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Sleep Loss and Energy Metabolism in People With Family History of Type 2 Diabetes.

Sleep, Energy Metabolism and Diabetes Risk.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00724087
Enrollment
12
Registered
2008-07-29
Start date
2008-07-31
Completion date
2012-03-31
Last updated
2013-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insulin Resistance, Sleep, Sleep Deprivation, Type 2 Diabetes

Keywords

short sleep duration, energy expenditure, insulin secretion, insulin action, lipid turnover, free fatty acids

Brief summary

The use of energy from food changes when people sleep. However, it is still not known if differences in the amount of nighttime sleep have an effect on the amount of energy that people who have a relative with type 2 diabetes (parent, sibling, or grandparent) use to perform their daily activities. This study is being done to test the hypothesis that the daily use of energy in people who have a history of type 2 diabetes in their family will be different after they have slept short hours for 16 days in comparison to when they have slept longer hours for 16 days.

Detailed description

Study participants will complete two 16-day inpatient stays in the sleep laboratory of the University of Chicago Clinical Resource Center that will be scheduled at least 4 weeks apart. Bedtime duration will be set at 5.5 hours per night during one of these stays and at 8.5 hours per night during the other. No daytime naps will be allowed. Study participants will be served regular daily meals including breakfast, lunch, dinner, and a bedtime snack. On weekdays all participants will engage in simulated office work in the sleep laboratory. During the rest of the time participants will maintain their usual indoor and outdoor activities as much as possible within the limits of the University of Chicago campus. At the beginning of each inpatient stay, study participants will 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 and again 14 days later in order to measure the amount of energy that was used by them during this time. At the end of each stay participants will also undergo measurements of their body composition (lean tissue, bone and fat) and their metabolic rate at rest and after a standard meal, and will complete tests to determine how much insulin does their body produce in response to an intravenous glucose infusion and how effective is the action of the sugar-processing hormone, insulin, in their body when it is infused intravenously together with glucose over a period of several hours.

Interventions

OTHER5.5-hour bedtime

16 days with sleep allowed only during a 5.5-hour bedtime period at night

OTHER8.5-hour bedtime

16 days with sleep allowed only during a 8.5-hour bedtime period at night

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Chicago
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* regular sleep habits * BMI 20 to 27 kg/m2 * at least one parent, sibling or grandparent with type 2 diabetes * must exercise regularly

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 * women only: use of birth control pills * women only: irregular menstrual periods or pregnancy * use of medications/compounds that can disrupt sleep

Design outcomes

Primary

MeasureTime frame
Total energy expenditureduring each bedtime intervention

Secondary

MeasureTime frame
Physical activity related energy expenditureduring each bedtime intervention
Total body insulin sensitivityat the end of each bedtime intervention
First and second phase insulin secretionat the end of each bedtime intervention
Endogenous glucose productionat the end of each bedtime intervention
Glycerol turnover and free fatty acid concentrationat the end of each bedtime intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026