Sleep Clinical Trial
Official title:
Effect of Sleep Timing, Independent of Duration, on Food Intake and Metabolic Control of Energy Balance
The purpose of this study is to test the effects of sleep and meal timing, independent of
sleep duration, on glucose regulation and metabolic and hormonal control of energy balance
in normal weight adults.
This study will be a 4-phase, randomized controlled study of 5 days each in which
participants will undergo 2 phases of late sleep times that differ in meal timing (normal or
late) and 2 phases of normal sleep times that differ in meal timing (normal or late).
The Aims and Hypotheses of this study are:
Aim 1: To compare hormonal regulation of food intake and metabolic risk markers in response
to altered sleep and meal timing.
- Hypothesis 1: There will be an interaction between sleep and meal time on glucose,
insulin, and glucose and insulin area under the curve after the glucose tolerance test
such that the late sleep/late meal will result in the worst metabolic profile, normal
sleep/late meal and late sleep/normal meal will have an intermediate profile, and
normal sleep/normal meal will result in the best metabolic profile.
- Hypothesis 2: There will be an interaction between sleep and meal time on leptin and
ghrelin concentrations such that the late sleep/late meal timing phase will result in
low leptin/high ghrelin, normal sleep/late meal timing and late sleep/normal meal will
have an intermediate profile, and normal sleep/normal meal timing will result in high
leptin/low ghrelin.
Aim 2: To compare food intake over a 24-h period in response to altered sleep and meal
timing.
• Hypothesis 3: Energy and fat intakes will be greater during the late sleep timing phase
compared to normal sleep timing.
Status | Completed |
Enrollment | 5 |
Est. completion date | September 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 20 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Body mass index 22-25 - Normal scores on sleep questionnaires (PSQI, ESS, Berlin, SDIQ) - Normal score on Beck Depression Inventory - Intermediate chronotype on Composite Scale of Morningness/Eveningness Exclusion Criteria: - Neurological, medical, or psychiatric disorders - Eating disorders - Diabetes - Sleep disorders - Travel across time zones - History of drug/alcohol abuse - Caffeine intake >300 mg/d - Excessive daytime sleepiness - Pregnancy or within 1 y post-partum |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | St. Luke's/Roosevelt Hospital | New York | New York |
Lead Sponsor | Collaborator |
---|---|
St. Luke's-Roosevelt Hospital Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Food intake | Ad libitum food intake will be assessed on day 5 | Single day | No |
Primary | Oral Glucose Tolerance | Oral glucose tolerance test will be performed at scheduled breakfast time on day 4 | 2 hours | Yes |
Primary | Meal tolerance test | Glucose and insulin responses to a liquid meal will be assessed at scheduled lunch time | 3 hours | No |
Secondary | Hormonal profile | On day 3, the following hormones will be assessed from overnight hours: glucose, insulin, cortisol, melatonin, leptin, ghrelin, PYY, GLP-1 | 24 hours | No |
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