Breast Cancer Clinical Trial
Project Insight: Feasibility of a Breast Cancer Screening Decision Support Tool
The purpose of this investigation is to conduct a feasibility study to evaluate the potential for implementing the developed decision support tool with Latina, Black, and non-Latina White women. The investigators will collect feasibility data and assess the use of the decision support tool with end-users. The aim is to determine if women using the decision support tool make more informed choices measured by knowledge, attitudes, and intentions.
Latina, Black, or non-Latina White women
Between the ages of 40-49 years
Can write, read, and understand English
-Women with greater than an average self-reported risk of breast cancer will be ineligible for participation, as evidenced by any of the following:
Self-reported personal history of breast cancer (invasive, ductal carcinoma in situ [DCIS], or lobular carcinoma in situ[LCIS])
Self-reported personal history of atypical hyperplasia
Self-reported first degree family member with history of breast cancer (e.g., mother, sister)
Self-reported known underlying genetic mutation such as a BRCA1/BRCA2 gene
Self-reported prior thoracic or chest wall radiation therapy
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There is 1 Location for this study
Saint Louis Missouri, 63110, United States
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