Solid Tumor, Adult Clinical Trial
Official title:
Feasibility of a Process of Digital Validation of Outpatients Chemotherapies in a Day Treatment Unit
The aim of CPV 2.0 study is to evaluate a process of digital prevalidation of outpatients
chemotherapy thanks to a numeric application. This digital tool is based on the combination
of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common
Terminology Criteria for Adverse Events (PRO-CTCAE) to a decisional algorithm.
After cycle 1, chemotherapy digital prevalidation will be done with the help of a nurse for
two consecutive cycles (cycles 2 and 3). Patients will then have to use to application by
themselves for the two following cycles (cycles 4 and 5)
n/a
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