
Digital Endpoint: Redefining Data Collection in Clinical Trials
Digital endpoints enable continuous, objective, and remote patient monitoring through sensors and wearables, improving data quality and the patient experience in clinical trials.
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Digital endpoints enable continuous, objective, and remote patient monitoring through sensors and wearables, improving data quality and the patient experience in clinical trials.
Digital endpoints enable continuous, objective, and remote patient monitoring through sensors and wearables, improving data quality and the patient experience in clinical trials.
Reflecting on 2023, this CEO message highlights Replior’s achievements, lessons learned, and steps taken to prepare for future growth and innovation in clinical trials.
SMS notifications in ePRO systems enhance clinical trial compliance by providing immediate, user-friendly reminders, leading to higher engagement and timely data submissions.
Explore the roles of eCOA and ePRO in clinical trials, focusing on their impact on data collection, patient engagement, and patient-centric research.
Device provisioning ensures clinical trial participants have the devices they need, improving data collection, compliance, and inclusivity.
Improving patient engagement in clinical trials increases retention and data quality through ePRO systems, gamification, and tailored notifications.
ePRO systems gather patient-reported data electronically, supporting engagement, compliance, and high-quality outcomes in patient-centric clinical trials.
Trial Online ePRO drives patient engagement in clinical trials with gamification features like notifications, awards, and progress tracking, improving retention and data quality.
Patient dropouts are a major challenge in clinical trials. Addressing burdens like costs and travel with patient-centric designs and engaging ePRO tools can improve retention.