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

B

Beam

Status

Completed

Conditions

Sleep Disorder
Sleep

Treatments

Dietary Supplement: BEAM Dream Powder
Dietary Supplement: Placebo Control

Study type

Interventional

Funder types

Industry

Identifiers

NCT07183735
20417 (Other Identifier)

Details and patient eligibility

About

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 by the test product for 4 weeks, with sleep data collected via questionnaires and a Fitbit sleep tracker.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

40 participants in 2 patient groups, including a placebo group

BEAM Dream Powder
Experimental group
Treatment:
Dietary Supplement: BEAM Dream Powder
Placebo
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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