← Back to Search

Behavioural Intervention

High Fat Meal for Sleep Deprivation

N/A
Waitlist Available
Led By Jill Kanaley, PhD
Research Sponsored by University of Missouri-Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 hour
Awards & highlights

Study Summary

This trial seeks to understand if sleep restriction can negate the positive effects of exercise on postprandial lipemia. #SleepLoss & #Exercise effects on lipid profile will be tested. ANOVA will measure changes in NEFA & TG concentrations.

Eligible Conditions
  • Obesity
  • Sleep Deprivation

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 hour
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 hour for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
area under the curve of fatty acids concentrations
area under the curve of triglycerides concentrations
Secondary outcome measures
area under the curve of glucose concentrations

Trial Design

4Treatment groups
Experimental Treatment
Placebo Group
Group I: no exercise, SRExperimental Treatment1 Intervention
75 g of glucose will be given at the beginning of the study day (the evening prior there will be no exercise the night before the study day, 4 h of sleep the previous night)
Group II: Exercise, no SRExperimental Treatment1 Intervention
75 g of glucose will be given at the beginning of the study day (the evening prior there will be 45 min of exercise the night before the study day, normal sleep (8 h))
Group III: Exercise, SRExperimental Treatment1 Intervention
75 g of glucose will be given at the beginning of the study day (the evening prior there will be 45 min of exercise the night before the study day, 4 h of sleep the previous night)
Group IV: no exercise, no SRPlacebo Group1 Intervention
75 g of glucose will be given at the beginning of the study day (the evening prior there will be no exercise the night before the study day, normal sleep (8 h))
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
high fat meal
2022
Completed Phase 1
~70

Find a Location

Who is running the clinical trial?

University of Missouri-ColumbiaLead Sponsor
365 Previous Clinical Trials
628,227 Total Patients Enrolled
20 Trials studying Obesity
2,192 Patients Enrolled for Obesity
Jill Kanaley, PhDPrincipal InvestigatorUniversity of Missouri-Columbia
7 Previous Clinical Trials
299 Total Patients Enrolled
2 Trials studying Obesity
37 Patients Enrolled for Obesity

Media Library

Sleep Restriction (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05713370 — N/A
Obesity Research Study Groups: Exercise, SR, no exercise, no SR, no exercise, SR, Exercise, no SR
Obesity Clinical Trial 2023: Sleep Restriction Highlights & Side Effects. Trial Name: NCT05713370 — N/A
Sleep Restriction (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05713370 — N/A
Obesity Patient Testimony for trial: Trial Name: NCT05713370 — N/A
~3 spots leftby Jun 2025
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Back to top