- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06066463
My Skin & Hair Journey_virtual Registry
Study Overview
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
Enrollment (Estimated)
Contacts and Locations
Study Locations
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California
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South San Francisco, California, United States, 94080
- Verily Life Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
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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.
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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
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18 months
|
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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)
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18 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: KRISDA CHAIYACHATI, MD MPH FACP, Verily Life Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ACR/MYSH/23-05335
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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