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NCT Number: NCT06679543

Effects of Partial Sleep Deprivation on Cardiac Output During Cycling

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.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Guelph

Guelph, Ontario, N1G 2W1, Canada

Location status: Recruiting

Location contact

Julian Bommarito, MSc

CONTACT

[email protected]

9052209829

Julian Bommarito, MSc

SUB_INVESTIGATOR

About this study

The investigators recently published data showing systolic blood pressure is attenuated during cycling exercise in males but not females following acute partial sleep deprivation, compared to a night of normal sleep, despite no differences in power output. The mechanisms responsible for this sex difference remain unknown. The investigators have pilot data that suggests males have a reduction in cardiac output following acute partial sleep deprivation, but females do not. Therefore, the primary purpose of this study is to assess hemodynamics (blood pressure, stroke volume, and cardiac output) and plasma volume during cycling exercise following a night of normal sleep and partial sleep deprivation in otherwise healthy males and females.

Thirty young healthy adults (50% female) will be recruited to undergo three visits. The first visit will assess maximal oxygen uptake to determine aerobic fitness and metabolic exercise intensity zones. The following two testing visits will be randomized and will be completed after a night of normal sleep or acute partial sleep deprivation (early awakening, 40% normal sleep duration). Sleep will be measured 1-week before each visit subjectively (questionnaire) to determine habitual sleep timing and duration and objectively (wrist actigraphy) the night before each testing visit. Each testing visit will require participants to complete a constant load 60-minute bout of cycling. Before, during, and after the exercise protocol, the investigators will measure hemodynamics and plasma volume. Venous blood samples will be collected via intravenous lines.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Partial Sleep Deprivation

Other

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).

Primary outcomes

  1. cardiac output responses to cycling exercise

    Time frame: Comparison between normal sleep and partial sleep deprivation, ~3 weeks

    Cardiac output during exercise after a night of normal sleep and after a night of partial sleep deprivation

Secondary outcomes

  1. Blood pressure responses to cycling exercise

    Time frame: Comparison between normal sleep and partial sleep deprivation, ~3 weeks

    Blood pressure during exercise after a night of normal sleep and after a night of partial sleep deprivation

  2. Plasma volume

    Time frame: Comparison between normal sleep and partial sleep deprivation, ~3 weeks

    Plasma volume after a night of normal sleep and after a night of partial sleep deprivation

Study contacts

Contact information is provided by the study sponsor or research team.

Julian Bommarito, MSc

CONTACT

[email protected]

9052209829

Sponsors and collaborators

Lead sponsor

University of Guelph

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 7, 2024
Registry last updated
Apr 28, 2026

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.

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