Actively Recruiting

Phase Not Applicable
Age: 21Years - 105Years
All Genders
Healthy Volunteers
NCT07245784

Radicle Clarity™ RBB: A Study Assessing the Impact of Health and Wellness Products on Cognitive Function and Related Health Outcomes

Led by Radicle Science · Updated on 2025-12-22

850

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

R

Radicle Science

Lead Sponsor

J

Jeff Bland

Collaborating Sponsor

AI-Summary

What this Trial Is About

A Randomized, Double-Blind, Placebo-Controlled Study Assessing the Impact of Health and Wellness Products on Cognitive Function and Related Health Outcomes

CONDITIONS

Official Title

Radicle Clarity™ RBB: A Study Assessing the Impact of Health and Wellness Products on Cognitive Function and Related Health Outcomes

Who Can Participate

Age: 21Years - 105Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults, at least 21 years of age at the time of electronic consent, inclusive of all ethnicities, races, and gender identities
  • Assigned sex at birth will determine sex-specific recruitment and surveys (male vs female) employed, when needed
  • 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
Not Eligible

You will not qualify if you...

  • 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 significant safety risk with any of the study product ingredients, including NYHA Class III or IV congestive heart failure, atrial fibrillation, uncontrolled arrhythmias, cirrhosis, end-stage liver disease, stage 3b or 4 chronic kidney disease, or kidney failure
  • Reports taking medications with a well-established moderate or severe interaction posing a substantial safety risk with any study product ingredients, including anticoagulants, antihypertensives, anxiolytics, antidepressants, chemotherapy, immunotherapy, sedative hypnotics, seizure medications, medications warning against grapefruit consumption, corticosteroids over 5 mg per day, diabetic medications, oral anti-infectives for acute infections, antipsychotics, MAOIs, or thyroid products
  • Reports current use of the primary ingredient(s) and/or similar products to the active study products that may limit study product effects
  • Lack of reliable daily access to the internet

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Radicle Science Inc.

Del Mar, California, United States, 92014

Actively Recruiting

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Research Team

S

Study Manager

CONTACT

S

Susan Hewlings

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Radicle Clarity™ RBB: A Study Assessing the Impact of Health and Wellness Products on Cognitive Function and Related Health Outcomes | DecenTrialz