Registry to understand skin and hair health
My Skin & Hair Journey_virtual Registry
This study collects information from people to see how different factors affect skin and hair health over time and how these changes impact their quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | Female |
| Sponsor | L'Oreal Industry-sponsored |
| Locations | 1 site (South San Francisco, California) |
| Trial ID | NCT06066463 on ClinicalTrials.gov |
What this trial studies
This observational registry collects and analyzes data from participants to explore biological, clinical, and environmental factors affecting skin and hair health. By engaging participants over time, the study aims to gather insights into how skin health evolves and what influences these changes, focusing on participant perspectives and quality of life. The study also seeks to enhance data handling methods to improve the depth and applicability of findings related to skin and beauty health.
Who should consider this trial
Good fit: Ideal candidates are self-identified females aged 18 to 70 who are current residents of the United States and can engage with internet-based tools.
Not a fit: Patients who are employees of the sponsor or contracted organizations, or those unable to provide informed consent, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights that lead to improved skin and hair health management for participants.
How similar studies have performed: While this approach is innovative in its focus on participant-centric data collection, similar observational studies have shown success in understanding health conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
South San Francisco, California
- Verily Life Sciences — South San Francisco, California, United States (Recruiting)
Study contacts
- Principal investigator: Krisda Chaiyachati, Md Mph Facp — Verily Life Sciences
- Study coordinator: Gabriel Kowalsky
- Email: gkowalsky@verily.com
- Phone: 19709011616
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.