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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04557605
Other study ID # 2201
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 14, 2020
Est. completion date October 15, 2020

Study information

Verified date October 2020
Source University of Saskatchewan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is concern that wearing a face mask during COVID will affect oxygen uptake, especially during intense exercise. This study will assess the effect of wearing two different face masks (disposable and cloth) on blood and muscle oxygenation during cycling exercise.


Description:

There is concern that wearing a face mask during exercise will reduce oxygen uptake or increase carbon dioxide re-breathing, which can result in low blood oxygen levels, reduced oxygen delivery to muscle and reduced exercise capacity. The purpose of the study is to determine the effect of wearing two different types of commonly-worn face masks (diposable and cloth) during exercise on blood and muscle oxygenation. Twelve participants who are experienced with cycling will take part in this randomized cross-over study that will assess blood oxygenation (i.e. pulse oximetry) and muscle oxygenation (with near infrared spectroscopy) during a progressive step exercise test to exhaustion. The conditions include no mask, a disposable mask, and a cloth mask. Outcome variables include exercise duration, rating of perceived exertion, blood oxygen saturation levels, and oxygenated, deoxygenated, and total hemoglobin at the quadriceps muscle.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date October 15, 2020
Est. primary completion date October 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Experienced with cycling Exclusion Criteria: - Contra-indications to exercise as identified by a screening questionnaire (the "Get Active Questionnaire")

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Progressive cycling exercise test to exhaustion
Progressive step cycling exercise test to exhaustion

Locations

Country Name City State
Canada University of Saskatchewan Saskatoon Saskatchewan

Sponsors (1)

Lead Sponsor Collaborator
University of Saskatchewan

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to exhaustion during exercise time to exhaustion Up to 20 minutes
Primary Change from baseline in peak power output Peak power output in Watts, determined on a cycle ergometer Up to 20 minutes
Secondary Change from baseline in blood oxygen saturation Blood oxygen saturation as determined by pulse oximetry Up to 20 minutes
Secondary Change from baseline in quadriceps tissue oxygenation index Tissue oxygenation index (oxygenated hemoglobin/total hemoglobin) as measured by near infra-red spectroscopy Up to 20 minutes
Secondary Change from baseline in rating of perceived exertion Rating of perceived exertion on a scale of 1-10 (Modified Borg Scale), a higher score indicates a greater perceived exertion Up to 20 minutes
Secondary Change from baseline in heart rate Heart rate (beats per minute) Up to 20 minutes
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