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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04535219
Other study ID # IRB201901937
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 11, 2021
Est. completion date August 2, 2022

Study information

Verified date August 2023
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Insufficient sleep is associated with an increased risk for cardiovascular disease. The causal mechanisms are currently unknown, but may include endothelial dysfunction. The purpose of this study is to examine the influence of sex and aging on the effects of total sleep deprivation on vascular function and whether exercise training attenuates these effects.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date August 2, 2022
Est. primary completion date August 2, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion criteria: - Males and females - 20 to 30 and 50 to 60 years of age - Females will be eumenorrheic at enrollment or postmenopausal for at least 1 year - No major clinical disease (e.g., diabetes, cardiovascular, liver or chronic kidney disease) to minimize confounding of vascular measures - Participants will be sedentary (=3x per week of =30 minutes of aerobic exercise/session) or trained (=5x per week of moderate/vigorous aerobic exercise training) Exclusion criteria: - Age <20 or 31 to 49 or >60 years - Body mass index =30 kg/m^2 because obesity may affect vascular function - Use of medication that may affect vascular measures - Hormone replacement therapy or hormonal contraceptives within past year - Use of tobacco products (chewing tobacco, traditional or e-cigarettes) because they may influence vascular function - Being perimenopausal, pregnant or lactating because may influence vascular function - Being a shift worker because habitual sleep deprivation and altered circadian rhythm may influence vascular function. - Not having an "intermediate" chronotype based on the Morningness-Eveningness Questionnaire (MEQ; score <31 or >69) because this would influence the effect of overnight sleep deprivation on vascular function. - Sleep complaints based on the Pittsburgh Sleep Quality Index (PSQI; score >5) because this would influence the effect of overnight sleep deprivation on vascular function.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
60 minutes of moderate-intensity treadmill exercise (70% of maximal heart rate determined from the maximal graded exercise test)
Supervised Total Sleep Deprivation
Laboratory-monitored total sleep deprivation

Locations

Country Name City State
United States University of Florida Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Endothelial function Endothelial function will be determined using brachial artery flow-mediated dilation via high resolution duplex ultrasonography. Reactive hyperemia will be produced by inflating a forearm cuff to ~250 mmHg for 5 minutes followed by rapid deflation. through study completion, an average of 1 month
Primary Microvascular function Microvascular function will be assessed using the forearm blood flow response to submaximal handgrip exercise. Brachial artery blood flow and diameter will be assessed using Doppler ultrasound. through study completion, an average of 1 month
Secondary Central arterial stiffness The SphygmoCor XCEL device will be used to measure carotid to femoral pulse wave velocity. through study completion, an average of 1 month
Secondary Central arterial hemodynamics The SphygmoCor XCEL device will be used to obtain central pulse wave analysis. through study completion, an average of 1 month
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