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Official title Impact of Intermittent Fasting on Sleep and Quality of Life
ClinicalTrials.gov ID: NCT06959069
What this study is testing
- What it's testing
- The goal of this clinical trial is to investigate the impact of intermittent fasting on sleep, quality of life and fatigue among healthy volunteers. The main questions aim to answer: Whether intermittent fasting would allow participants to experience an improvement in their sleep quality, duration and latency?
- Time commitment: about 10 weeks
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65. Healthy volunteers may be eligible.
You may be able to join if
- Healthy people
- Adult people - age: between 18 and 65 years old
- people with a BMI between 18.5 and 29.9 kg/m\^2
- Male and female people
You likely can't join if
- people \< 18 years old
- people with Diabetes Mellitus (type 1 and type 2)
- Pregnant and/or breastfeeding and/or postpartum women
- Underweight people (BMI \< 18.5)
- Obese people (BMI \> 30)
- people with confirmed sleep disorders (requiring CPAP or sleep medication (sleeping pills))
See the full eligibility criteria
- Healthy people
- Adult people - age: between 18 and 65 years old
- people with a BMI between 18.5 and 29.9 kg/m\^2
- Male and female people
- people \< 18 years old
- people with Diabetes Mellitus (type 1 and type 2)
- Pregnant and/or breastfeeding and/or postpartum women
- Underweight people (BMI \< 18.5)
- Obese people (BMI \> 30)
- people with confirmed sleep disorders (requiring CPAP or sleep medication (sleeping pills))
- people with renal failure (GFR \< 30 ml/min/1.73 m\^2) or liver disorder
- people with serious cardiovascular, respiratory, neurological, or metabolic medical conditions
- people with malignant tumors
- people with a serious mental disorder requiring medication (e.g., antidepressants or anxiolytics)
- people with eating disorders
- people who have undergone major surgery or have been hospitalized due to major medical condition (surgery, stay in intensive care) within the last one year
- people who have lost more than 10% of their body weight within the last one year
- people actively participating in a weight-loss program
- people with alcohol use disorder (maximum 10 standard alcoholic drinks per week, 2 standard alcoholic drinks per day)
- people with substance use disorder
- people unable to provide informed consent
- people who do not participate simultaneously in another clinical trial
The study team makes the final eligibility decision.
Where it's taking place
- Brussels, Belgium
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 10 weeks per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Brussels, Belgium. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.