Sleep better naturally? new study tests dietary supplements for poor sleepers
NCT ID NCT07369869
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether two dietary supplements can help adults who are poor sleepers improve their sleep quality, thinking skills, and stress levels. Over 28 days, 68 participants will take either an active supplement or a placebo. Researchers will measure sleep efficiency, gut bacteria, and mood to see if the supplements make a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- proprietary dietary supplement (standardized ingredients)
- What this could lead to
- If successful, this could point toward a natural supplement to improve sleep quality and reduce stress without medication.
- What could go wrong
- This is a small early-stage trial with only 68 participants, and the supplements are proprietary, so results may not be generalizable. The effect may be small or no different from placebo.
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 68 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
May 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
25 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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 CRITERIA * Participants must self-assess themselves as being in good health. * Aged 25 to 60 years at the time of randomisation * Fluent in English * Identify as a 'poor sleeper' as defined subjectively (i.e. poor sleep quality, unrefreshing sleep) and a total score of \>5 on the Pittsburgh Sleep Quality Index (PSQI). EXCLUSION CRITERIA * Member of own household currently participating in this trial * Evidence of current or recent sleep disorders (e.g. sleep apnoea, insomnia, circadian rhythm disorders), taking any medication which exerts sedative effects, affects the CNS and/or sleep, or be currently unwell with any illness that affects sleep (i.e. disorders of the CNS). An initial screening for sleep disorders will be conducted using the Sleep Disorders Symptom Checklist-25 (SDS-CL; Klingman et al., 2017). If a participant reports positively to any of the 25 questions in terms of being affected for three nights per week, or more, this will be followed up using a clinical interview according to the International Classification of Sleep Disorders (ICSD-3) to exclude on the basis of a sleep disorder * History of seizures or epilepsy * Shift working or have a history of shift work within the previous six months * Currently, or within the previous 8 weeks, consuming any nutritional supplements. * Participation in any other intervention research trials * Sleeping at a location other than their usual residence more than two nights per week during participation * Travel across multiple time zones within the last three months or have planned travel across multiple time zones during the study * Current or recent mood disturbances or Axis I disorders (descriptions will be given) * Current misuse of alcohol and/or drugs * Current smoker * Recent (within the last 12 weeks) infection and/or use of antibiotic medication * Pregnant, seeking to become pregnant or lactating * Those using (including within the last 2 weeks) proton-pump inhibitors
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Cognition are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
Northumbria University- Northumbria Sleep center and NUTRAN
Newcastle upon Tyne, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a daily pill slow the visible signs of aging?
- 150,000 children to be tracked from birth to old age in massive health study
- Can free groceries and classes rewire daily health habits?
- Does soreness after exercise disrupt sleep more for people with insomnia?
- Can teaching parents about sleep help kids with developmental conditions?
- Can a rewired EMDR therapy ease the mental toll of migration?