Purpose

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.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 45 Years
Eligible Sex
Female
Accepts Healthy Volunteers
No

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

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Supportive Care
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Access to the Mighty Pro Application
Participants will be given access to the Mighty Pro Application for 12 months.
  • Other: Mighty Pro Application
    Access to Mighty Pro Application
No Intervention
No Access to the Mighty Pro Application
Participants will not be given access to the Mighty Pro Application.

Recruiting Locations

Atrium Health Levine Cancer
Charlotte, North Carolina 28204
Contact:
Maggie Dzhanumova
704-754-3768
margarita.dzhanumova@advocatehealth.org

More Details

Status
Recruiting
Sponsor
Wake Forest University Health Sciences

Study Contact

Maggie Dzhanumova
704-754-3768
margarita.dzhanumova@advocatehealth.org

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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.