College of Health Research Complex - University of Utah, Salt Lake City 84112
Salt Lake City, Utah, 84112, United States
Location status: Recruiting
Location contact
Christopher Depner, PhD
CONTACT
Christopher Depner, PhD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07329283
Sleep is an important factor for overall health. This study will see how different light exposure patterns and food intake impact a person's metabolism (how the body breaks down food) when sleeping is reduced.
Participants will attend 6 to 8 in-person visits to the study clinic, including three overnight stays. People will complete surveys and medical tests. The study will last about 4 to 6 months.
Interested in participating?
Request Info18 year–35 year
All sexes
Interventional
Not applicable
Salt Lake City, Utah, 84112, United States
Location status: Recruiting
Christopher Depner, PhD
CONTACT
Christopher Depner, PhD
PRINCIPAL_INVESTIGATOR
This study is a randomized in-lab, cross-over trial. Each participant will complete all three arms in either condition order #1 (A-B-C) or order #2 (A-C-B). Each arm will consist of 5 nights of experimental sleep restriction followed by a constant routine protocol for assessment of 24-h rhythms. Sleep restriction in the three arms will occur under the following conditions: (A-control condition) Sleep Restriction with Central and Peripheral Alignment; (B) Sleep Restriction with Central Clock Misalignment; and (C) Sleep Restriction with Peripheral Misalignment. Prior to enrollment participants will complete a comprehensive medical history and clinical overnight sleep disorders screening. Baseline consists of a ~2-week ambulatory real-world monitoring segment that will occur immediately prior to each in-lab sleep restriction condition. Following the 5 days of sleep restriction in each arm, participants will complete an intravenous glucose tolerance test to analyze insulin sensitivity, prior to completing the constant routine.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Light exposure will be dimmed during the first 4 hours of scheduled wakefulness, with bright light exposure during the nighttime hours of extended wakefulness.
Most daily calories will be given later in the day to shift eating patterns toward the nighttime hours.
Time frame: Immediately following the 5-day sleep restriction segment
Insulin sensitivity will be measured by intravenous glucose tolerance tests.
Time frame: During the constant routine, following the 5-day sleep restriction segment
Phase angle between DLMO and acrophase of uridine and isobutyryl-L-carnitine during constant routine.
Time frame: During the constant routine, following the 5-day sleep restriction segment
The phase angle between dim-light melatonin offset (DLMOff) scheduled waketime using hourly saliva samples collected during a constant routine.
Time frame: During the constant routine, following the 5-day sleep restriction segment
Self-reported ratings of hunger, satiety, and prospective food intake will be quantified by 100mm visual analog scales ranging from 0 to 100. For each scale, 0 represents low hunger, satiety, or prospective food intake, with 100 representing the highest hunger, satiety, or prospective food intake.
Contact information is provided by the study sponsor or research team.
Grace Zimmerman, PhD
CONTACT
Victoria Miranda, MS
CONTACT
University of Utah
Other
Nighttime Synchrony of Your Nutrition and Circadian Health: The N-Sync Study
Acronym: N-Sync
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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