- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06522802
The Effect of Wearing a Mask for Balance and Reaction Time
July 22, 2024 updated by: yasin yildirim, Istanbul Medipol University Hospital
Does Wearing a Mask Affect Balance and Reaction Time?
A mask is a protective equipment that covers the mouth and nose and is routinely used in workplaces, public transport and other communal settings preventing harmful particles, dust, droplets, bacteria, viruses, fog, gas, smoke and steam from entering the respiratory system.
However, wearing a mask may impair the visual field, potentially affecting balance and reaction time.
The investigators' aim is to determine whether the use of masks affects people's balance and reactions.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
25
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
-
-
Beykoz
-
Istanbul, Beykoz, Turkey
- İstanbul Medipol 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:
- To be healthy
Exclusion Criteria:
- present or previous balance disorder
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: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Evaluation Arm
Only one group evaluated
|
Only 3 tests were applied to participants
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional reach test
Time Frame: baseline-5 hours later
|
Functional Reach Test (FRT) is a clinical outcome measure and assessment tool for ascertaining dynamic balance in in simple task.
As we know that this test measures the distance between the length of an outstretched arm in a maximal forward reach, while maintaining a fixed base of support.
|
baseline-5 hours later
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
COP displacement
Time Frame: baseline-5 hours later
|
Displacement of the center of pressure (COP) and center of gravity (COG) a: COP ML displacement.
Distance of the inflection point from a stationary baseline.
b: Maximum ML separation.
Maximum distance between the COP and COG.
Source publication.
|
baseline-5 hours later
|
|
BlazePod evaluation
Time Frame: baseline-5 hours later
|
A new technology (BlazePod™) that measures response time (RT) is currently on the market and has been used by strength and conditioning professionals.
|
baseline-5 hours later
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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 (Actual)
December 8, 2020
Primary Completion (Actual)
May 30, 2021
Study Completion (Actual)
January 10, 2022
Study Registration Dates
First Submitted
July 12, 2024
First Submitted That Met QC Criteria
July 22, 2024
First Posted (Actual)
July 26, 2024
Study Record Updates
Last Update Posted (Actual)
July 26, 2024
Last Update Submitted That Met QC Criteria
July 22, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 10840098-772.02-E.43565
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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