Revolutionizing Pediatric Clinical Trials: Optimizing ePRO And eConsent For Enhanced Data Quality And Participant Experience

Pediatric clinical trials face unique challenges due to participants' diverse age ranges and family involvement, impacting retention and data quality. Digital tools like electronic Patient-Reported Outcomes (ePRO) and electronic Consent (eConsent) are essential in addressing these challenges, requiring a balance between regulatory compliance and user experience. Innovative solutions from companies such as Curebase focus on enhancing engagement and data accuracy through user-centric onboarding, adaptive consent workflows, and personalized notification systems. These solutions aim to create consumer-grade experiences with intuitive interfaces that mimic popular apps, making them accessible for both participants and families.