Evaluation of the Skin-Beautifying Effects of Collagen Drinks

March 26, 2025 updated by: Simply Plus Co., Ltd.
This study aims to investigate the skin beauty benefits of collagen drinks in healthy individuals.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

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

  • Taiwan
      • Tainan, Taiwan, 71710
        • Chia Nan University of Pharmacy & Science

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Age over 18 years
  2. Healthy people

Exclusion Criteria:

  1. Non-volunteer
  2. Pregnant and lactating women
  3. Hypersensitivity to the assigned product
  4. Diagnosed with skin diseases, liver diseases, kinedy disease, and other severe diseases
  5. Cosmetic, drug, or food allergies
  6. Concurrent aesthetic treatments (e.g., intense pulse light, medical peelings, or laser therapy)
  7. Aceepted aesthetic treatments one month ago before the study
  8. Chronic sun exposure (over 3 hours/day)
  9. The members of the research team

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Collagen Drinks
The Collagen Drinks contain collagen peptides and antioxidants
Dietary supplement: Collagen Drinks
Dosage: 50 mL/day; duration: 8 weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measurement of skin hydration
Time Frame: Week 0, 4, 8
Corneometer CM825 is used to measure the moisture of upper cheek
Week 0, 4, 8
Measurement of skin elasticity
Time Frame: Week 0, 4, 8
Cutometer® is used to measure the skin elasticity of upper cheek
Week 0, 4, 8
Measurement of skin wrinkles
Time Frame: Week 0, 4, 8
Visia® skin analysis system is used to measure the skin wrinkles of full face
Week 0, 4, 8
Measurement of skin pores
Time Frame: Week 0, 4, 8
Visia® skin analysis system is used to measure the skin spots of full face
Week 0, 4, 8
Measurement of collagen content
Time Frame: Week 0, 4, 8
DermaLab® Series SkinLab Combo (Cortex) is employed to measure skin collagen content of upper cheek
Week 0, 4, 8
Measurement of wrinkles around the eyes
Time Frame: Week 0, 4, 8
Visia® skin analysis system is used to measure the skin wrinkles around the eyes
Week 0, 4, 8
Measurement of skin brightness
Time Frame: Week 0, 4, 8
Chroma Meter MM500 is employed to measure the brightness of upper cheek
Week 0, 4, 8
Measurement of collagen levels in the blood
Time Frame: Week 0, 8
Analysis of changes in beauty-related biomarkers in the blood
Week 0, 8
Measurement of hyaluronic acid levels in the blood
Time Frame: Week 0, 8
Analysis of changes in beauty-related biomarkers in the blood
Week 0, 8
Measurement of superoxide dismutase (SOD) levels in the blood
Time Frame: Week 0, 8
Analysis of changes in beauty-related biomarkers in the blood
Week 0, 8

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The change of self-assessment skin condition
Time Frame: Week 0, 4, 8
A self-assessment questionnaire was collected and evaluate skin condition
Week 0, 4, 8

Collaborators and Investigators

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

Sponsor

Simply Plus Co., Ltd.

Collaborators

Chia Nan University of Pharmacy ＆ Science

Investigators

  • Principal Investigator: Chia-Hua Liang, Department of Cosmetic Science, Chia Nan University of Pharmacy ＆ Science

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)

January 13, 2025

Primary Completion (Estimated)

July 31, 2025

Study Completion (Estimated)

August 31, 2025

Study Registration Dates

First Submitted

March 26, 2025

First Submitted That Met QC Criteria

March 26, 2025

First Posted (Actual)

March 28, 2025

Study Record Updates

Last Update Posted (Actual)

March 28, 2025

Last Update Submitted That Met QC Criteria

March 26, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 25-007-B

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

product manufactured in and exported from the U.S.

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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