A Pilot Study to Evaluate the Expanded Reach of Decentralized Digital Skin Health Clinical Studies

Completed

Conditions studied: Skin Aging, Hair Care, Skin Microbiome

In brief

This is a randomized, decentralized, non-interventional clinical study. The primary objective of this study is to develop execution and efficiency metrics from completion of this study to inform on the potential design for future projects. The secondary objective of this study is to assess the main study endpoints across balanced attributes of study sub-populations.

Key facts

Study ID

NCT07193290

Run by

Kenvue Brands LLC

People needed

1027

Starts

2025-05-13

Expected to finish

2025-10-01

Last updated by the study team

2026-08-05

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Self-reported Monk skin type 1 to 10, targeting to complete at least 100 subjects for each Monk skin type.
• 18 to 65 years old, targeting to complete:
• 18- to 40-year-old age range: at least 50 subjects within each Monk type
• 41- to 65-year-old age range: at least 50 subjects within each Monk type
• Lives within an Inner City, Urban, Suburban, or Rural community type (as determined by self-report or provided zip code), targeting to complete:
• Inner City/Urban community type: at least 25 subjects within each age range and Monk type
• Suburban/Rural community type: at least 25 subjects within each age range and Monk type
• Has electronically accepted the Consent for Photograph Release and ICD including Health Insurance Portability and Accountability Act (HIPAA) disclosure.
• Has a personal smartphone with a camera and an internet connection (wi-fi, cellular services, etc.).
• Intends to complete the study and willing and able to follow all study instructions.

You may not qualify if…

• Has known allergies or adverse reactions to topical adhesives.
• Is simultaneously participating in any other clinical study for the duration of this study or has participated in any product-use study within 30 days prior to remote Visit 1.
• Is an employee/contractor or immediate family member of the PI, study technology provider, laboratory, or Sponsor.

Where it is running

• Laina Enterprises, Inc. — Apopka, Florida, United States

Full record on ClinicalTrials.gov

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