Using Vegetable and Berry Products Can Improve Skin Conditions

February 1, 2021 updated by: TCI Co., Ltd.
Hypothesis: vegetable and berry products for 8 weeks can improve skin condition

Study Overview

Detailed Description

Hypothesis: Using vegetable and berry products for 8 weeks can improve skin condition

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Neipu Township
      • Taipei, Neipu Township, Taiwan, 100225
        • Research & Design Center, TCI CO., Ltd

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Dry skin
  2. Rough skin
  3. Large pores
  4. Dark yellow complexion
  5. Sagging skin

Exclusion Criteria:

  1. Skin disorders
  2. Liver diseases
  3. Kidney diseases
  4. Allergy to cosmetics, drugs, or foods
  5. Pregnant and lactating women
  6. People who had any cosmetic procedures before 4 weeks of the study
  7. Area of facial spot over 3 cm2
  8. Vegan
  9. People who took collagen supplements in the past 3 months.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: placebo group
subjects drank 50 ml , 1 bottle a day for 8 week
subjects drank 50 ml , 1 bottle a day for 8 week
Experimental: Vegetable and Berry Drink
subjects drank 50 ml , 1 bottle a day for 8 week
subjects drank 50 ml , 1 bottle a day for 8 week

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
skin elasticity
Time Frame: up to 8 week
using cutometer dual MPA580 to examine skin elasticity (The closer the R2 value is to 1, the better the elasticity and no unit)
up to 8 week
skin gloss
Time Frame: up to 8 week
using probe system GL2000 & MPA10 to examine skin gloss (The higher the value, the higher the gloss, no unit)
up to 8 week
skin spot
Time Frame: up to 8 week
usig VISIA-CR to examine skin spot (The higher the value, the larger the pore area, mm2)
up to 8 week
skin wrinkle
Time Frame: up to 8 week
using VISIOSCAN-VC20 to examine skin wrinkle (The higher the value, the more wrinkles, surface evaluation of wrinkles, SEW)
up to 8 week
skin moisture
Time Frame: up to 8 week
using corneometer CM825 to examine skin moisture (The higher the value, the more water content, C.U., corneometer units ).subjects drank 50 ml after meal
up to 8 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2017

Primary Completion (Actual)

July 31, 2018

Study Completion (Actual)

October 31, 2018

Study Registration Dates

First Submitted

January 26, 2021

First Submitted That Met QC Criteria

February 1, 2021

First Posted (Actual)

February 2, 2021

Study Record Updates

Last Update Posted (Actual)

February 2, 2021

Last Update Submitted That Met QC Criteria

February 1, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 20180905VAB

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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