Trials / Not Yet Recruiting
Not Yet RecruitingNCT07342192
Radicle Clarity DSTTM: A Study Assessing the Impact of Health and Wellness Products on Mental Clarity and Related Health Outcomes
Radicle Clarity DSTTM: A Randomized, Double-Blind, Placebo-Controlled Direct-to-Consumer Study Assessing the Impact of Health and Wellness Products on Mental Clarity and Related Health Outcomes
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 990 (estimated)
- Sponsor
- Radicle Science · Industry
- Sex
- All
- Age
- 35 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
Radicle Clarity DSTTM: A randomized, double-blind, placebo-controlled direct-to-consumer study assessing the impact of health and wellness products on mental clarity and related health outcomes.
Detailed description
This is a randomized, double-blind, placebo-controlled study conducted with adult participants, residing in the United States. Eligible participants will (1) have the opportunity for meaningful improvement (at least 30%) in their primary health outcome, and (2) express acceptance in taking a product and not knowing its formulation until the end of the study. Participants that report a known cardiac dysfunction, liver or kidney disease may be excluded. Participants that report a known contraindication or with well-established, significant safety concerns due to illness will be excluded. Heavy drinkers and those who report they are pregnant, trying to become pregnant, or breastfeeding will be excluded. Participants that report taking medications with a known contraindication or with well-established, significant safety concerns will be excluded. Self-reported data are collected electronically from eligible participants for 12 weeks. Participant reports of health indicators will be collected at enrollment and throughout the active period of study product usage. 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 | Clarity Product Placebo Control | Participants will use their Clarity Product Placebo Control as directed for a period of 12 weeks. |
| DIETARY_SUPPLEMENT | RS Clarity Active Product | Participants will use their RS Clarity Active Product as directed for a period of 12 weeks |
Timeline
- Start date
- 2026-01-21
- Primary completion
- 2027-01-21
- Completion
- 2027-01-21
- First posted
- 2026-01-15
- Last updated
- 2026-01-15
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07342192. Inclusion in this directory is not an endorsement.