- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05014958
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
Intervention / Treatment
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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