Skip to main content
Clinical Trials/NCT00721084
NCT00721084
Completed
Not Applicable

Sleep, Energy Metabolism and Diabetes Risk

University of Chicago1 site in 1 country30 target enrollmentJuly 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep
Sponsor
University of Chicago
Enrollment
30
Locations
1
Primary Endpoint
Total energy expenditure
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Currently, it is not known if the amount of nighttime sleep has any effect on the overall physical fitness, and on how much energy do people who have a relative with type 2 diabetes (parent, sibling, or grandparent) use to perform activities of daily living. This study will test the hypothesis that individual differences in nighttime sleep duration are related to differences in the amount of energy used to perform activities of daily living and the overall level of physical fitness of the individual.

Detailed Description

The study includes 2 weeks of monitoring of the participants' patterns of sleep and wakefulness at home. At the beginning of this period, all participants will undergo measurements of their body composition (lean tissue, bone and fat) and their metabolic rate at rest and after a standard meal. At that time, all participants will also drink a glass of water containing harmless non-radioactive dense forms of oxygen and hydrogen, small amounts of which are found in natural water. Several urine samples will be collected before and after the participants drink the water at the beginning of the study and again 14 days later in order to measure the amount of energy that was used by them during this time. Participants will also wear small wristwatch-like activity monitors on their wrist and around their waist as they follow their usual everyday activities and sleep-wake schedules at home. The recordings from these monitors combined with daily sleep logs will be used to determine when the participants slept and when they were awake. On the last day of the study, the participants will undergo MRI measurements of the distribution of fat in their abdomen and complete a graded exercise test on a treadmill or stationary bicycle in order to determine what is the most strenuous level of exercise that they can perform. A medical doctor will supervise all study procedures that are done in the research laboratory.

Registry
clinicaltrials.gov
Start Date
July 2008
End Date
March 2012
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • regular sleep habits
  • BMI 20 to 27 kg/m2
  • at least one parent, sibling or grandparent with type 2 diabetes
  • no regular exercise habits

Exclusion Criteria

  • active smoker
  • night or shift work
  • have highly variable sleep habits
  • have a hormonal disorder
  • have a sleep disorder
  • have an active medical problem
  • for women: use of birth control pills
  • for women: irregular menstrual periods or pregnancy
  • use of medications/compounds that can disrupt sleep

Outcomes

Primary Outcomes

Total energy expenditure

Time Frame: during a 2-week observation period

Secondary Outcomes

  • Amount and distribution of body fat(at the end of the observation period)
  • Physical activity related energy expenditure(during a 2-week observation period)
  • Maximal aerobic capacity(at the end of the observation period)

Study Sites (1)

Loading locations...

Similar Trials