The Effect of Plyometric Training in Freestyle Adolescent Wrestlers

August 12, 2024 updated by: Talha gökçe, Hasan Kalyoncu University

The Effect of Plyometric Exercises on Physical Fitness Parameters in Freestyle Adolescent Wrestlers

This study aims to determine the effect of plyometric exercises on physical fitness parameters in freestyle adolescent wrestlers.

Study Overview

Status

Recruiting

Conditions

Detailed Description

Plyometric exercises are an effective training method that converts strength gains into power by applying specific power (explosive force) training. Plyometric training also dramatically contributes to converting acquired strength into wrestling-specific power. In light of this information, the relatively scarce literature on plyometric training with wrestlers, particularly adolescent freestyle wrestlers, will be studied. This study examines the effects of different plyometric training on physical fitness parameters in adolescent freestyle wrestlers over eight weeks.

The investigators will involve participants who meet the inclusion criteria and who will be randomly assigned to either the control or training group. The training group will undergo plyometric exercise training twice a week for eight weeks in addition to their regular training program. Conversely, the control group will continue their regular training program without additional interventions. Evaluations will be conducted at the beginning and end of the eight weeks to assess the effects of the plyometric training.

The routine training program for the control group participants includes basic strength training (weightlifting exercises), cardiovascular training (biking, running, sprint training, jogging), technical and tactical training, and match-style wrestling. The plyometric training program will be implemented twice a week for 8 weeks, with the number of sets and repetitions of the exercises adjusted weekly to ensure a progressive and safe training regimen.

The investigators will assess the evaluation criteria at the beginning and end of the 8-week training period, comparing pre- and post-training data and conducting intergroup comparisons. Two measurements will be recorded according to these parameters. By the end of the study, the investigators will provide a comprehensive analysis of the impact of the plyometric training program on the physical fitness parameters of freestyle adolescent wrestlers, supported by robust data.

Study Type

Interventional

Enrollment (Estimated)

40

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 Contact

Study Contact Backup

Study Locations

      • Kahramanmaraş, Turkey, 46050
        • Recruiting
        • Batipark Sports Hall
        • Contact:

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

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria for the study:

  • Individuals engaged in freestyle wrestling sport with a valid license,
  • Aged between 10 and 15 years old,
  • Have been practicing this sport for at least three years,
  • Not involved in any other sports discipline,
  • Willing to cooperate and volunteer for the study,
  • The research will include those who have not received medical treatment in the last three months and will not receive treatment during the study period.

Exclusion criteria for the study:

  • Individuals with injuries and chronic pain,
  • Smokers,
  • Regular medication users,
  • Those with neurological and systemic diseases,
  • Individuals who have experienced trauma and undergone surgery in the last three months,
  • Athletes who withdraw their voluntary participation

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Training Group

The training group will receive a carefully designed plyometric training program by a qualified and experienced physiotherapist. This program will be implemented twice a week for eight weeks, with the number of sets and repetitions of the exercises adjusted weekly to ensure a progressive and safe training regimen. Evaluations will be conducted at the beginning and end of the eight weeks to assess the effects of the plyometric training.

Plyometric training program:

  • Vertical jumps
  • Tuck jumps
  • Two-legged broad jumps
  • One-legged bounding
  • Depth jumps from a 40 cm height

Rest intervals between repetitions and sets were set at 15-30 seconds. A 20-minute warm-up period before the program and a 20-minute cool-down period afterwards were planned.

The training group will perform plyometric exercises for eight weeks in addition to their regular training program.
Experimental: Control Group
The control group will continue their regular training program without additional interventions. The routine training program for the control group includes basic strength training (weightlifting exercises), cardiovascular training (biking, running, sprint training, jogging), technical and tactical training, and match-style wrestling. Evaluations will be conducted at the beginning and end of the eight weeks.
The control group's regular training includes basic strength training, cardiovascular training, technical and tactical training, and match-style wrestling.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline in Strength at 8 weeks
Time Frame: Baseline, 8 weeks

Hand Grip Strength Test: Grip strength is a measurement method to evaluate overall body strength and upper extremity performance. This test measures the maximum isometric contraction strength of the hand and forearm muscles. It will be conducted using a hand-grip dynamometer.

Back and Leg Strength Test: This test assesses the strength of the back and leg muscles. It is performed using a back-leg dynamometer.

Baseline, 8 weeks
Change from Baseline in Endurance at 8 weeks
Time Frame: Baseline, 8 weeks

The McGill Core Endurance Test, which consists of four positions (Trunk Flexors Endurance Test, Trunk Extensors Endurance Test, and Right and Left Lateral Plank Tests), will measure participants' endurance. The maximum time each participant can remain in these positions will be recorded in seconds.

Collectively, these tests evaluate the endurance and strength of various core muscles.

Baseline, 8 weeks
Change from Baseline in Agility at 8 weeks
Time Frame: Baseline, 8 weeks
Agility will be measured using the Agility T-Test. This test is set up in a T-shape with four contact points, covering a 10-meter length and width area. Participants must complete a series of movements between these contact points in different directions and patterns as quickly as possible. What sets this test apart from other agility tests is that the participant always faces the same direction. Changes in direction are made by sidestepping to the right and left or by running backward.
Baseline, 8 weeks
Change from Baseline in Wrestling Performance at 8 weeks
Time Frame: Baseline, 8 weeks

Wrestling performance will be measured using a special judo fitness test. The test consists of three application sections of 15, 30, and 30 seconds each, with 10-second rest intervals between applications. In each section, the judoka (tori) must throw the other two judokas (uke) as quickly as possible using the ipon-seoi-nage technique. The distance between the ukes is 6 meters, and the tori starts the applications at 3 meters from each uke.

Participants' heart rates (HR) are recorded immediately after the test (HR_post) and one minute later (HR_1 min). The throws and HR are recorded at the end of the test.

The scoring index for this test is a combination of your post-test and 1-minute later heart rates, divided by the total number of throws. The formula is as follows: Index score = (HR_post + HR_1 min) / throws (total).

Baseline, 8 weeks

Collaborators and Investigators

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

Investigators

  • Study Director: Aysenur Tuncer, PhD, Hasan Kalyoncu University

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)

October 1, 2023

Primary Completion (Estimated)

October 1, 2024

Study Completion (Estimated)

November 15, 2024

Study Registration Dates

First Submitted

April 15, 2024

First Submitted That Met QC Criteria

April 15, 2024

First Posted (Actual)

April 18, 2024

Study Record Updates

Last Update Posted (Actual)

August 14, 2024

Last Update Submitted That Met QC Criteria

August 12, 2024

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2022/118

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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