COMPLETED

Breast Cancer AI Imaging Study

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 study aims to develop a social health platform called MammoChat (https://MammoChat.com) that allows patients to share their real-world patient data to a trusted network for development of clinical intelligence to improve patient outcomes. Therefore: 1. The investigator will establish a Discourse social network where patients can anonymously and securely share their breast imaging and interact with other patients. 2. The investigator will use standardized questionnaires to understand the impact of use of the social network on outcomes related to breast cancer screening such as anxiety. 3. The investigator will assemble a crowdsourced, de-identified radiographic repository for training, testing, and validating AI models aimed at earlier and more accurate disease detection for breast cancer.

Official Title

Elucidating the Impact of Social Wellness and Artificial Intelligence on the Psychological Consequences of Breast Cancer Imaging

Quick Facts

Study Start:2024-09-05
Study Completion:2025-09-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06604078

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults, ages 18 and older
  2. * Had a radiographic breast cancer imaging test, either for screening or diagnosis of breast cancer, with either positive or negative results performed in a US institution.
  3. * Have an email account with access to a reliable internet connection or smartphone
  1. * Minors , ages under 18
  2. * Prisoners. Given the repository design, prisoners are unlikely to participate and provide a consent
  3. * Adults who are unable to provide consent.

Contacts and Locations

Principal Investigator

Dexter Hadley, M.D., PhD, M.S.E
PRINCIPAL_INVESTIGATOR
University of Central Florida

Study Locations (Sites)

University of Central Florida
Orlando, Florida, 32827
United States

Collaborators and Investigators

Sponsor: University of Central Florida

  • Dexter Hadley, M.D., PhD, M.S.E, PRINCIPAL_INVESTIGATOR, University of Central Florida

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 Date2024-09-05
Study Completion Date2025-09-01

Study Record Updates

Study Start Date2024-09-05
Study Completion Date2025-09-01

Terms related to this study

Keywords Provided by Researchers

  • Breast Cancer
  • Artifical Inteligence
  • AI

Additional Relevant MeSH Terms

  • Breast Cancer
  • Breast Cancer Screening