![]() ![]() ![]() ![]() What Are The Benefits of Using ePRO In Clinical Trials?Īt ClaraHealth, the patient experience is at the very essence of our core values as a company, and incorporating ePRO software into your trial is one of the ways to design an inclusive, accessible and patient-centric clinical trial. Since patients input their findings directly in a digital format, depending on the features of the ePRO solution you pick, you and your team will be able to monitor, analyze and respond based on the data you are seeing.įor example, some ePRO solutions are able to provide you with real-time attribution, which allows you to identify and address challenges or opportunities significantly faster than with traditional paper form patient-reported outcomes. There are numerous benefits to using ePRO in clinical trials for both patients and clinicians, and this single switch to a paperless data collection process has potential to significantly improve the overall patient study experience.įurthermore, ePRO has several benefits to you as a study sponsor when it comes to processing and understanding your study data. While eCOA is the broader category which contains ePRO, many clinicians will use this term instead to refer to electronic patient-reported outcomes. This term refers to all electronically recorded outcomes, inclusive of patient-reported outcomes. In clinical trials, another common term that is associated with ePRO is eCOA, which stands for “electronic clinical outcome assessments”. What Is ePRO and How Is It Used In Clinical Trials?ĮPRO (short for electronic patient-reported outcomes) is a term that describes a category of clinical trials software which enables patients to digitally report their trial experience via their smartphone, tablet or computer, replacing the traditional approach of using paper forms. ![]()
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