Short Sleepers' gut bugs under the microscope
NCT ID NCT07567560
First seen Jun 24, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This study looks at the gut bacteria of natural short sleepers—people who sleep less than 6 hours a night but feel fine. Researchers want to see if these individuals have a unique mix of gut microbes compared to others. The goal is to understand how sleep affects gut health, which could lead to better health tips for people with poor sleep.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could reveal how gut bacteria differ in people who naturally sleep less, possibly pointing to ways to improve health for those with poor sleep.
- What could go wrong
- This is a small, early observational study with only 34 participants, so findings may not apply to everyone. It does not test any treatment, so direct health benefits are not expected.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 34 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Natural Short Sleepers are defined as individuals who sleep between 4 and 5.5 hours per night without any impact on health or daytime mental fatigue levels.
- Ages
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20 to 50 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion: 1. Men between 20 - 50 years of age and pre-menopausal women between 20 - 45 years of age (inclusive). 2. Consistent schedule during daytime hours. 3. Body Mass Index (BMI) 18.5 - 35 kg/m2 (inclusive). 4. Good physical and mental health as established by self-reported medical history and evaluated by a study investigator. 5. Willingness to maintain and record their general habits, eating, and daily activity/exercise pattern for the study period. 6. Willingness to maintain typical sleep hygiene patterns (e.g. sleep location, temperature, environment). 7. Willingness to maintain their current pattern of alcohol consumption for the duration of the study. 8. Willing and able to participate fully in all aspects of the study and complete all study procedures, including providing signed informed consent. 9. Willing and able to attend two in-person visits at a trial site 10. Completes all required procedures (screening questionnaire and ePROs) during the 14-day screening period 10a. Two instances of the sleep diary and Karolinska Sleepiness Scale may be missed by the participant without impacting eligibility 11. Has regular bowel habits, on at least 5 days a week. 12. Pittsburgh Sleep Quality Index (PSQI) global score of ≤7 and a sleep efficiency score of ≥80%, self-reported during the screening period. Additionally, no more than one score of 3 is permitted across Question 5 sub-items, and no score of 3 is permitted in Question 10 sub-items, if a bed partner is present 13. Sleep, on average, 4-5.5 hours per night, verified via participant self-report during the screening period. If the participant's average is within the 4-5.5 hour range but slept more than 5.5 hours on any of the nights their eligibility will be assessed per PI/Sponsor discretion. Note: Oura ring data from the run-in period will be reviewed to confirm eligibility based on PI/Sponsor discretion. 14. Report feeling refreshed with no desire to nap during the daytime, with a score of ≤4 on the Epworth Sleepiness Scale (ESS) evaluated during the screening period. 15. Average KSS Score of 1-3 during the screening period. Exclusion: 1. Ever diagnosed with or self-reports a sleep disorder, including sleep apnea, habitual snoring (defined as loud, persistent snoring 3 or more nights per week), insomnia, narcolepsy, or parasomnias. 2. Extreme chronotypes, those who regularly go to sleep prior to 8:00pm. 3. Any current diagnosed or self-reported gastrointestinal disorder, including Crohn's disease, ulcerative colitis, celiac disease, IBS, or functional bowel disorder or chronic heartburn. 4. Regularly wakes up during the night 5 or more times per night for a cumulative amount of 30 minutes as observed via self-report during the screening period, per PI discretion. 5. Currently taking medications (including over-the-counter medications) or dietary supplements that, in the investigator's opinion, may affect the participants' microbiome or sleep. 6. Have taken in the last 3 months medications (including over-the-counter medications) or dietary supplements that, in the investigator's opinion, may affect the participants' microbiome or sleep. 7. Neurodegenerative diseases (including multiple sclerosis, Parkinson's disease, Alzheimer's disease, dementia). 8. Recent history (past year) of alcohol abuse or dependence. Defined as regularly drinking more than 12 drinks for females and more than 20 drinks for males per week and based on PI discretion. 9. Drug abuse or dependence, including consistent recreational substance use such as marijuana. 10. Binge drinking behavior, defined as 4 or more alcoholic drinks for women or 5 or more alcoholic drinks for men in one sitting on 2 or more occasions, within the past 1 month with final decision per PI discretion. 11. Recent history (current use or within the past 1 month) of smoking, vaping or other use of nicotine-containing products. 12. Diagnosed neuropsychiatric disorders or symptoms possibly affecting sleep e.g. (generalized anxiety disorder (GAD), major depressive disorder (MDD), bipolar disorder, schizophrenia) 13. Any use of systemic antibiotics in the past 3 months. This does not include topical or targeted antibiotic use (ointment, spray, eye drop, ear drop). 14. Any use of probiotic supplements in the past 2 weeks. 15. Any use of proton pump inhibitors (PPIs) in the past 2 weeks. 16. Any use of laxatives or antidiarrheals in the past 4 weeks. 17. Any use of non-steroidal anti-inflammatory drugs (NSAIDs) for 5 or more consecutive days in the past 4 weeks. 18. Pregnant or breastfeeding or planning to become pregnant. 19. Personal circumstances affecting stress or sleep (e.g. serving as a caretaker/required to wake up during sleep/major change in personal life). Note: Life situations causing stress or challenges in sleep that are considered shortterm, per PI discretion, may be considered for re-screening 4 weeks after the life situation has resolved, meaning it is no longer causing stress or challenges in sleep. 20. Planned overnight travel during the study. 21. Females experiencing perimenopausal or menopausal symptoms, or those who have been diagnosed as perimenopausal or menopausal by a physician. 22. Any diagnosed condition or undiagnosed symptom which disrupts sleep, including, but not limited to, hyperthyroidism, night sweats, restless legs, or poorly controlled allergic rhinitis. 23. Varying work schedule and/or shift workers who work overnight shifts (e.g. 3rd shift, working late night to early morning hours). 24. Any other personal or medical condition that the investigator believes may bias or confound the results.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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AccuMed
RECRUITINGGarden City, New York, 11530, United States
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Global Life Research Network
RECRUITINGMiami, Florida, 33155, United States
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Lindus Health
RECRUITINGBoston, Massachusetts, 02111, United States
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New Dawn Wellness and Medical Research Center
RECRUITINGHouston, Texas, 77082, United States
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