Abstract
Using bring-your-own-device (BYOD) to collect patient-reported outcomes (PRO) data is thought to improve convenience for trial participants. Seldom considered is the impact of BYOD on site workflow and activities, in comparison to using dedicated provisioned devices (PDs) provided to each participant. This qualitative study investigated the attitudes and experiences of site personnel involved in two global studies using BYOD ePRO, with an aim of understanding and alleviating potential pain points (Study 1: age 50+, Study 2: 18+).
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