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NCT Number: NCT07329283

Nighttime Synchrony of Your Nutrition and Circadian Health

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.

Recruiting

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Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

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

[email protected]

8015812275

Christopher Depner, PhD

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Central Clock Misalignment

Behavioral

Light exposure will be dimmed during the first 4 hours of scheduled wakefulness, with bright light exposure during the nighttime hours of extended wakefulness.

Peripheral Misalignment

Behavioral

Most daily calories will be given later in the day to shift eating patterns toward the nighttime hours.

Primary outcomes

  1. Insulin Sensitivity

    Time frame: Immediately following the 5-day sleep restriction segment

    Insulin sensitivity will be measured by intravenous glucose tolerance tests.

  2. Internal Circadian Misalignment (Uridine and Isobutyryl-L-carnitine)

    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.

Other outcomes

  1. Timing of DLMO and DLMOff

    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.

  2. Hunger and Satiety Visual Analog Scales

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Grace Zimmerman, PhD

CONTACT

[email protected]

385-309-0551

Victoria Miranda, MS

CONTACT

[email protected]

385-309-0551

Sponsors and collaborators

Lead sponsor

University of Utah

Other

Registry information

Official study title

Nighttime Synchrony of Your Nutrition and Circadian Health: The N-Sync Study

Acronym: N-Sync

Important dates

Study start
2025
Primary completion
2030
Study completion
2031
First posted
Jan 9, 2026
Registry last updated
Jan 22, 2026

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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