Today, ObvioHealth addressed ePRO technologies and their demonstrated ability to provide superior data. Capturing and analyzing patient-reported outcomes is essential for patient-centeredness in healthcare research and delivery. However, the life sciences sector has historically failed to collect sufficient, high-quality data from clinical trial participants, resulting in significant delays for research teams.
The introduction of decentralized clinical trials overcomes these obstacles directly via the use of electronic patient-reported outcomes (ePRO). Effective ePRO systems enable sponsors to collect high-quality data from participants in real-time, enabling them to precisely evaluate the effects of medicine on patients.
Within a decentralized or hybrid clinical trial, research teams may use strategies from the technology sector, such as enhancing the user experience and user interface in order to provide data that truly represent the lived experiences of participants.
Traditional research design often emphasizes the “ideal” data collection scenarios of the study team. In contrast, best-in-class ePRO solutions prioritize patients via human-centered design.
Human-centered design recognises that, despite the fact that participants want the research to succeed, the majority of them are very busy. Sponsors may set up participants for success by meeting them where they are and making study assignments as straightforward and easy as possible.
The simplification of data gathering with ePRO benefits both sponsors and patients. Let’s look at four ways in which ePRO decreases participant burden and provides more accurate data.
One of the most widespread misconceptions about ePRO is that it just digitizes the identical research activities that would be included in a site-based trial. For successful ePRO, however, teams must optimize surveys within a digital setting that helps patients at home.
A questionnaire, for example, may make scales more interactive, visible, and user-friendly. It may also highlight instantly if the patient fails to submit a needed answer. Again, a well-designed user interface assists users in comprehending their tasks without being confused or overloaded.
ePRO optimization also considers digital parameters. Discrepancies in the presentation of surveys on an iPhone and an Android, for instance, might influence participant responses, which can also affect the quality of the data. Experienced ePRO providers preserve data integrity with responsive design scales that seem the same on numerous devices, regardless of screen size.
Virtual research organizations (VROs) may assist sponsors in standardizing research questions and formatting prior to participants seeing them on-screen. With a variety of clinically certified ePRO solutions on the market, data collection and interpretation teams must choose the appropriate ePRO scale for the study’s unique requirements.
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