The goal of this clinical trial is to evaluate a nutritional supplement in an otherwise healthy adult population. The main questions it aims to answer are: * Do antioxidant carotenoid levels increase in after supplementation as measured by a non-invasive device? * Do wellness factors correlate with supplementation? Researchers will compare the nutritional supplement arm to a placebo group to assess its effects. Participants will take either the nutritional supplement or placebo once daily for 8 weeks. Participants will be scanned by a non-invasive hyperspectral absorption device to obtain a skin carotenoid score. Participants will also have facial images taken, dermal spectrophotometry measurements of their face, and complete self-assessment questionnaires.
Age range
20 Years – 60 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Skin carotenoid score via Prysm iO device
Timeframe: 8 weeks
Short-Form 36 Health Survey
Timeframe: 8 weeks
Skin color measurement via Spectrophotometer
Timeframe: 8 weeks
Perceived Immunity
Timeframe: 8 weeks
Psychological Scales Related to Physical Condition
Timeframe: 8 weeks
Fatigue and Vitality Status Assessment
Timeframe: 8 weeks
Brief Resilience Scale (BRS)
Timeframe: 8 weeks