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NCT05713370Completed

Sleep Restriction and Postprandial Lipemia

Source: ClinicalTrials.gov · Last updated 31 Jan 2024

Brief summary (registry, in English)

Sleep restriction increases overnight and early morning non-esterified fatty acids (NEFA) levels, which are correlated with whole-body decreases in insulin sensitivity, consistent with the observed impairment of intracellular insulin signaling. Adipose tissue biopsies from sleep restricted subjects that are insulin stimulated have reduced phosphorylation of protein kinase B (pAKT). This protein is involved in suppression of intracellular lipolysis and NEFA release. Aerobic exercise has beneficial effects on postprandial lipemia and insulinemia in normal-weight and obese individuals. Acute moderate-intensity aerobic exercise (30-90 min) performed 12-18 h before an oral fat tolerance test or mixed meal test reduces postprandial triglycerides (TG) and insulin concentrations. This response is largely dependent upon the exercise-induced energy deficit as the response is abolished when the calories expended during exercise are replaced. However, it is not known if sleep restriction will interfere with the beneficial effects of prior exercise on postprandial lipemia. The aim of this project is to investigate if sleep restriction negates the positive effect that exercise has on postprandial lipemia. It is hypothesized that sleep restriction will negate the beneficial effects of prior exercise on postprandial lipemia. Additionally sleep restriction will result in a worsening of the lipid profile compared to no exercise. For the proposed study, the investigators will use a repeated measures analysis of variance (ANOVA) (4 study conditions (no exercise+ sleep restriction, no exercise+normal sleep, exercise+normal sleep, exercise+sleep restriction) x time will be used to analyze changes in NEFA and TG concentrations while a one way ANOVA will be used to analyze area under the curve of the NEFA and TG concentrations.

Status (registry)
Completed
Study type
Interventional
Enrollment
10 (actual)
First submitted
13 Jan 2023
Start date
1 Jul 2022
Primary completion date
1 Dec 2023
Lead sponsor
University of Missouri-Columbia
Diseases
Obesity
NCT number
NCT05713370

What you commit to

  • Study type: Interventional
  • Participants enrolled: 10
  • From 1 Jul 2022 to the primary completion date, 1 Dec 2023
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • taking lipid-lowering medications
  • any medications known to impact metabolism, appetite, or sleep

Other illness

  • diagnosed with cardiovascular disease
  • any allergies to milk, ice cream, peanut butter and soy.

Other

  • type 2 diabetic
  • hypertensive
  • smokers
  • pregnant
  • sleep apnea
  • fragmented sleep
  • have any recent changes in hormonal birth control
  • night shift workers or take regular daytime naps

Who the study is looking for

  • Overweight and obese men and women
  • 21-45 years of age
  • BMI of 25-35 kg/m2
  • Normal sleeping habits of 7-9 hours per night

Age in the registry: 21 years to 45 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Missouri
Coordinator of this site? Confirm its status
ColumbiaUnited StatesUnknown status
University of Misouri
Coordinator of this site? Confirm its status
ColumbiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.