Home › Breast Cancer › NCT07009093
Utility of a Mobile Application for Young Women With Breast Cancer
Recruiting
Who can join
Ages 18 to 45 · Women
Full eligibility criteria
Inclusion Criteria: * Ability to understand and willingness to sign an IRB-approved informed consent * Age ≥ 18 and ≤ 45 years at the time of consent * Female * Established patient at Atrium Health Wake Forest Baptist Comprehensive Cancer Center (AHWFBCCC) * Histological confirmation of any type and stage (0-IV) of breast cancer * Screening (baseline) NCCN Distress Thermometer score ≥ 4 * Access to a mobile device for trial purposes and an active email address * Ability to read and understand the English language. NOTE: The Mighty Pro Application is available in English only. * As determined by the enrolling Investigator, ability of the participant to understand and comply with study procedures for the entire length of the study Exclusion Criteria: \- None
About the study
This study aims to evaluate the use of mobile technology as a communication tool among patients with breast cancer and measured its effect on patient-reported cancer-related distress, specifically focusing on young women as they often face unique challenges.
What is being tested
- Mighty Pro Application (other)
Sponsor: Wake Forest University Health Sciences · Participants: 120 · Started: 2026-09
Contact the study team
- Maggie Dzhanumova · Phone: 704-754-3768
Official record on ClinicalTrials.gov — NCT07009093
Locations in the U.S.
| North Carolina | Atrium Health Levine Cancer, Charlotte |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.