Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID06679543

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

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Baseline Assessment

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)

Testing Visits

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

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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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