Evaluation of Perceived Outcomes With AGZ: A Randomized, Controlled, Consumer Perception Study

Athletic Greens International

Summary

The study will be a prospective randomized, controlled clinical study. There will be interventional treatment for a total of 30 days. The subjects will complete questionnaires throughout the study at pre-specified timepoints.

Eligibility

Age range: 22–59 years
Sex: All
Healthy volunteers: Yes

Detailed criteria

Inclusion Criteria: * Male or female. * Age 25-59 years. * BMI ≥18.5 and ≤29.9 kg/m². * Currently experiencing issues with sleep quality, falling asleep, staying asleep, or waking during the night. * RU-SATED score ≤17. * Willing and able to follow the study protocol. * Willing to discontinue any other supplements (including nootropics, adaptogens, calming herbs), medications, herbal remedies, or over-the-counter sleep medications (e.g., zolpidem, diphenhydramine, Benadryl, ZzzQuil, Unisom, magnesium or melatonin products) used to assist with sleep during the study. * Agree to limit alcohol i…

Interventions

Dietary Supplement
Sleep Supplement
Powdered sleep supplement

Location

Alethios (Virtual Study Platform)
San Francisco, California
support@alethios.com 6502068006

Evaluation of Perceived Outcomes With AGZ: A Randomized, Controlled, Consumer Perception Study

Summary

Eligibility

Interventions

Location

Compensation

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Details

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