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Recruiting NCT07009093

NCT07009093 Utility of a Mobile Application for Young Women With Breast Cancer

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Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07009093
Status Recruiting
Phase —
Sponsor Wake Forest University Health Sciences
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2027-01
Primary Completion 2027-07

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 45 Years
Study Type INTERVENTIONAL
Interventions
Mighty Pro Application

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2027-01 with a primary completion date of 2027-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

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

Contact & Investigator

Central Contact

Maggie Dzhanumova

✉ margarita.dzhanumova@advocatehealth.org

📞 704-754-3768

Principal Investigator

Julie Fisher, MD

PRINCIPAL INVESTIGATOR

Wake Forest University Health Sciences

Frequently Asked Questions

Who can join the NCT07009093 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07009093 currently recruiting?

Yes, NCT07009093 is actively recruiting participants. Contact the research team at margarita.dzhanumova@advocatehealth.org for enrollment information.

Where is the NCT07009093 trial being conducted?

This trial is being conducted at Charlotte, United States.

Who is sponsoring the NCT07009093 clinical trial?

NCT07009093 is sponsored by Wake Forest University Health Sciences. The principal investigator is Julie Fisher, MD at Wake Forest University Health Sciences. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology