Explain the implications of BYOD for ePROs How is technical support provided to patients using their own devices for ePROs?

Jul 29, 2022 ... In clinical trials, the most common IoT devices are electronic Clinical Outcome Assessments (eCOA) or Patient Report Assessments (ePRO), sensors ... On the one hand, this kind of data provides valuable information from outside the idealized setting of clinical trials; on the other hand, it is problematic ... May 23, 2023 ... ... ePRO symptom monitoring between clinic visits) or no comparator depending on study design. ... No systems provided patients with general ... Mar 25, 2020 ... Eligible patients received detailed information regarding the study and, if interested, were ... measures: ISPOR ePRO Good Research Practices Task ... Nov 6, 2023 ... ... ePRO Measurement in Clinical Trials. Patient. 2015;8(4):301-309. doi ... product such as information from analytical and in vitro studies, non- ... ... study site or study country in the ePRO ... Clinical Trials: Isolate Blinded Product Information; User Help: Isolate Blinded Clinical Trial Information ... Aug 27, 2013 ... Continuous Safety Monitoring for Randomized Controlled Clinical Trials with Blinded Treatment Information ... ePRO, web-based ... ... clinical trials: best practice recommendations from the ePRO consortium. Ther Innov Regul Sci, 53 (4) (2019), pp. 431-440. Crossref View in Scopus Google ... Informed consent is a critical-to-quality (CTQ) factor for patient safety in clinical trials. ... informational document for study participants. Longer ... Jan 9, 2024 ... The digital paradigm shift in healthcare has made it easier to collect patient information ... clinical studies, to validate ePRO. The proposed ...