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Recruiting NCT07329283

NCT07329283 Nighttime Synchrony of Your Nutrition and Circadian Health

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Clinical Trial Summary
NCT ID NCT07329283
Status Recruiting
Phase
Sponsor University of Utah
Condition Sleep
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2025-12-19
Primary Completion 2030-05-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 35 Years
Study Type INTERVENTIONAL
Interventions
Central Clock MisalignmentPeripheral Misalignment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2025-12-19 with a primary completion date of 2030-05-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

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.

Contact & Investigator

Central Contact

Victoria Miranda, MS

✉ SleepStudyParticipant@utah.edu

📞 385-309-0551

Principal Investigator

Christopher Depner, PhD

PRINCIPAL INVESTIGATOR

University of Utah

Frequently Asked Questions

Who can join the NCT07329283 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 35 Years, studying Sleep. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07329283 currently recruiting?

Yes, NCT07329283 is actively recruiting participants. Contact the research team at SleepStudyParticipant@utah.edu for enrollment information.

Where is the NCT07329283 trial being conducted?

This trial is being conducted at Salt Lake City, United States.

Who is sponsoring the NCT07329283 clinical trial?

NCT07329283 is sponsored by University of Utah. The principal investigator is Christopher Depner, PhD at University of Utah. The trial plans to enroll 120 participants.

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