How a Western versus a fiber-rich diet affects sleep and daily body rhythms
Official title: Inverkan av Kost pa Dygnsrytmer Och Amnesomsattning
Run by Uppsala University · NCT07138313 · Data updated 2026-11-12
It will test whether eating a Western-style unhealthy diet versus a healthier, fiber-rich diet changes sleep quality and daily heart, glucose, and hormone rhythms in healthy young adults.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 32 Years |
| Sex | All |
| Enrollment | 24 (estimated) |
| Sponsor | Uppsala University Academic / other |
| Locations | 1 site (Uppsala) |
| Status | Recruiting |
| Started | September 22, 2025 |
| Main results expected | July 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | February 4, 2026 |
| Trial ID | NCT07138313 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Healthy non-smoking adults aged 18–32 with BMI 18–27 kg/m2, stable weight, regular sleep (7–9.25 hours nightly), regular exercise, and three daily meals are the intended participants.
✕Probably not a fit
People with chronic medical or psychiatric conditions, diagnosed sleep disorders, recent shift work, smokers, those on chronic medications, or those outside the specified age/BMI ranges are unlikely to gain personal health benefits from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a randomized crossover experiment where each participant follows two different diets (Western-style high-fat versus a healthier, fiber-rich diet) with about a week of at-home monitoring followed by a multi-day stay in the lab under controlled conditions. Sleep will be measured objectively with polysomnography and with wearable devices, while continuous glucose monitoring, heart rate, and blood pressure will capture 24-hour physiological patterns. Repeated biological sampling across the day will measure hormonal, cardiometabolic, neurodegenerative, and gut microbial biomarkers, and cognitive performance, mood, and appetite will also be recorded. Comparing the same people on both diets will help isolate direct diet-driven changes in sleep and related physiology.
Why it matters
Potential benefit: If successful, the results could point to straightforward dietary changes that improve sleep and daily metabolic rhythms and potentially reduce long-term cardiometabolic or neurodegenerative risk.
How similar studies have gone: Observational and some interventional work links diet composition to sleep and metabolism, but detailed randomized crossover trials with continuous 24-hour physiological and multi-compartment biomarker sampling are limited, so this approach is partly novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18-32 yr * Healthy (self-reported) and not on chronic medication * BMI 18-27 kg/m2 (and waist circumference \<102 cm), and weight stable (less than 5% body weight change in the past 6 months) * Non-smoker and non-nicotine user * Regular sleep-wake pattern, with sleep duration of 7-9.25 hrs per night * Regular exercise habits the last 2 months * Regular daily meal pattern with 3 main meals Exclusion Criteria: * Major or chronic illness, e.g. diabetes, renal disease or inflammatory bowel disease * Current or history of endocrine or metabolic disorders * Psychiatric or neurological disorders (e.g. bipolar disorder, epilepsy) * Frequent gastrointestinal symptoms * Chronic medication * Any sleep disorder (including recent or chronic symptoms of insomnia) * Shift work in the preceding three months or for a long duration * Extreme chronotype or physical activity patterns * Time travel over two time zones in the preceding month * Too much weight gain or weight loss in the preceding 6 months (±5% body weight in past 6 months) * Any issues with or allergies against the provided food items * Recent major dietary changes or adoption of specific dietary regimens * Women who are pregnant, breastfeeding, or planning to become pregnant during the study period. * Use of illicit drugs or substances of abuse
Where it's running
-
Uppsala biomedical center
Uppsala, Sweden Recruiting
Study contacts
- Principal investigator: Jonathan Cedernaes, MD, PhD — Uppsala University, Sweden
- Study coordinator: Jonathan Cedernaes, MD, PhD
- Email: jonathan.cedernaes@medsci.uu.se
- Phone: 0184710000
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Sleep and circadian care for ICU patients
This study tests a multicomponent sleep and circadian rhythm program in adult ICU patients to see if it helps keep daily rhythms and sleep better.
-
Overnight Temperature Regulation to Test Gut Health, Inflammation, and Circadian Rhythms
This study tests whether two weeks of using the Eight Sleep Pod at night can improve gut bacteria balance, lower inflammation, and strengthen daily temperature and blood pressure rhythms in postmenopausal women and age-matched men with poor sleep.
-
Morningness vs. eveningness and how quickly healthy adults recover after submaximal exercise
This study tests whether people who prefer morning or evening are linked to how quickly healthy adults recover after a light-to-moderate workout.
-
Morning Bright Light for Better Daytime Functioning in University Students
This study tests whether a one-week, morning 30-minute bright light session improves sleep quality and daytime alertness and mood in healthy university students.
-
Chronotype and time-of-day test of time perception in morning and evening types
This study tests whether matching a person’s chronotype (morning or evening) with the testing time (morning or evening) changes how accurately they perceive time.
-
Tailored Anti-Inflammatory Diet for Crohn's Disease
This study tests a personalized anti-inflammatory diet for people with Crohn’s disease to see if it improves symptoms and inflammation and to find biomarkers of response.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.