The Effect of Whole Body Vibration Training on Trunk Muscle Strength, Body Composition and Performance Parameters

December 4, 2023 updated by: Ali ZORLULAR, Gazi University

The Effect of 6-week Whole Body Vibration Training on Trunk Muscle Strength, Body Composition and Performance Parameters

Whole body vibration (WBV) trainings are widely used in the field of sports medicine and rehabilitation. It is accepted that these trainings are a modality that can safely increase muscular activation and performance. However, although many exercise models have been tried on vibration platforms, a standard WBV program for trunk muscles has not been established. A total of 45 healthy individuals will be included in the study. Participants will be divided into 3 groups. Group 1 will perform exercises at 40hz frequency, group 2 will perform exercises at 25hz frequency on WBV. The control group will perform the same exercises at 0 Hz. The training will last 6 weeks and each session consists of 5 exercises.The training consists of basic core exercises that the individual does with his or her own body weight. Each training session is approximately 30 minutes. All participants will be evaluated using an isokinetic strength test with a Cybex dynamometer at the beginning and at the end of the additional treatment protocol. In addition, balance, body composition and anaerobic performance of individuals will be evaluated.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

45

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

      • Ankara, Turkey
        • Gazi University

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

20 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy adults
  • The age range should be between 20-35

Exclusion Criteria:

  • Having an orthopedic problem
  • Having orthopedic surgery in the last 6 months
  • Doing daily exercise and sport

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: 40 hz frequency exercise group
Individuals in this study group will receive exercise training at 40 hz frequency on whole body vibration device.
Participants will be included in the 6-week exercise training on whole body vibration
Experimental: 25 hz frequency exercise group
Individuals in this study group will receive exercise training at 25 hz frequency on whole body vibration device.
Participants will be included in the 6-week exercise training on whole body vibration
Active Comparator: 0 hz frequency exercise group
Individuals in this study group will receive exercise training at 0 hz frequency on whole body vibration device.
Participants will be included in the 6-week exercise training on whole body vibration

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle Strength Assesment
Time Frame: 20 Minutes
Muscle Strength Assesment will be evaluated using isokinetic dynamometer
20 Minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Balance Assesment
Time Frame: 12 Minutes
Posturography will be used to assess static balance
12 Minutes
Body Composition Assesment
Time Frame: 3 Minutes
Body Composition will be evaluated using bioelectrical impedance analyzer
3 Minutes
Anaerobic Power Assesment
Time Frame: 5 Minutes
Anaerobic Power will be evaluated using 3D accelerometer
5 Minutes

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Ali Zorlular, Msc, Gazi 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)

May 17, 2021

Primary Completion (Actual)

December 17, 2021

Study Completion (Actual)

December 30, 2021

Study Registration Dates

First Submitted

August 4, 2021

First Submitted That Met QC Criteria

August 13, 2021

First Posted (Actual)

August 20, 2021

Study Record Updates

Last Update Posted (Actual)

December 5, 2023

Last Update Submitted That Met QC Criteria

December 4, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2020-438

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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