Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07383974

The Impact of 12 Week Retention of Nutrients on Skin and the Perception of Physical Health Status

Led by ChinaNorm · Updated on 2026-02-03

120

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a randomized, double-blind, placebo-controlled clinical trial exploring the effects of a 12-week dietary supplement regimen on skin condition and perceived overall health status. The study will involve 120 healthy Chinese adults aged 18 and above with low daily fruit and vegetable intake. Participants will be randomly assigned to one of two groups: one group will take a combination of Nu Skin's Vitamin C \& Green Tea Capsules and Multivitamin \& Mineral Capsules, while the other group will take a matching placebo. The primary goal is to assess if the supplement combination improves skin health after 12 weeks, measured through specialized facial imaging (assessing spots, redness, evenness) and probe measurements (assessing elasticity, moisture, gloss). Secondary goals include evaluating changes in participants' self-perceived health status (via quality of life, fatigue, and digestive health questionnaires), psychological resilience, memory, and exploring a new method for measuring skin carotenoid levels. This study is not intended to verify the approved health functions of the products but to explore the potential combined effects of antioxidant and nutritional supplementation on skin and general well-being.

CONDITIONS

Official Title

The Impact of 12 Week Retention of Nutrients on Skin and the Perception of Physical Health Status

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Chinese adults of Asian descent aged 18 and above
  • Daily fruit and vegetable intake less than 240 grams
  • Skin Carotenoid Index (S3 measurement) less than 30000
  • Ability to read and understand basic Chinese and independently complete questionnaires
  • Voluntary participation with signed informed consent
  • Willingness to comply with all study evaluations
Not Eligible

You will not qualify if you...

  • Open facial skin lesions, visible scars, acne marks, or skin lesions on face or hand measurement areas
  • Symptoms of skin disease on face or hand measurement areas
  • Medical aesthetic procedures within the last 6 months
  • Participation in other clinical trials involving product use within the last 3 months
  • Use of health or nutritional supplements within the last 1 month
  • Planning pregnancy, pregnant, or lactating
  • Presence of any disease currently being treated
  • Any health issues or chronic diseases affecting behavior or cognition
  • Other medical reasons identified by experts that may affect study results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai China-norm Quality Technical Service Co., Ltd.

Shanghai, Shanghai Municipality, China, 200072

Actively Recruiting

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Research Team

Y

Yanwen Jiang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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