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Recruiting
NCT05609435
Intervention to Improve the Delivery of Follow-up Care for Low-Risk Breast Cancer
Conditions: Breast Cancer
Sex: Female
Ages: 18 Years – 95 Years
Phase: NA
Enrollment: 100
Sponsor: University of Wisconsin, Madison
Location: United States
Summary
This study tests a novel intervention designed to optimize needed survivorship care for low-risk breast cancer survivors while reducing burdensome care with limited health benefits.
This study examines whether the intervention, titled REASSURE, improves survivors' preparedness for survivorship.
100 participants will be on study for up to 18 months.
Eligibility Criteria
Inclusion Criteria:History of stage I, ER and/or PR positive, her2neu negative breast cancer≥6-24 months from diagnosisWilling to complete study procedures using emailExclusion Criteria:Receipt of chemotherapyNon-English speakersPregnancy, based on patient self-report.
If a patient becomes pregnant during the study period, they will be removed from the study at that time.
Source: ClinicalTrials.gov (NCT05609435). StuddyBuddy aggregates publicly available trial information.
