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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Rest Study Active Product 1.1 Usage | Participants will use Radicle Rest Active Product 1.1 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 1.2 Usage | Participants will use Radicle Rest Active Product 1.2 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 2.1 Usage | Participants will use Radicle Rest Active Product 2.1 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 2.2 Usage | Participants will use Radicle Rest Active Product 2.2 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Placebo Control Form 1 | Participants will use Placebo Control Form 1 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Placebo Control Form 2 | Participants will use Placebo Control Form 2 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Placebo Control Form 3 | Participants will use Placebo Control Form 3 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 3.1 Usage | Participants will use Radicle Rest Active Product 3.1 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Placebo Control Form 4 | Participants will use Placebo Control Form 4 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 4.1 Usage | Participants will use Radicle Rest Active Product 4.1 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 4.2 Usage | Participants will use Radicle Rest Active Product 4.2 as directed for a period of 6 weeks. |
| DIETARY_SUPPLEMENT | Rest Study Active Product 4.3 Usage | Participants 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.