Trials / Recruiting
RecruitingNCT07285109
The Impact of Qualia Vitamin C+ on Blood Vitamin C Levels
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 36 (estimated)
- Sponsor
- Qualia Life Sciences · Industry
- Sex
- All
- Age
- 25 Years
- Healthy volunteers
- Accepted
Summary
This is a randomized, double-blind, placebo-controlled, parallel-group, study evaluating the effect of a Qualia Vitamin C+ formulation on Whole Blood Vitamin C levels in the blood of healthy adults aged 25 years or older. Approximately 36 participants will be randomized to one of two study arms: Qualia Vitamin C+ or placebo. Each participant will take two capsules of their assigned product once daily in the morning, with or without food, over a 28-day period. The primary outcome is the change in blood vitamin C levels, assessed via in lab blood collection at baseline and study completion. Secondary endpoints include questionnaires measuring health-related cognitive functioning and stress (PROMIS Cognitive Function - Short Form 8a and the Perceived Stress Scale-10), the Single-item Assessment of Immune Fitness, evaluation of safety and tolerability, and an Overall Experience Questionnaire (Appendices 1, 4-7). All assessments, including electronic questionnaires, are completed remotely without in-person visits.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Qualia Vitamin C+ | Qualia Vitamin C+ manufactured by Qualia Life Sciences |
| DIETARY_SUPPLEMENT | Placebo | Rice flour |
Timeline
- Start date
- 2025-12-22
- Primary completion
- 2026-02-11
- Completion
- 2026-02-11
- First posted
- 2025-12-16
- Last updated
- 2025-12-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07285109. Inclusion in this directory is not an endorsement.