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N95 Masks for Lung Health While Golfing During Wildfire Season

A Pilot / Feasibility Study on Cardiorespiratory Health of Golfers During Wildfire Season

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07620691
Enrollment
40
Registered
2026-06-02
Start date
2026-05-26
Completion date
2026-12-31
Last updated
2026-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchial Asthma

Brief summary

Lung health is negatively affected during wildfire season by increased smoke pollution. Wearing N95 masks protects lung health in the short-term. The purpose of our study is to assess whether wearing of N95 facemasks on days with moderate to high air pollution in people who go outside to golf on a regular basis (two or more times per week) for two months during the wildfire season projects lung health.

Detailed description

Wildfire smoke negatively affects lung health. Across North American, millions of people are exposed to wildfire smoke most summers. The purpose of our study is to determine whether people who golf regularly (two or more times per week) can use N95 masks to protect their lungs from wildfire smoke. Forty regular golfers will be randomized to receive N95 masks or not to receive masks. All participants will be told to follow guidelines for outdoor activity based on Air Quality Health Index readings. Those randomized to wear N95 facemasks will be asked to wear these on days they golf where Air Quality Health Index indicates moderate risk or higher. The main outcome is compliance with wearing the N95 mask. Secondary outcomes include changes in lung function, blood pressure, and respiratory symptoms over two months.

Interventions

DEVICEN95 mask

N95 mask to be worn outside when golfing when Air Quality Health Index reading indicates moderate risk or higher

Sponsors

University of Saskatchewan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Participants are blinded to the hypothesis of the study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Golf on a regular basis (two or more times per week)

Exclusion criteria

* Smoker

Design outcomes

Primary

MeasureTime frameDescription
Change in compliance with wearing of N95 masks (number of times divided by days with moderate or higher air pollution)8 weekscompliance with wearing the N95 masks

Secondary

MeasureTime frameDescription
Change in forced expiratory volume in one second (L)8 weeksForce expiratory volume in one second measured with spirometry
Change in forced vital capacity (mL)8 weeksForced vital capacity measured by spirometry
Change in forced expiratory flow at 25% to 75% of vital capacity (mL)8 weeksforced expiratory flow at 25% to 75% of vital capacity measured by spirometry
Change in respiratory symptoms (score out of 12)8 weeksRespiratory symptoms determined by the Dyspnoea-12 questionnaire
Change in systolic blood pressure (mmHg)8 weeksSystolic blood pressure measured by an automatic sphygmomanometer
Change in diastolic blood pressure (mmHg)8 weeksDiastolic blood pressure measured by an automatic sphygmomanometer

Countries

Canada

Contacts

CONTACTPhilip Chilibeck, PhD
phil.chilibeck@usask.ca3062303849
PRINCIPAL_INVESTIGATORPhilip Chilibeck, PhD

University of Saskatchewan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026