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COMPLETED
NCT05609435
NA

Intervention to Improve the Delivery of Follow-up Care for Low-Risk Breast Cancer

Sponsor: University of Wisconsin, Madison

View on ClinicalTrials.gov

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. Up to 110 participants will be on study for up to 18 months.

Official title: Evaluating a Novel Follow-up Intervention to Improve the Delivery of Follow-up Care for Low-Risk Breast Cancer Survivors in Wisconsin

Key Details

Gender

FEMALE

Age Range

18 Years - 95 Years

Study Type

INTERVENTIONAL

Enrollment

104

Start Date

2022-11-16

Completion Date

2026-01-27

Last Updated

2026-04-14

Healthy Volunteers

No

Conditions

Interventions

OTHER

REASSURE

REASSURE is comprised of three components that are intended to be integrated into survivorship care at each follow-up visit: 1) An online patient-reported outcome (PRO) assessment to comprehensively evaluate survivors' symptoms and concerns; 2) A tailored follow-up recommendation based on pre-established thresholds for reported symptoms and concerns. Survivors who report symptoms or concerns have a follow-up visit to discuss findings whereas survivors without symptoms or concerns will avoid a follow-up visit; and 3) Online survivorship messaging sent after the visit, which includes reassurance about the low recurrence risk, an overview of what to expect from follow-up, and steps survivors can take to reduce cancer risk.

Locations (1)

UW Health Oncology Clinics

Madison, Wisconsin, United States