Breast Cancer Clinical Trial
Metastatic Breast Cancer-Specific Prognostic Tool
Summary
In this qualitative study, Investigators will conduct semi-structured interviews with clinicians that are involved in the care of patients with breast cancer to evaluate the acceptability, appropriateness, and feasibility/usability of a metastatic breast cancer-specific prognostic tool. These interviews will be conducted by the UNC CHAI Core and will continue until thematic saturation (estimated 20-30 participants). The investigators will code the qualitative data using emerging themes, guided by a well-established implementation science theory, the Consolidated Framework for Implementation Research (CFIR). The information gained from these studies will inform an implementation approach to increase the usability and acceptability of a novel prognostic tool to assist oncologists in the prognosis of patients with metastatic breast cancer.
Full Description
If this study is successful, Investigators will implement an MBC-specific prognostic tool to help clinicians identify patients who are at high risk of death in the next 30 days. Based on the input from clinicians in this proposal, as well as additional qualitative studies with patients and families, Investigators will design an implementation protocol to inform how to use this tool in clinical practice. Rather than simply publishing a prognostic tool that may not be adopted into practice, this project aims to ensure successful implementation of an evidence-based tool into the routine care of patients with MBC. Doing so will serve as an important step towards identifying high-risk patients and connecting ort to ensure high-quality, patient-centered end-of-life care.
Eligibility Criteria
Inclusion Criteria:
In order to participate in this study a subject must meet ALL of the eligibility criteria outlined below.
Subjects is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee.
Diagnosis of metastatic breast cancer or primary caregiver for someone with a diagnosis of metastatic breast cancer
Age > 18 years
Verbal informed consent obtained to participate in the study.
Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee.
Exclusion Criteria:
1. Non-English speaking
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There is 1 Location for this study
Chapel Hill North Carolina, 27599, United States
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