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Physiologic Effects of Sleep Restriction

Not Applicable
Completed
Conditions
Sleep Deprivation
Interventions
Behavioral: sleep restriction
Registration Number
NCT01433315
Lead Sponsor
Mayo Clinic
Brief Summary

Evidence suggests a relationship between sleep deprivation and cardiovascular disease. The investigators wish to determine whether 9 nights of modest sleep restriction results in activation of cardiovascular disease mechanisms, thus potentially increasing the risk of cardiovascular disease. The investigators hypothesize that sleep restriction will result in elevated blood pressure, inflammation, and neurocognitive deficits.

Detailed Description

Evidence suggests a relationship between sleep deprivation and cardiovascular disease. Voluntary sleep restriction is common, with 28% of the US adult population reports getting 6 or fewer hours of sleep per night, and those who do are 24% more likely to have cardiovascular disease and have twice the risk of hypertension. Insufficient sleep may conceivably be one of the most common, and most preventable, cardiovascular risk factors. The investigators wish to determine whether 9 nights of modest sleep restriction results in activation of cardiovascular disease mechanisms, thus potentially increasing the risk of cardiovascular disease. The investigators will combine our cardiovascular studies with state-of-the art sleep monitoring and neurocognitive tests to provide unambiguous data on the physiologic effects of sleep restriction. Together, the investigators findings will help explain whether the reduced sleep duration in the general population may be contributing to the current epidemic of cardiovascular disease, and suggest strategies to reduce this risk.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
26
Inclusion Criteria
  • Age 18-40 years
  • No chronic medical conditions other than seasonal or environmental allergies
  • On no prescription medications other than second generation antihistamines (Cetirizine, Fexofenadine, Desloratadine, Loratadine, etc), oral contraceptive pills, or intrauterine devices.
  • BMI 18.5-35 kg/m2
  • Both normotensive and prehypertensive people are eligible and will be studied
  • Not a current smoker or tobacco user
  • Not pregnant or breast feeding and not intending to become pregnant or breast feed
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Exclusion Criteria
  • The investigators will exclude subjects who have any medical or psychiatric disorders
  • History of anxiety or depression, and those taking any medications other than non-sedating antihistamines or oral contraceptives.
  • Those found to have depression on a depression screening tool (BDI-II) will be excluded. Current smokers will be excluded.
  • All female subjects will undergoing a screening pregnancy test and excluded if positive.
  • Subjects found to have significant sleep disorders will be excluded.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
sleep restrictionsleep restrictionrestricted sleep during the experimental period
Primary Outcome Measures
NameTimeMethod
Change in blood pressurethroughout 16 days

Change in mean arterial blood pressure over 24 hours, measured during acclimation, experimental, and recovery timepoints over the study period.

Secondary Outcome Measures
NameTimeMethod
Change in electrocardiographic characteristicsthroughout 16 days

Change in electrocardiographic characteristics, measured during acclimation, experimental, and recovery timepoints.

Change in fat tissue characteristicsthroughout 16 days

Change in fat tissue characteristics, determined by analysis of a fat biopsy sample.

Change in catecholaminesthroughout 16 days

Change in catecholamines, measured during acclimation, experimental, and recovery

Change in arterial stiffnessthroughout 16 days

Change in arterial stiffness, measured during acclimation, experimental, and recovery timepoints.

Change in markers of inflammationthroughout 16 days

Change in markers of inflammation, measured during acclimation, experimental, and recovery timepoints.

Change in baroreflex sensitivitythroughout 16 days

Change in baroreflex sensitivity, measured during acclimation, experimental, and recovery

Change in endothelial functionthroughout 16 days

Change in endothelial function, measured during acclimation, experimental, and recovery timepoints.

Trial Locations

Locations (1)

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

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