Actively Recruiting
Effects of Partial Sleep Deprivation on Cardiac Output During Cycling Exercise in Healthy Adults
Led by University of Guelph · Updated on 2026-04-28
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to understand how partial sleep deprivation affects cardiac output and blood pressure during cycling exercise in young healthy adults, with about half of the participants being female. The study particularly focuses on whether decreases in plasma volume lead to lower cardiac output and blood pressure, and investigates differences between males and females. The trial builds on previous findings that males show reduced systolic blood pressure after partial sleep deprivation while females do not. Participants will take part in three visits. The first visit measures maximal oxygen uptake to assess aerobic fitness and determine exercise intensity zones. The next two visits involve randomized testing after either a normal night of sleep or a night with approximately 40% reduced sleep (partial sleep deprivation). During these visits, participants will perform a 60-minute cycling exercise while researchers measure blood pressure, stroke volume, cardiac output, and plasma volume. Blood samples will be collected through intravenous lines before, during, and after exercise. Participants will keep daily diaries of their sleep and food and beverage intake. Sleep will be monitored for one week before each testing visit using questionnaires and wrist actigraphy. Throughout the study, researchers will assess the cardiac output response to cycling exercise as the primary outcome, along with secondary outcomes including blood pressure and plasma volume responses. The study will last about three weeks, with safety monitoring and adherence to sleep protocols throughout the process.
CONDITIONS
Brief Title
Effects of Partial Sleep Deprivation on Cardiac Output During Cycling
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Free of known cardiovascular or metabolic diseases or sleep disorders
- No history of smoking within the past 3 months
- Able to engage in physical activity as assessed by the physical activity readiness questionnaire (PAR-Q+)
- No prescription of chronic medications other than oral contraceptives
- Able to follow sleep protocols for all visits
- Not allergic to ultrasound gel
- Not pregnant
You will not qualify if you...
- Diagnosed with cardiovascular or metabolic disease or sleep disorders
- History of smoking within the past 3 months
- Not ready to engage in physical activity as assessed by the PAR-Q+
- Prescribed chronic medications other than oral contraceptives
- Unable to follow sleep protocols for any testing visit
- Allergic to ultrasound gel
- Pregnant
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo an initial visit to assess maximal oxygen uptake to determine aerobic fitness and metabolic exercise intensity zones.
1 visit (in-person)
Duration - Approximately 3 weeks
Participants complete two randomized testing visits after nights of normal sleep and partial sleep deprivation. Each visit includes a 60-minute cycling exercise with measurements of hemodynamics and plasma volume before, during, and after exercise, along with venous blood sample collection.
2 visits (in-person)
Trial Site Locations
Total: 1 location
1
University of Guelph
Guelph, Ontario, Canada, N1G 2W1
Actively Recruiting
Research Team
J
Julian Bommarito, MSc
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
OTHER
Number of Arms
2
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