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Software for Administering the National Cancer Institute’s Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events: Usability Study

Software for Administering the National Cancer Institute’s Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events: Usability Study

The key functionalities were derived from an iterative process, including patients, clinical trialists, administrators, NCI, and Food and Drug Administration stakeholders, and included the following: Professional (clinician and research associate) interface: This includes a form builder that enables selection of PRO-CTCAE items and a configurable alert system that activates emails if patients miss a scheduled self-report or patients self-report a severe or worsening AE.

Martin W Schoen, Ethan Basch, Lori L Hudson, Arlene E Chung, Tito R Mendoza, Sandra A Mitchell, Diane St. Germain, Paul Baumgartner, Laura Sit, Lauren J Rogak, Marwan Shouery, Eve Shalley, Bryce B Reeve, Maria R Fawzy, Nrupen A Bhavsar, Charles Cleeland, Deborah Schrag, Amylou C Dueck, Amy P Abernethy

JMIR Hum Factors 2018;5(3):e10070