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Clinical Trials in Canada / NCT06679543
Recruiting Not applicable

Effects of Partial Sleep Deprivation on Cardiac Output During Cycling

NCT06679543 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-01-02
Last updated
2026-04-28

Condition(s) studied

Sleep Deprivation

Investigational drug(s) / intervention(s)

Partial sleep deprivation

Partial sleep deprivation: Participants will be asked to come to the lab for testing after a night of partial sleep deprivation. Participants will be asked to fall asleep at their habitual bedtime but wake up early (\~40% of normal sleep duration).

Study summary

The goal of this clinical trial is to determine if attenuations in cardiac output drive the blunted blood pressure response during cycling exercise following a night of partial sleep deprivation in young healthy adults (%50 females). The secondary outcome is to assess sex differences. The main questions it aims to answer are:

* Do reductions in plasma volume drive reductions in cardiac output and therefore blood pressure during exercise following a night of partial sleep deprivation?
* Do sex differences exist?

Participants will:

* Visit the lab after a night of normal sleep and a night of partial sleep deprivation.
* Keep a daily diary of their sleep and food/beverage intake.
* Perform maximal and submaximal exercise on a cycle ergometer.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * 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 assessed through the physical activity readiness questionnaire (PAR-Q+) * No prescription of chronic medications other than oral contraceptives * Able to abide by sleep protocols for all visits * Individuals who are not allergic to ultrasound gel * Individuals who are not pregnant Exclusion Criteria: * Individuals diagnosed with cardiovascular or metabolic disease or sleep disorders * Has a history of smoking (within the past 3 months) * Not ready to engage in physical activity as assessed by the PAR-Q+ * Individuals prescribed chronic medications other than oral contraceptives * Unable to abide by sleep protocols for any testing visit * Allergic to ultrasound gel * Pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Guelph Guelph Ontario Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06679543 on ClinicalTrials.gov ↗ ← All trials in Canada