction test (Play Coyotta, Tel Aviv, Israel), 5 sensors are placed parallel, 1 m apart from each other. The participant stand 3 m in front of the middle sensor. When any sensor lights up, the participant must press it as quickly as possible and return to the starting position, waiting for the next sensor to light up. Sensors light up in a random order. The test lasts after 10 attempts.
12 weeks
Lower limb stiffness
Time Frame: 12 weeks
Lower limb stiffness is measured using the repeated submaximal jumps test (Optojump Next, Microgate, Italy). Participants perform 20 repeated jumps at a frequency of 2.5 Hz (mechanical metronome Wittner, Isny, Germany). Participants stand approximately shoulder-width apart with their hands on their sides throughout the test. Participants undergo three attempts with 2-min rest in between.
12 weeks
Reactive strength index
Time Frame: 12 weeks
Reactive strength index is measured using the drop jump on AMTI OR6-7-1000 force platform (Advanced Mechanical Technology, Watertown, USA). Participants stand with feet shoulder-width apart on a platform 30 cm above the floor and have their hands on their sides. Then they step off the platform with one foot and upon landing, rebound as quickly as possible and with maximum effort. Reactive strength index is calculated from the ratio of jump height to the duration of contact with the platform.
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Roman Holik, Mgr, Palacky University, Faculty of Physical Culture

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 13, 2024

Primary Completion (Actual)

August 16, 2024

Study Completion (Actual)

August 16, 2024

Study Registration Dates

First Submitted

May 6, 2024

First Submitted That Met QC Criteria

May 6, 2024

First Posted (Actual)

May 9, 2024

Study Record Updates

Last Update Posted (Actual)

June 2, 2026

Last Update Submitted That Met QC Criteria

May 29, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymised raw data will be made available.

IPD Sharing Time Frame

The data will be available once the results are published in a scientific journal.

IPD Sharing Access Criteria

For everybody.

Study Data/Documents

  1. Individual Participant Data Set
    Information comments: Holík R, Krejčí J, Lehnert M. Dataset for: "The effect of plyometric training on physical performance in youth soccer players: A randomized controlled trial with maturation status as a covariate". Zenodo; 2025.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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