Dream powder put to the test: will it beat a placebo for better sleep?
NCT ID NCT07183735
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested a powdered sleep supplement called BEAM Dream Powder in 40 adults who had trouble sleeping. For two weeks, participants took a placebo, then switched to the real powder for four weeks. Researchers used sleep questionnaires and Fitbit trackers to see if the powder improved sleep quality, restfulness, and energy levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BEAM Dream Powder (dietary supplement)
- What this could lead to
- If it works, this could point toward a natural supplement to help people with mild sleep issues fall asleep and feel more rested.
- What could go wrong
- This is a small, early-stage trial with only 40 people. The results may not apply to everyone, and the supplement might not work better than a 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
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40 people
The number who actually took part.
- Started
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Jul 2024
- Finished
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Oct 2024
- 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.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Male or female * 18+ years old * Self-reported issues with sleeping, falling asleep, or staying asleep. * Willing to discontinue any supplements, medications, herbal remedies, or melatonin products used to assist with sleep for the study duration. * Willing to avoid introducing any other supplements, medications, herbal remedies, or melatonin products used to assist with sleep for the duration of this trial. * Willing to maintain their standard sleep pattern and activity level for the duration of the study. * Be generally healthy and not live with any uncontrolled chronic disease. Exclusion Criteria: * Diagnosed with any chronic sleep condition, including but not limited to insomnia, narcolepsy, or sleep apnea. * Women who are pregnant, breastfeeding, or trying to conceive. * Anyone unwilling or unable to follow the study protocol. * Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders. * Is currently undergoing, or planning to undergo, any significant medical procedures during the study period. * Has undergone any surgeries or invasive treatments in the last six months. * A history of severe allergic reactions, including but not limited to any of the product's ingredients. * Anyone with a nut allergy. * Heavy drinkers. A heavy drinker is considered to be a woman who drinks 8 or more alcoholic drinks per week or a man who drinks 15 or more alcoholic drinks per week. * Anyone who uses illicit drugs. * Use any prescription medication, over-the-counter, or herbal remedies that can affect sleep. * Have a job that involves working the third or night shifts.
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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.
Contacts and locations
Locations
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Citruslabs
Las Vegas, Nevada, 89118, United States
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Other studies related to the condition(s) this trial covers.
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