Are there any guidelines or regulations for ePROs?

Oct 22, 2019 ... ... information to the requesting centre. Conclusion: The PITHIA trial ... (ePRO) system. Rebecca Lewis, Elizabeth Hill, Claire Snowdon, Emma ... Aug 28, 2023 ... Consent to Participate: Informed consent was obtained from all individual participants included in the study. Copyright information. © 2023 The ... Jul 29, 2022 ... In clinical trials, the most common IoT devices are electronic Clinical Outcome Assessments (eCOA) or Patient Report Assessments (ePRO), sensors ... More information about research is available on the CenterWatch website: https://www.centerwatch.com/clinical-trials/overview. What is the consent form ... Studies in cancer suggest that ePROM symptom monitoring may be associated with enhanced patient ... All study information will be archived in the BEAR ... May 17, 2023 ... Asking which decentralized elements they use in their trials so far, 43% of the participants from trial sponsors and CROs said “ePRO“, while 37% ... Objectives The Patient-Reported Outcomes Measurement Information ... Our data indicate that the integration of ePRO into oncological clinical research and ... Experienced clinical research professional with over 10 ... study specific informational guides or procedures (unique testing or constant wakefulness). Sep 21, 2020 ... ... ePRO symptoms to their clinicians ... The cancer patient participants in the study were particularly interested in receiving tailored information ... IRT (IWRS, eDiary, ePRO) ... The contents available on the Everest Clinical Research Corporation website www.ecrscorp.com are intended for informational purposes ...