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Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients.

Cleo A SamuelAngela B SmithWendi ElkinsJennifer RichmondZahra MahboobaEthan BaschAntonia V BennettArlene E ChungMattias JonssonRonald C ChenBryce B Reeve
Published in: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation (2020)
Electronic patient-reported outcomes are perceived as valuable for variable reasons by Black and White cancer populations, with greater perceived value for communicating with clinicians reported among Blacks. To optimize equitable uptake of ePROs, oncology practices should offer several ePRO options (e.g., web-based, phone-based), as well as paper-based options, and consider the e-health literacy needs of patients during implementation.
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