Radicle Relaxation™ 24_VNS: A Study Assessing the Impact of Health and Wellness Products on Stress and Related Health Outcomes

Eligibility Criteria

• * Resides in the United States
• * Has the opportunity for at least 30% improvement in their primary health outcome ● Expresses a willingness to take a study product and not know the product identity (active or placebo) until the end of the study
• * Report being pregnant, trying to become pregnant, or breastfeeding
• * Unable to provide a valid US shipping address and mobile phone number ● Reports current enrollment in another clinical trial
• * Reports being a heavy drinker (defined as drinking 3 or more alcoholic beverages per day)
• * Unable to read and understand English
• * Reports a current and/or recent (up to 3 months ago) major illness and/or surgery that poses a known, significant safety risk.
• * Reports a diagnosis of cardiac dysfunction, liver or kidney disease that presents a known contraindication and/or a significant safety risk with any of the study product ingredients.
• * Reports taking medications that have a well-established moderate or severe interaction, posing a substantial safety risk with any of the study product ingredients. o Anticoagulants, antihypertensives, anxiolytics, antidepressants, chemotherapy, immunotherapy, sedative hypnotics, seizure medications, medications that warn against grapefruit consumption, corticosteroids at doses greater than 5 mg per day, diabetic medications, oral anti-infectives (antibiotics, antifungals, antivirals) to treat an acute infection, antipsychotics, MAOIs, or thyroid products
• * Reports current use of the primary ingredient(s) and/or similar product(s) to the active study product(s) that may limit the effects of the study products and/or pose a known safety risk
• * Lack of reliable daily access to the internet