A Study Of Breast Cancer Screening And Clinical Trial Participation In Low Income And Rural Populations

Overview

About this study

The purpose of this project is to address disparities in breast cancer screening, outcomes and clinical research participation among rural and low-income women. By fostering engagement early and enhancing research readiness prior to disease onset, the project seeks to empower women as informed health advocates. By empowering women as informed health advocates and strengthening community partnerships, the program aims to reduce structural barriers and improve long‑term breast cancer outcomes in underserved populations.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria: FINALIZED by the CRC over phone

Participants must:

  • Self-identify as female.

  • Be between the ages of 50 and 74 years.

  • Have no prior history of breast cancer screening (i.e., who have either never received a mammogram or have not had one in the past five years)

  • Reside in a rural community (RUCA Code ≥ 4) in Wisconsin or belong to low SES (HOUSES: Q1-2)

  • Be able to speak and understand English or Spanish.

  • Be willing and able to provide informed consent.

Exclusion Criteria:

Participants will be excluded if they:

  • Women who have received a mammogram within the past five years.

  • Have a current or prior diagnosis of breast cancer.

  • Are currently undergoing treatment for any active malignancy.

  • Have cognitive or psychiatric impairments that, in the judgment of the study team, would preclude meaningful participation.

  • Do not speak English or Spanish, due to limitations in translation and interpreter availability.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 9/02/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Eau Claire, Wis.

Mayo Clinic principal investigator

Pravesh Sharma

Open for enrollment

Contact information:

Stephanie Larson

(715) 838-1976

Larson.Stephanie3@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20597361

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