Describe the use of ePROs in longitudinal research How can ePROs be used to collect data from caregivers of patients participating in clinical trials?

The Web Site and Application will provide and collect certain information, materials and data related to clinical trial activities. PROMIS addressed a need in the clinical research community for a rigorously tested patient reported outcome (PRO) measurement tool that uses recent advances in ... Feb 7, 2018 ... based guidance on PRO-specific information that should be in- cluded in clinical trial protocols. ... ePRO Good Research Practices Task Force ... ePRO are patient-provided information about symptoms, side effects, drug timing and other questions recorded on an electronic device during a clinical trial. Oct 23, 2023 ... ... information in the informed consent process about the ... clinical trials: best practice recommendations from the ePRO consortium. ... ePRO instrument facilitated communication between patient and ... clinical trials: a patient-reported outcomes measurement information system initiative. Experienced clinical research professional with over 10 ... study specific informational guides or procedures (unique testing or constant wakefulness). Jan 9, 2024 ... The digital paradigm shift in healthcare has made it easier to collect patient information ... clinical studies, to validate ePRO. The proposed ... (eConsent), electronic patient reported outcomes (ePRO), electronic clinical outcome assessments (eCOA), and use of ... patient profiles that are more informative. Mar 25, 2020 ... Eligible patients received detailed information regarding the study and, if interested, were ... measures: ISPOR ePRO Good Research Practices Task ...