Purpose

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.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 35 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  1. Age: 18-35 years old; equal numbers of men and women 2. Body Mass Index (BMI): 18.5-24.9 kg/m2 3. Sleep Habits: habitual self-reported average total sleep time (TST) 7-9 hours per night for prior 6 months

Exclusion Criteria

  1. Clinically diagnosed sleep disorder or apnea hypopnea index (AHI) ≥5 2. Evidence of significant organ system dysfunction or disease (e.g., heart disease, diabetes) 3. Fasting plasma glucose ≥100 mg/dL 4. Major psychiatric illness (e.g., major depressive disorder) 5. Cancer that has been in remission less than 5 years 6. History of shift-work in prior year 7. Weight change >5% of body weight over prior six months 8. Currently following a weight-loss program 9. Menopause 10. Pregnant/nursing 11. Greater than 5-day variation in menstrual cycle length month-to-month 12. Currently smoking 13. Alcohol intake >14 drinks/week or >3 drinks/day. 14. Use of prescription medications (except oral contraceptives) within one month prior to or during in-lab visits. 15. Consumption of illegal drugs or >500mg per day of caffeine.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover Assignment
Primary Purpose
Basic Science
Masking
Triple (Participant, Investigator, Outcomes Assessor)
Masking Description
Randomization to condition order will be concealed to research staff and participants until the conclusion of the condition "A", which all participants will complete first.

Arm Groups

ArmDescriptionAssigned Intervention
No Intervention
Sleep Restriction with Central and Peripheral Alignment
(Arm "A")-Control condition with central and peripheral aligned circadian rhythms
Experimental
Sleep Restriction with Central Clock Misalignment
(Arm "B")-Misalignment of the central clock by nighttime electrical light exposure and dim-light in morning hours.
  • Behavioral: Central Clock Misalignment
    Light exposure will be dimmed during the first 4 hours of scheduled wakefulness, with bright light exposure during the nighttime hours of extended wakefulness.
Experimental
Sleep Restriction with Peripheral Misalignment
(Arm "C")-Misalignment of peripheral oscillators by shifting the majority of food intake to the nighttime hours.
  • Behavioral: Peripheral Misalignment
    Most daily calories will be given later in the day to shift eating patterns toward the nighttime hours.

Recruiting Locations

College of Health Research Complex - University of Utah, Salt Lake City 84112
Salt Lake City 5780993, Utah 5549030 84112
Contact:
Christopher Depner, PhD
8015812275
sleepstudyparticipant@utah.edu

More Details

NCT ID
NCT07329283
Status
Recruiting
Sponsor
University of Utah

Study Contact

Victoria Miranda, MS
385-309-0551
SleepStudyParticipant@utah.edu

Detailed Description

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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.