Effects of Ballistic vs Plyometric Training on Performance of Badminton Players (EBVPB)

January 22, 2025 updated by: Riphah International University

Ballistic and plyometric training are both frequently utilized to enhance physical performance in a variety of sporting activities that require the ability to jump, sprint, and change direction. both are designed to improve explosive power, but they differ in their approaches and focus. Although many studies highlight the significance of both plyometric and ballistic exercises in enhancing athletic performance in badminton players no direct comparison has been made between the two.

In this study we compared the effectiveness of Ballistic exercises versus Plyometric exercises on performance in Badminton players, which is going to help us to select the best possible training program for badminton athletes

Study Overview

Status

Not yet recruiting

Detailed Description

Ballistic and plyometric training are both frequently utilized to enhance physical performance in a variety of sporting activities that require the ability to jump, sprint, and change direction. both are designed to improve explosive power, but they differ in their approaches and focus. Although many studies highlight the significance of both plyometric and ballistic exercises in enhancing athletic performance in badminton players no direct comparison has been made between the two.

In this study we compared the effectiveness of Ballistic exercises versus Plyometric exercises on performance in Badminton players, which is going to help us to select the best possible training program for badminton athletes

Study Type

Interventional

Enrollment (Estimated)

60

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 Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Liaqat Bagh Stadium Rawalpindi

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria

  • Active Badminton player.
  • Age between 20-28 years.
  • Male Badminton players

Exclusion Criteria

  • Athletes with injuries, trauma, pathology, any neurological or psychological complications.
  • Athletes with Metabolic diseases.
  • Age above 28 years or less than 20.
  • Other than male Players.

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
Other: Ballistic group
Ballistic training program was set for 6 weeks. Each week consisting of 5 exercises with sets of 3 and repetitions of 10,15 and 20 times, recovery time and training intensity differed each week.
Ballistic training program was set for 6 weeks. Each week consisting of 5 exercises with sets of 3 and repetitions of 10,15 and 20 times, recovery time and training intensity differed each week.
Experimental: Plyometric Group
Plyometric training program was set for 6 weeks. With four exercises in 1st week. Five in 2nd and 3rd weeks, six exercises in 4th and seven exercises in last two weeks. Each exercise consisted of 3 sets with 10, 15 and 20 repetitions in each. Recovery time and training intensity differed each week.
Plyometric training program was set for 6 weeks. With four exercises in 1st week. Five in 2nd and 3rd weeks, six exercises in 4th and seven exercises in last two weeks. Each exercise consisted of 3 sets with 10, 15 and 20 repetitions in each. Recovery time and training intensity differed each week.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Push up test
Time Frame: six weeks
The Test demanded that the test subject lie face down on the floor with their elbows pointing backward down their side, their hands beneath their shoulders, and their fingers pointing forward. The individual's body weight rested on their hands and toes after pushing themselves to full arm extension; The up position was this. Then, maintaining a straight body, the person lowered himself until the entire body, from the chest to the thighs, made contact with the ground. Then the participants returned to the up position after being pulled up to full arm extension. One push-up test was made up of these up and down steps. from enrollment to the end of treatment up to six weeks
six weeks
Closed kinetic chain upper extremity stability test
Time Frame: six weeks
On a tiled floor, athletic tape strips were positioned 36 inches apart and parallel to one another. The test began with one hand in the push-up position on each piece of tape. From the beginning, the patients were told to reach across their body with one hand and touch the piece of tape underneath the other hand. The hand was put back in the beginning position after touching the tape line. The patient then used the other hand to make the same motion. The testing lasted 15 seconds in total. from enrollment to the end of treatment up to six weeks
six weeks
Seated medicine ball throw test
Time Frame: six weeks
Each athlete started the test by holding the 2 kg medicine ball with both hands, resting it firmly against their chest. The task was to throw the ball forward as far as possible using a chest press motion, a movement that primarily engages the chest, shoulders, and arms in an effort to achieve maximum distance. from enrollment to the end of treatment up to six weeks
six weeks
Unilateral single arm shot put test
Time Frame: six weeks
To evaluate upper body strength and power, a 3-kilogram medicine ball was used. On the floor, athletes sat with their feet flat, knees bent at a 90-degree angle, and backs against the wall on the floor for stability. They were positioned next to a doorway to allow unrestricted arm movement on the test side. The participants were instructed to hold the medicine ball at shoulder height and push it forward-rather than throwing it-using an explosive chest press motion to propel it as far as possible. from enrollment to the end of treatment up to six weeks
six weeks

Collaborators and Investigators

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

Investigators

  • Study Director: Dr Nadia Ishtiaq, MS, Riphah International University

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 (Estimated)

February 3, 2025

Primary Completion (Estimated)

April 10, 2025

Study Completion (Estimated)

May 10, 2025

Study Registration Dates

First Submitted

January 10, 2025

First Submitted That Met QC Criteria

January 22, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 22, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Nadia Ishtiaq

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

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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