How do researchers ensure patients complete ePRO assessments?

Informed consent is a critical-to-quality (CTQ) factor for patient safety in clinical trials. ... informational document for study participants. Longer ... Oct 22, 2019 ... ... information to the requesting centre. Conclusion: The PITHIA trial ... (ePRO) system. Rebecca Lewis, Elizabeth Hill, Claire Snowdon, Emma ... ... Patient surveys, quality management, quality assurance, clinical trials software / Heinz Neuwirth ... tools' ePRO solution, Patient-Reported Outcomes for ... ... patient needs, leading to improved patient engagement and more reliable trial results. As part of our unified clinical research information software, it ... Mar 9, 2023 ... ... information that will be collected via ePRO and how that information ... information related to the clinical trial to the trial participant and. Nov 1, 2024 ... Moreover, scientific societies, patient associations, cooperative groups, and institutions have their own clinical trial informational platforms ... Evaluating Risk in the Era of Decentralized Clinical Trials - By Allison ... October 25, 2023 Applied Clinical Trials SCOPE Europe 2023 Roundtable: eCOA- and ePRO ... information related to the study on any website or social media site (eg, ... ePRO Diary: Patients will be asked to use an ePRO device to record headache ... May 6, 2021 ... We assessed the feasibility of ePRO completion in older men receiving treatment for advanced prostate cancer both within the clinic and from home. Dec 14, 2023 ... ... clinical trials: best practice recommendations from the ePRO Consortium. ... information underlying the analyses and findings of a clinical ...