What are the different ways patients can complete ePRO assessments?

Oct 26, 2017 ... An additional section has been added in order to capture information related to the echocardiographic sub-study. 6.3 Recording of adverse events. May 15, 2023 ... The US Food and Drug Administration has made it clear that electronic capture of clinical trial source data is preferred over paper-based data ... Feb 7, 2018 ... based guidance on PRO-specific information that should be in- cluded in clinical trial protocols. ... ePRO Good Research Practices Task Force ... Sep 21, 2020 ... ... ePRO symptoms to their clinicians ... The cancer patient participants in the study were particularly interested in receiving tailored information ... treatment with improvements obtained in earlier clinical trials. A ... Paper presented at the Drug Information Association Conference on Benefits and Challenges. during a clinical trial, and provide optimal information about the patient perspective for use in making conclusions about treatment effect at the time of ... Patients entered. ePRO symptom data for their health care teams to view on the ... technology in cancer clinical trials. JCO Clin Cancer Inform. 2018;2:1-11 ... Apr 19, 2024 ... record, and the patient's ePRO data and private information were merged. ... clinical trials in oncology. J Natl. Cancer Inst. 1993, 85:365 ... ... study site or study country in the ePRO ... Clinical Trials: Isolate Blinded Product Information; User Help: Isolate Blinded Clinical Trial Information ... Jul 29, 2022 ... In clinical trials, the most common IoT devices are electronic Clinical Outcome Assessments (eCOA) or Patient Report Assessments (ePRO), sensors ...