University of Guelph
Guelph, Ontario, N1G 2W1, Canada
Location status: Recruiting
NCT Number: NCT06679543
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.
Interested in participating?
Request Info18 year–50 year
All sexes
Interventional
Not applicable
Guelph, Ontario, N1G 2W1, Canada
Location status: Recruiting
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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).
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
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
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
Contact information is provided by the study sponsor or research team.
University of Guelph
Other
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.
Published trials that share one or more normalized conditions with this study.
NCT06075914
Dyssomnias, Mental Disorders
Columbus, Ohio, United States
View Trial DetailsNCT07438912
Behavior, Behavioral Symptoms
Tucson, Arizona, United States
View Trial DetailsNCT05551325
Chronobiology Disorders, Circadian Rhythm Sleep Disorder, Unspecified
New Haven, Connecticut, United States
View Trial DetailsNCT05393830
Behavior, Dyssomnias
Boston, Massachusetts, United States
View Trial Details