- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04012762
Vibration Training and Muscles Properties (CT)
July 8, 2019 updated by: Tülay Çevik
The Acute Responses of Muscles Properties to the Different Whole Body Vibration Training
Application dose standards have not yet been determined for Whole Body Vibration Training which is subject to studies with different frequencies and amplitudes.
Our objective was to examine acute responses of two different vibration training doses on muscle tone, strength, and flexibility.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Application dose standards have not yet been determined for Whole Body Vibration Training which is subject to studies with different frequencies and amplitudes.
Our objective was to examine acute responses of two different vibration training doses on muscle tone, strength, and flexibility.
Study Type
Interventional
Enrollment (Actual)
50
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
-
-
İ̇stanbul
-
Tuzla, İ̇stanbul, Turkey, 34959
- Okan 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
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy and untrained participants.
- Dominant side of the participants was recorded and only right dominant individuals were included.
Exclusion Criteria:
- Participants with body weight over 120 kg.
- Participants had lower extremity trauma and lower extremity movement restriction.
- Participants who had any cardiovascular or neurological conditions, dizziness or vertigo
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: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Moderate-intensity group
WBVT application was 2-4 mm for vibration amplitude value and 25 Hz for training frequency in moderate-intensity group.
|
Intermittent whole-body vibration exposure is a training method providing physical stimulation effect on skeletal muscles by increasing gravitational acceleration on the vibration platform.
|
Active Comparator: Vigorous-intensity group
WBVT application was 2-4 mm for vibration amplitude value and 40 Hz for training frequency in vigorous-intensity group.
|
Intermittent whole-body vibration exposure is a training method providing physical stimulation effect on skeletal muscles by increasing gravitational acceleration on the vibration platform.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle Tone
Time Frame: 30 minute
|
Tone assessments were made by MyotonPro Digital Palpation Device.
|
30 minute
|
Muscle power
Time Frame: 30 minute
|
The muscle power evaluation was made by Lafayette Manuel Muscle Testing System.
|
30 minute
|
Flexibility
Time Frame: 30 minute
|
Hamstring flexibility was evaluated with Sit and Reach Test.
|
30 minute
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Emine Atıcı, Ph. D., Istanbul Okan Univesitesi
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 15, 2019
Primary Completion (Actual)
July 5, 2019
Study Completion (Actual)
July 8, 2019
Study Registration Dates
First Submitted
July 8, 2019
First Submitted That Met QC Criteria
July 8, 2019
First Posted (Actual)
July 9, 2019
Study Record Updates
Last Update Posted (Actual)
July 10, 2019
Last Update Submitted That Met QC Criteria
July 8, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- Bitlis Eren University
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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