RECRUITING

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

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Conditions

Skin AgingHair CareSkin Microbiome

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2025-05-13
Study Completion:2025-10-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07193290

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.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-reported Monk skin type 1 to 10, targeting to complete at least 100 subjects for each Monk skin type.
  2. * 18 to 65 years old, targeting to complete:
  3. * 18- to 40-year-old age range: at least 50 subjects within each Monk type
  4. * 41- to 65-year-old age range: at least 50 subjects within each Monk type
  5. * Lives within an Inner City, Urban, Suburban, or Rural community type (as determined by self-report or provided zip code), targeting to complete:
  6. * Inner City/Urban community type: at least 25 subjects within each age range and Monk type
  7. * Suburban/Rural community type: at least 25 subjects within each age range and Monk type
  8. * Has electronically accepted the Consent for Photograph Release and ICD including Health Insurance Portability and Accountability Act (HIPAA) disclosure.
  9. * Has a personal smartphone with a camera and an internet connection (wi-fi, cellular services, etc.).
  10. * Intends to complete the study and willing and able to follow all study instructions.
  1. * Has known allergies or adverse reactions to topical adhesives.
  2. * 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.
  3. * Is an employee/contractor or immediate family member of the PI, study technology provider, laboratory, or Sponsor.

Contacts and Locations

Study Contact

Kenvue Global Clinical Operations
CONTACT
18779295131
KenvueClinical_KV@kenvue.com

Study Locations (Sites)

Laina Enterprises, Inc.
Apopka, Florida, 32712
United States

Collaborators and Investigators

Sponsor: Kenvue Brands LLC

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 Registration Dates

Study Start Date2025-05-13
Study Completion Date2025-10-31

Study Record Updates

Study Start Date2025-05-13
Study Completion Date2025-10-31

Terms related to this study

Additional Relevant MeSH Terms

  • Skin Aging
  • Hair Care
  • Skin Microbiome