Status:

COMPLETED

A Crossover Trial to Examine the Efficacy of a Powder to Improve Sleep Quality and Performance

Lead Sponsor:

Beam

Collaborating Sponsors:

Citruslabs

Conditions:

Sleep

Sleep Disorder

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This is a randomized, placebo-controlled crossover study to assess the efficacy of BEAM's Dream Powder in improving sleep health among 40 adults. Participants will use a placebo for 2 weeks, followed ...

Eligibility Criteria

Inclusion

  • 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

  • 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.

Key Trial Info

Start Date :

July 2 2024

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 17 2024

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT07183735

Start Date

July 2 2024

End Date

October 17 2024

Last Update

September 19 2025

Active Locations (1)

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1

Citruslabs

Las Vegas, Nevada, United States, 89118

A Crossover Trial to Examine the Efficacy of a Powder to Improve Sleep Quality and Performance | DecenTrialz