Actively Recruiting

Phase Not Applicable
Age: 18Years - 32Years
All Genders
Healthy Volunteers
ID07138313

Impact of Diet on Circadian Rhythms and Metabolism Evaluating Low-Fat and High-Fat Dietary Interventions on Sleep and Physiological Functions

Led by Uppsala University · Updated on 2026-02-04

24

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how different diets affect sleep and related body functions such as metabolism, heart activity, and hormone levels. This study compares the effects of a Western-style unhealthy diet with a healthier, fiber-rich diet on both objective and subjective sleep measures, along with various biomarkers linked to heart and metabolic health, brain function, and gut microbiota. The goal is to understand how nutrition influences sleep quality and overall physiological health. The study uses a randomized crossover design where participants follow two diet interventions: a low-fat diet and a high-fat diet. Each diet is followed for about one week in daily life, then participants spend approximately two days in a controlled laboratory setting for detailed measurements. Participants will wear monitoring devices to track sleep, heart rate, blood pressure, and glucose continuously, along with biological sample collections at multiple times of the day to assess changes in metabolism, immune function, and microbial profiles. Participants will undergo sleep studies using polysomnography and wearables, provide repeated biological samples, and complete tests evaluating cognitive function, mood, and appetite. Researchers will measure changes in sleep structure, 24-hour heart rate variability, glucose levels, blood pressure, and various biomarkers over up to nine days on each diet. The study includes detailed safety and health monitoring, with total participation lasting about nine to ten days per diet condition.

CONDITIONS

Brief Title

Dietary Impact on Sleep, Rhythms and Related Physiology

Who Can Participate

Age: 18Years - 32Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-32 years
  • Self-reported healthy and not on chronic medication
  • BMI between 18 and 27 kg/m2 and waist circumference less than 102 cm
  • Weight stable with less than 5% body weight change in past 6 months
  • Non-smoker and non-nicotine user
  • Regular sleep-wake pattern with 7 to 9.25 hours of sleep per night
  • Regular exercise habits in the past 2 months
  • Regular daily meal pattern with three main meals
Not Eligible

You will not qualify if you...

  • Major or chronic illness such as diabetes, kidney disease, or inflammatory bowel disease
  • Current or past endocrine or metabolic disorders
  • Psychiatric or neurological disorders like bipolar disorder or epilepsy
  • Frequent gastrointestinal symptoms
  • Use of chronic medication
  • Any sleep disorder including recent or chronic insomnia symptoms
  • Shift work in the past three months or long-term shift work
  • Extreme chronotype or unusual physical activity patterns
  • Time travel over two time zones in the past month
  • Weight change greater than ±5% in past 6 months
  • Allergies or issues with provided food items
  • Recent major dietary changes or special diet regimens
  • Women who are pregnant, breastfeeding, or planning pregnancy during the study
  • Use of illicit drugs or substances of abuse

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Low-fat Dietary Intervention

Duration - Up to 9-10 days

Participants follow a low-fat diet for approximately 1 week, followed by a multi-day stay under standardized laboratory conditions for detailed measurements.

Approximately 9 days including in-field and in-lab visits

High-fat Dietary Intervention

Duration - Up to 9-10 days

Participants follow a high-fat diet for approximately 1 week, followed by a multi-day stay under standardized laboratory conditions for detailed measurements.

Approximately 9 days including in-field and in-lab visits

Trial Site Locations

Total: 1 location

1

Uppsala biomedical center

Uppsala, Sweden, 75324

Actively Recruiting

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Research Team

J

Jonathan Cedernaes, MD, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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