My Skin & Hair Journey_virtual Registry

October 30, 2025 updated by: L'Oreal
This is a longitudinal, observational, direct to participant registry to better understand biological, clinical, and environmental aspects of skin/hair health and beauty.

Study Overview

Status

Suspended

Conditions

Intervention / Treatment

Detailed Description

This is a longitudinal, observational, direct to participant registry to better understand biological, clinical, and environmental aspects of skin/hair health and beauty. By collecting, organizing, and analyzing data for a group of participants over time, researchers will use information to learn more about these topics. This study will collect long-term information about study participants, developing a lean, participant-centric approach to curating meaningful longitudinal data that incorporate participant perspectives including quality of life and personal beauty health preferences. This should allow researchers to understand how participant skin health changes over time and what factors can influence those changes with a specific focus on participant-centric learning.

Additionally, this study will look for ways to develop and/or improve data handling approaches to increase the depth, generalizability, and/or longitudinality of skin health and beauty data based on approaches that decrease burden, as appropriate, over time (eg, for study participants, investigators, clinical research stakeholders)

Study Type

Observational

Enrollment (Estimated)

10000

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

    • California
      • South San Francisco, California, United States, 94080
        • Verily Life Sciences

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

Sampling Method

Non-Probability Sample

Study Population

healthy Female self declared

Description

Inclusion Criteria:

  • Willing and able to provide informed consent
  • Willing and able to provide applicable privacy authorization(s)
  • Current resident of the United States
  • 18 to 70 years of age at the time of informed consent Self identified female gender
  • Able to read and understand English and/or Spanish
  • Ability to access internet based study-related tools (eg, applications, software, email notifications)
  • Willingness to use study web/mobile applications (eg, selfie assistant, air quality and weather monitoring)

Exclusion Criteria:

- Employee of the Sponsor(s), contracted research organizations, or virtual research sites

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Collect and organize a longitudinal skin & hair beauty registry
Time Frame: 18 months
Collect and organize a longitudinal skin & hair beauty registry that links skin & hair individual outcomes to lifestyle, environment, age and beauty perception on all skin diversity, and to make that information accessible and actionable for researchers and consumers.
18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Build and improve generalizable beauty knowledge
Time Frame: 18 months
Build and improve the broader longitudinal registry from various data sources inclusive of intentionally collected data and other supporting data to inform generalizable beauty knowledge
18 months
improve insights from longitudinal data
Time Frame: 18 months
Support the development and/or optimization of people, process, and technical approaches to improve insights from longitudinal data (eg, to improve research approaches, guide advances in precision beauty)
18 months

Collaborators and Investigators

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

Sponsor

Collaborators

Investigators

  • Principal Investigator: KRISDA CHAIYACHATI, MD MPH FACP, Verily Life Sciences

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)

June 30, 2023

Primary Completion (Actual)

October 30, 2024

Study Completion (Estimated)

November 30, 2025

Study Registration Dates

First Submitted

September 27, 2023

First Submitted That Met QC Criteria

September 27, 2023

First Posted (Actual)

October 4, 2023

Study Record Updates

Last Update Posted (Estimated)

November 3, 2025

Last Update Submitted That Met QC Criteria

October 30, 2025

Last Verified

October 1, 2025

More Information

Terms related to this study

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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