Patient centricity in clinical research is no longer optional, it is a regulatory, ethical, and operational imperative. As clinical trial technology continues to evolve, sponsors and research teams must better understand how participants experience the tools they are asked to use every day.

From eConsent to eCOA, technology choices directly influence participant engagement, compliance, and trial completion. To design clinical trials that perform under real-world conditions, industry leaders need clear insight into what patients actually want, and which friction points undermine the participant experience.

eConsent and eCOA: The Participant Point of View

This white paper explores patient perspectives on clinical trial technology, including eDiaries and informed electronic consent, and highlights the key usability challenges sponsors must address to improve retention and data quality. Download this important white paper and discover:

Are eDiaries the path forward for particpants?

Do participants prefer paper or digital for informed consent?

What clinical research leaders should tackle next to improve patient experience. 

Grounded in participant feedback, this YPrime report provides practical guidance for clinical trial sponsors looking to align clinical trial technology with participant expectations—while supporting stronger engagement and more reliable outcomes.

To learn more about YPrime eCOA and how it supports the participant experience, visit www.yprime.com/ecoa.