RECRUITING

Radicle Energy™ 24_RCA: A Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes

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Conditions

Fatigue

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

A randomized, double-blind, placebo-controlled direct-to-consumer study assessing the impact of health and wellness products on fatigue and related health outcomes

Official Title

Radicle Energy™ 24_RCA: A Randomized, Double-Blind, Placebo-Controlled Direct-to-Consumer Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes

Quick Facts

Study Start:2025-09-09
Study Completion:2026-09-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07166523

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults, at least 21 years of age at the time of electronic consent, inclusive of all ethnicities, races, and gender identities
  2. * Assigned sex at birth will determine sex-specific recruitment and surveys (male vs female) employed, when needed
  3. * Resides in the United States
  4. * Has the opportunity for at least 30% improvement in their primary health outcome
  5. * Expresses a willingness to take a study product and not know the product identity (active or placebo) until the end of the study
  1. * Report being pregnant, trying to become pregnant, or breastfeeding
  2. * Unable to provide a valid US shipping address and mobile phone number
  3. * Reports current enrollment in another clinical trial
  4. * Reports being a heavy drinker (defined as drinking 3 or more alcoholic beverages per day)
  5. * Unable to read and understand English
  6. * Reports a current and/or recent (up to 3 months ago) major illness and/or surgery that poses a known, significant safety risk.
  7. * 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.
  8. * Reports taking medications that have a well-established moderate or severe interaction, posing a substantial safety risk with any of the study product ingredients.
  9. * 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 safety risk
  10. * Lack of reliable daily access to the internet

Contacts and Locations

Study Contact

Study Manager
CONTACT
858-779-0086
studymgmt@radiclescience.com
Susan Hewlings
CONTACT
susan.hewlings@radiclescience.com

Principal Investigator

Susan Hewlings
PRINCIPAL_INVESTIGATOR
Radicle Science

Study Locations (Sites)

Radicle Science Inc.
Del Mar, California, 92014
United States

Collaborators and Investigators

Sponsor: Radicle Science

  • Susan Hewlings, PRINCIPAL_INVESTIGATOR, Radicle Science

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-09-09
Study Completion Date2026-09-09

Study Record Updates

Study Start Date2025-09-09
Study Completion Date2026-09-09

Terms related to this study

Additional Relevant MeSH Terms

  • Fatigue