St. Paul's Hospital
Vancouver, British Columbia, V6Z1Y6, Canada
Location status: Recruiting
Location contact
Alanna Hind, MSc
CONTACT
Jordan A Guenette, PhD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07037511
β2-Agonists, commonly used to treat asthma, have also been used by athletes to enhance performance, leading to their ban by the International Olympic Committee in 1972. Research has shown non-asthmatics receive no benefit from these drugs at therapeutic dosages; however, many elite athletes still use them, and asthmatic athletes often win more Olympic medals. In some non-asthmatics, β2-agonists may improve breathing limitations during high intensity exercise, which may improve performance. Therefore, we aim to examine if there is a select group of non-asthmatic individuals who experience breathing limitations that may receive benefit from β2-agonists.
Interested in participating?
Request Info18 year–55 year
All sexes
Interventional
Not applicable
Vancouver, British Columbia, V6Z1Y6, Canada
Location status: Recruiting
Alanna Hind, MSc
CONTACT
Jordan A Guenette, PhD
PRINCIPAL_INVESTIGATOR
Purpose:
The purpose of this study is to examine the effects of β2-agonists on exercise performance in non-asthmatic male and female endurance athletes.
Hypothesis:
Our primary hypothesis is that ß2-agonists will improve exercise duration to a greater degree in athletes who experience expiratory flow limitation (EFL) compared to those who do not experience EFL. Additionally, female athletes will, on average, experience greater benefits with ß2-agonists due to a greater prevalence of EFL than males.
Justification:
While β2-agonists have historically been used by athletes as an ergogenic aid, systematic reviews indicate their ineffectiveness in improving aerobic performance. Consequently, the World Anti-Doping Agency (WADA) revised regulations to allow controlled use of specific β2-agonists. Despite a lack of evidence supporting their ergogenic benefits, positive tests for supratherapeutic doses of salbutamol among elite athletes, such as cyclist Chris Froome and cross-country skier Martin Johnsrud Sundby, suggests a belief in their performance-enhancing capabilities. Additionally, there is a physiological rationale for some non-asthmatics to benefit from these drugs. For instance, therapeutic doses of β2-agonists can induce bronchodilation, resulting in a ~5% increase in forced expiratory volume in one second (FEV1) in non-asthmatics. While this level of bronchodilation does not meet the diagnostic threshold for asthma, it holds potential for enhancing ventilatory responses in certain athletes. For example, a subset of non-asthmatic athletes who develop EFL during exercise, characterized by the inability to increase expiratory flows despite increases in expiratory effort, may derive greater benefits if the bronchodilation is sufficient to attenuate EFL. Indeed, experimental reduction of EFL via breathing a helium-oxygen gas mixture improves ventilatory responses, gas exchange, and endurance performance in non-asthmatics. We speculate that non-asthmatics experiencing EFL during exercise are likely to benefit more from β2-agonists than those who do not develop EFL.
Statistical Analysis:
The effects of salbutamol vs. placebo on exercise duration in all participants will be compared using a paired t-test. In all cases, a P-value < 0.05 will be considered statistically significant. A total of 64 participants (32 males and 32 females) will be recruited to adequately assess the effects of salbutamol on exercise tolerance, dyspnea, and related physiological variables.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Meter-dose inhaler of salbutamol performed using large-volume spacer
Meter-dose inhaler of placebo performed using large-volume spacer
Time frame: Up to 2 weeks
Exercise duration will be measured during a time to exhaustion cardiopulmonary exercise test on a stationary cycle ergometer or treadmill.
Time frame: Up to 2 weeks
Exercise duration will be measured during a time to exhaustion cardiopulmonary exercise test on a stationary cycle ergometer or treadmill. Sexes will be compared within modality.
Time frame: Up to 2 weeks
Expiratory flow limitation will be assessed by placing the tidal flow-volume loop within the maximal flow-volume loop during incremental cardiopulmonary exercise testing on a stationary cycle ergometer or treadmill.
Time frame: Up to 2 weeks
Dyspnea will be assessed during and after both incremental and time to exhaustion cardiopulmonary exercise testing on a stationary cycle ergometer or treadmill with salbutamol.
Time frame: Up to 2 weeks
Ventilatory responses will be measured continuously throughout both incremental and time to exhaustion cardiopulmonary exercise testing on a stationary cycle ergometer or treadmill using a metabolic cart.
Time frame: Up to 2 weeks
A Eucapnic Voluntary Hyperpnea (EVH) test will be performed to assess airway hyperresponsiveness and classify participants as EVH-positive or EVH-negative. All participants will undergo the same cardiopulmonary exercise testing on a stationary cycle ergometer or a treadmill with salbutamol.
Contact information is provided by the study sponsor or research team.
Jordan A Guenette, PhD
CONTACT
Satvir S Dhillon, MSc
CONTACT
University of British Columbia
Other
Physiological, Sensory and Ergogenic Effects of Salbutamol - Implications for Athletic Screening and β2 Agonist Use in Sport
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05331170
Allergic Rhinitis, Asthma
Galveston, Texas, United States
View Trial DetailsNCT03406351
Asthma, Bronchial Diseases
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT03617718
Asthma, Bronchial Diseases
Indianapolis, Indiana, United States
View Trial DetailsNCT04549636
Asthma, Bronchial Diseases
Hamilton, Ontario, Canada
View Trial Details