RECRUITING

A Skin Image Reference Tool to Aid Healthcare Providers' Diagnosis

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

Consented patients will have three images taken of their dermatologic conditions within the Belle.ai software. These images will be uploaded and saved within the Belle software system where a single AI-generated differential list will be generated based on the three photos. All photos uploaded will be de-identified. The software will not have any unique identifiers of participants saved in the system. The photos will be named based on participant enrollment numbers or unique code numbers and no unique identifiers will be attached to the photos. There will be no data collection form necessary for this study

Official Title

A Skin Image Reference Tool to Aid Healthcare Providers' Diagnosis of Commonly Encountered Dermatologic Diseases

Quick Facts

Study Start:2025-09-15
Study Completion:2027-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07033169

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:10 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patient must present to an Advocate Health dermatology clinic
  2. * Patient must have the ability and willingness to provide informed consent and comply with study procedures and visits
  3. * Participant dermatologists must have access to the required technology (e.g., smartphone with internet access) and be capable of using it for the required image capture
  1. * Patients who are unable to comply with study procedures due to physical or mental health limitations (as assessed by study coordinator)
  2. * Pediatric, adolescent, and teen patients who present with dermatological conditions on their genitalia will not be included in the study (in support of patient privacy concerns).

Contacts and Locations

Study Contact

Irma M Richardson, MHA
CONTACT
336-716-2903
irichard@wakehealth.edu

Principal Investigator

Lindsay C Strowd, MD
PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences

Study Locations (Sites)

Wake Forest University Health Sciences Department of Dermatology
Winston-Salem, North Carolina, 27157
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Lindsay C Strowd, MD, PRINCIPAL_INVESTIGATOR, Wake Forest University Health 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 Date2025-09-15
Study Completion Date2027-12

Study Record Updates

Study Start Date2025-09-15
Study Completion Date2027-12

Terms related to this study

Keywords Provided by Researchers

  • artificial intelligence
  • skin diseases
  • dermatology

Additional Relevant MeSH Terms

  • Dermatologic Disease