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
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 SupplementSleep Supplement
Powdered sleep supplement
Location
- Alethios (Virtual Study Platform)San Francisco, California