ClinicalTrials.Veeva

Menu

Investigating Changes in Responses to Controlled Effective Doses of Ozone at Different Exercise Intensities

M

Michael Koehle

Status

Withdrawn

Conditions

Ozone
Exercise Intensity

Treatments

Behavioral: Heavy Intensity
Other: Filtered Air
Other: Ozone
Behavioral: Moderate Intensity

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The project will look to investigate whether exercise during ozone exposure performed for a shorter duration at a higher intensity is more harmful than exercise performed for a longer duration at a lighter intensity. To assess this, participants will perform these exercise conditions with and without ozone exposure and researchers will assess changes in lung function, subjective symptoms, and breathing mechanics to determine which is more harmful.

Full description

Purpose and Hypothesis The purpose of the study is to investigate whether exercise performed at a higher intensity for a shorter duration during ozone exposure results in greater decrements in pulmonary function, subjective symptoms, and dyspnea than low intensity exercise performed for a longer duration. The researcher's hypothesize that high intensity exercise will result in worsened responses as a result of changes to breathing mechanics resulting in greater penetration of ozone into smaller airways of the lungs.

Justification Due to the growing incidence of wildfires, temperature increase with climate change and increased urbanization, more people are exposed to high levels of ozone despite standards set by international and national agencies. Despite health warnings, many choose to continue engaging in exercise during high ozone levels. Results from this study will better inform practitioners and exercisers how to engage in exercise during ozone conditions to minimize it's deleterious effects on health.

Research Design This is a double-blinded randomized cross over design with pre- and post-measures. Ozone status (room air and 180 parts per billion (PPB) ozone) and exercise intensity (moderate and heavy) are the independent variables each with two levels. Testing will take place over 5 laboratory visits separated by at least 7 days. During the first session, subjects will undergo body plethysmography, spirometry, and a Step-ramp-step test on a cycle ergometer to determine subject characteristics and exercise thresholds. During visits 2-5, participants will be randomized to 1 of 4 exercise conditions manipulating exercise intensity and ozone status. They will then be asked to exercise for a duration that incurs the same effective dose of ozone across conditions with ozone exposure. If the participant is exercising in a non-ozone condition, they will be asked to exercise for however long it would take to incur the same effective dose had they been exposed to 180 ppb of ozone during the exercise bout. During the exercise bout, participants will be asked to rate their subjective symptoms associated with ozone exposure, dyspnea, and RPE every 15 minutes. Once the exercise bout is complete, participants will immediately perform pulmonary function testing and will be asked to rate their subjective symptoms associated with ozone exposure, dyspnea, and RPE.

Statistical Analysis To analyze changes in pulmonary function, dyspnea, and subjective symptoms within exercise conditions a repeated measures ANOVA will be conducted. To analyze changes in these variables across conditions relative to ozone status, exercise intensity, sex, and lung size, a multivariate ANOVA will be conducted. To test for significance within and across conditions, a Tukey test will be performed. All data analysis will be conducted in R. The sample size employed for the study will be 18 (n = 9 male, n =9 female)

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Currently training and/or competing in endurance sport
  2. Maximal oxygen consumption (VO2max) greater than 60 ml/kg/min (males) or 50 ml/kg/min (females)
  3. Between the ages of 18 and 50
  4. Able to communicate sufficiently using the English language
  5. Taking hormonal birth control (female participants only)

Exclusion criteria

  1. History of smoking
  2. Upper respiratory tract infection within the last 4 weeks
  3. EIB, Asthma
  4. Presence of any chronic respiratory disease
  5. Current symptoms of, or current infection with COVID-19
  6. Pregnant or suspected pregnancy

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

0 participants in 4 patient groups

Ozone, High Intensity
Experimental group
Description:
Participants will exercise for 45 minutes in the heavy intensity domain while exposed to 180 ppb ozone
Treatment:
Other: Ozone
Behavioral: Heavy Intensity
Ozone, Moderate Intensity
Experimental group
Description:
Participants will exercise for 75 minutes in the moderate intensity domain while exposed to 180 ppb ozone
Treatment:
Behavioral: Moderate Intensity
Other: Ozone
Filtered Air, Heavy Intensity
Sham Comparator group
Description:
Participants will exercise for 45 minutes in the heavy intensity domain while exposed to filtered air.
Treatment:
Other: Filtered Air
Behavioral: Heavy Intensity
Filtered Air, Moderate Intensity
Sham Comparator group
Description:
Participants will exercise for 75 minutes in the moderate intensity domain while exposed to filtered air
Treatment:
Behavioral: Moderate Intensity
Other: Filtered Air

Trial contacts and locations

1

Loading...

Central trial contact

Matthew G Skirrow, BSc

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems