Study Summary
This trial looks at whether men and women respond differently to a type of exercise called sprint interval training.
Treatment Effectiveness
Effectiveness Progress
Study Objectives
1 Primary · 3 Secondary · Reporting Duration: Change from baseline after 4 and 12 weeks of sprint interval exercise training
Week 12
Peak cardiac output
Peak oxygen uptake
Week 12
Flow mediated dilation
Pulse wave velocity
Trial Safety
Safety Progress
Trial Design
2 Treatment Groups
Males
1 of 2
Females
1 of 2
Experimental Treatment
20 Total Participants · 2 Treatment Groups
Primary Treatment: Sprint interval exercise training · No Placebo Group · N/A
Males
Other
Experimental Group · 1 Intervention: Sprint interval exercise training · Intervention Types: OtherFemales
Other
Experimental Group · 1 Intervention: Sprint interval exercise training · Intervention Types: OtherTrial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: change from baseline after 4 and 12 weeks of sprint interval exercise training
Who is running the clinical trial?
McMaster UniversityLead Sponsor
801 Previous Clinical Trials
1,727,837 Total Patients Enrolled
5 Trials studying Exercise
126 Patients Enrolled for Exercise
Martin Gibala, PhDPrincipal InvestigatorMcMaster University
2 Previous Clinical Trials
60 Total Patients Enrolled
2 Trials studying Exercise
60 Patients Enrolled for Exercise
Eligibility Criteria
Age 18 - 35 · All Participants · 3 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:You are female and are naturally cycling or are using a 2nd generation oral contraceptive.
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Conditions
Cancer Related
Treatments