SUSPENDED

My Skin & Hair Journey_virtual Registry

Conditions

Quick Navigation

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 longitudinal, observational, direct to participant registry to better understand biological, clinical, and environmental aspects of skin/hair health and beauty.

Official Title

My Skin & Hair Journey_virtual Registry

Quick Facts

Study Start:2023-06-30

Study Completion:2025-11-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:SUSPENDED

Study ID

NCT06066463

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 70 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion 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)	Pregnancy or breastfeeding Severe psychiatric disorders Active substance abuse Unstable medical conditions Inability to comply with study requirements

Inclusion Criteria

Exclusion 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)

Pregnancy or breastfeeding
Severe psychiatric disorders
Active substance abuse
Unstable medical conditions
Inability to comply with study requirements

Contacts and Locations

Principal Investigator

KRISDA CHAIYACHATI, MD MPH FACP

PRINCIPAL_INVESTIGATOR

Verily Life Sciences

Study Locations (Sites)

Verily Life Sciences

South San Francisco, California, 94080

United States

Collaborators and Investigators

Sponsor: L'Oreal

KRISDA CHAIYACHATI, MD MPH FACP, PRINCIPAL_INVESTIGATOR, 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 Registration Dates

Study Start Date2023-06-30

Study Completion Date2025-11-30

Study Record Updates

Study Start Date2023-06-30

Study Completion Date2025-11-30

Terms related to this study

Additional Relevant MeSH Terms

Skin
Hair