- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06172244
Acute Effect of Whole Body Vibration on Reaction Speed and Proprioception
April 1, 2024 updated by: Çağtay Maden
Acute Effect of Whole Body Vibration on Reaction Speed and Proprioception in the Upper Extremity in Healthy Subjects
It will be determined whether the application of whole body vibration has an immediate effect on upper extremity reaction speed and proprioception.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Muscles and tendons are among the mechanisms affected by whole body vibration.
In this way, it is thought that TVV indirectly affects the reaction speed of individuals.
In the light of this information, this study was planned to investigate how whole body vibration application affects proprioception and reaction speed.
The reaction rate and instantaneous effect of the virion given at 30 Hz and 2 mm amplitude in the push-up position on proprioception will be investigated.
The aim of this study is to investigate the instantaneous effect of whole body vibration on reaction speed and proprioception in the upper extremity in healthy individuals.
Study Type
Interventional
Enrollment (Actual)
62
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
-
-
Şahinbey
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Gaziantep, Şahinbey, Turkey, 27000
- Gaziantep Islamic Science and Technology 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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Healthy individuals between the ages of 18-25
- Those who do not have any orthopedic problems in the upper extremity
- Individuals without any neurological problems
- Those who volunteer to participate in the study
Exclusion Criteria:
- Those who have 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: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Whole body vibration
A total of 5 sets of vibration will be given at 30 Hz, 2 mm amplitude, 1 minute of application and 1 minute of rest.
|
A total of 5 sets of vibration will be given at 30 Hz, 2 mm amplitude, 1 minute of application and 1 minute of rest.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nelson Hand Reaction Test
Time Frame: All measurements take 30 minutes for each individual, before and immediately after the application on the same day.
|
The participant is asked to sit in the chair with the forearm and hand comfortably resting on the table.
The tips of the thumb and index finger are positioned 8-10 cm away from the table, with the tops of the thumb and index finger parallel to each other.
The tester asks the individual to hold the ruler between his thumb and index finger.
At the same time, the patient is asked to look directly at the middle point of the ruler while holding it between his fingers.
As soon as the ruler is released, the person is told to catch the ruler with his thumb and forefinger.
The ruler is left and the numerical value on the upper edge of the subject's thumb, where the subject grasps the ruler, is read and recorded.
|
All measurements take 30 minutes for each individual, before and immediately after the application on the same day.
|
|
Reaction Rate Evaluation with Sway Medical Smartphone Application
Time Frame: All measurements take 30 minutes for each individual, before and immediately after the application on the same day.
|
The person will sit comfortably on a chair and hold the smartphone with the thumbs on both sides.
When the orange screen appears, the phone should quickly rotate the screen in the desired direction.
Once you will do the test to learn the application.
Then, the application is made three times and the reaction rate is calculated by taking the average time of these three applications.
|
All measurements take 30 minutes for each individual, before and immediately after the application on the same day.
|
|
Upper extremity proprioception measurement
Time Frame: All measurements take 30 minutes for each individual, before and immediately after the application on the same day.
|
Elbow flexion, shoulder flexion and abduction 30 and 60 degree angles were measured with a digital goniometer.
The elbow and shoulder positions were brought to the desired angle and they were asked to return to the same angle.
The angle of deviation was recorded.
|
All measurements take 30 minutes for each individual, before and immediately after the application on the same day.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Çağtay MADEN, Gaziantep Islamic Science and Technology 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)
July 1, 2023
Primary Completion (Actual)
November 1, 2023
Study Completion (Actual)
November 30, 2023
Study Registration Dates
First Submitted
December 7, 2023
First Submitted That Met QC Criteria
December 7, 2023
First Posted (Actual)
December 15, 2023
Study Record Updates
Last Update Posted (Actual)
April 2, 2024
Last Update Submitted That Met QC Criteria
April 1, 2024
Last Verified
June 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 2023/266
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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