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NCT07329283 · University of Utah

Nighttime Synchrony of Your Nutrition and Circadian Health

(N-Sync)

What this study is about

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.

View original scientific description

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.

Interventions

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.

BEHAVIORAL

Peripheral Misalignment

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

Primary outcome measures

Insulin Sensitivity

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

Insulin sensitivity will be measured by intravenous glucose tolerance tests.

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.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

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
  • 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.

Where

  • Salt Lake City, Utah

Related conditions & keywords

SleepMetabolism ChangesCircadian RhythmLifestyle FactorsSleep HygieneSleep Hygiene, InadequateSleep DeprivationInsufficient SleepCircadian MisalignmentCircadian DysregulationLight ExposureMetabolismFood Intake

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Jan 22, 2026 · Source of record for eligibility and locations

📊
1 of 120 participants interested
1% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Salt Lake City

Utah

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Sleep Treatment in Salt Lake City?

Join others in Utah exploring innovative treatment options through clinical research

Sleep Treatment Options in Salt Lake City, Utah

If you're searching for Sleep treatment in Salt Lake City, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Salt Lake City and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Sleep. All study-related care is provided at no cost to participants.

Local Sites
1 locations in Utah
Now Enrolling
Up to 120 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Sleep?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Sleep

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Sleep Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07329283. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.