Clinical Trials Directory

Trials / Completed

CompletedNCT05657808

Radicle Rest 2: A Study of Health and Wellness Products on Sleep and Health Outcomes

Radicle™ Rest 2: A Randomized, Blinded, Placebo-Controlled Direct-to-Consumer Study of Health and Wellness Products on Sleep and Other Health Outcomes

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
4,152 (actual)
Sponsor
Radicle Science · Industry
Sex
All
Age
21 Years – 105 Years
Healthy volunteers
Accepted

Summary

A randomized, blinded, placebo-controlled direct-to-consumer study assessing the impact of health and wellness products on sleep and other health outcomes.

Detailed description

This is a randomized, blinded, placebo-controlled study conducted with adult participants, age 21 and older and residing in the United States. Eligible participants will (1) endorse a desire for improved sleep, (2) indicate an interest in taking a health and wellness product to potentially help their sleep, and (3) express acceptance in taking a product and not knowing its formulation until the end of the study. Participants with known liver or kidney disease, heavy drinkers, and those who report they are pregnant, trying to become pregnant, or breastfeeding will be excluded. Those taking certain medications will be excluded. Self-reported data are collected electronically from eligible participants over 7 weeks. Participant reports of health indicators will be collected during baseline, throughout the active period of study product use, and in a final survey. All study assessments will be electronic; there are no in-person visits or assessments for this real-world evidence study.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTRest Study Active Product 1.1 UsageParticipants will use Radicle Rest Active Product 1.1 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 1.2 UsageParticipants will use Radicle Rest Active Product 1.2 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 2.1 UsageParticipants will use Radicle Rest Active Product 2.1 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 2.2 UsageParticipants will use Radicle Rest Active Product 2.2 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTPlacebo Control Form 1Participants will use Placebo Control Form 1 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTPlacebo Control Form 2Participants will use Placebo Control Form 2 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTPlacebo Control Form 3Participants will use Placebo Control Form 3 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 3.1 UsageParticipants will use Radicle Rest Active Product 3.1 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTPlacebo Control Form 4Participants will use Placebo Control Form 4 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 4.1 UsageParticipants will use Radicle Rest Active Product 4.1 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 4.2 UsageParticipants will use Radicle Rest Active Product 4.2 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTRest Study Active Product 4.3 UsageParticipants will use Radicle Rest Active Product 4.3 as directed for a period of 6 weeks.

Timeline

Start date
2023-01-09
Primary completion
2023-12-04
Completion
2024-04-15
First posted
2022-12-20
Last updated
2024-05-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05657808. Inclusion in this directory is not an endorsement.