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NCT07009093 | RECRUITING | Breast Cancer


Utility of a Mobile Application for Young Women With Breast Cancer
Sponsor:

Wake Forest University Health Sciences

Brief Summary:

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.

Condition or disease

Breast Cancer

Cancer Distress

Intervention/treatment

Mighty Pro Application

Phase

NA

Detailed Description:

This is a prospective, randomized, two stage study. The target population is adult females ≥ 18 and ≤ 45 years of age with breast cancer with a National Comprehensive Cancer Network (NCCN) Distress Thermometer score of distress score ≥ 4. The study will be conducted at Atrium Health Wake Forest Baptist Comprehensive Cancer Center (AHWFBCCC). The hypothesis is that the social connectivity via the Mighty Pro Application, as well as the educational components available in the application, will decrease patients' cancer-related distress. This study aims to evaluate the feasibility of implementing the Mighty Pro Application and measure its efficacy at reducing distress among young women with breast cancer.

Study Type : INTERVENTIONAL
Estimated Enrollment : 120 participants
Masking : NONE
Primary Purpose : SUPPORTIVE_CARE
Official Title : Utility of a Mobile Application for Young Women With Breast Cancer
Actual Study Start Date : 2026-04
Estimated Primary Completion Date : 2027-07
Estimated Study Completion Date : 2030-01

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years to 45 Years
Sexes Eligible for Study: FEMALE
Accepts Healthy Volunteers:
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

Utility of a Mobile Application for Young Women With Breast Cancer

Location Details

NCT07009093


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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


RECRUITING

United States, North Carolina

Atrium Health Levine Cancer

Charlotte, North Carolina, United States, 28204

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