Study Stopped
recruitment issue
My Skin & Hair Journey_virtual Registry
1 other identifier
observational
10,000
1 country
1
Brief Summary
This is a longitudinal, observational, direct to participant registry to better understand biological, clinical, and environmental aspects of skin/hair health and beauty.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2023
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 30, 2023
CompletedFirst Submitted
Initial submission to the registry
September 27, 2023
CompletedFirst Posted
Study publicly available on registry
October 4, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2025
CompletedNovember 3, 2025
October 1, 2025
1.3 years
September 27, 2023
October 30, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Collect and organize a longitudinal skin & hair beauty registry
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 Outcomes (2)
Build and improve generalizable beauty knowledge
18 months
improve insights from longitudinal data
18 months
Interventions
Self reported female gender
Eligibility Criteria
healthy Female self declared
You may qualify if:
- Willing and able to provide informed consent
- Willing and able to provide applicable privacy authorization(s)
- Current resident of the United States
- 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)
You may not qualify if:
- \- Employee of the Sponsor(s), contracted research organizations, or virtual research sites
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- L'Oreallead
- Verily Life Sciencescollaborator
Study Sites (1)
Verily Life Sciences
South San Francisco, California, 94080, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
KRISDA CHAIYACHATI, MD MPH FACP
Verily Life Sciences
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 18 Months
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 27, 2023
First Posted
October 4, 2023
Study Start
June 30, 2023
Primary Completion
October 30, 2024
Study Completion
November 30, 2025
Last Updated
November 3, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share