CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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Edge AI Is Reshaping How Clinical Trials Run
Edge computing and AI are transforming clinical trials – enabling real time monitoring, decentralized research, and faster, more cost-effective drug development.
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Telehealth In Clinical Trials: What Sites And Patients Think
Sites and patients have complicated views on telehealth in trials. Here’s what the evidence shows about who benefits, who bears the burden, and where the limits are.
ECOA RESOURCES
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Experience seamless, secure, and flexible eCOA data collection with our application designed for diverse users, compatible with multiple devices, and equipped with offline functionality and robust authentication.
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Watch YPrime's Product Director of Decentralized Trial Technology and eCOA Product Innovation Karl McEvoy discuss the utilization of user-focused research on software design and implementation.
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This presentation explores how digital health tools and AI diagnostics are transforming clinical research, driving accurate evaluations and faster therapy development for chronic pain and neurological disorders.
ECONSENT RESOURCES
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While informed consent is a critical process for ensuring participant autonomy, consent forms are too long, unclear, difficult to read, and frequently exceed 9th grade reading levels. Explore why eConsent is a potential solution to this problem.
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Clinical trials are essential to advancing medicine, yet they carry significant environmental costs. Inefficiencies not only drive emissions but also risk drug shortages and trial delays, and clinical technology solutions offer a pathway to more sustainable research.
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The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.
EPRO RESOURCES
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Patient-reported outcomes (PROs) assess patients' health without clinician interpretation. Traditional paper methods often result in missing data and quality issues, while electronic solutions enhance data accuracy and completeness.
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Patient-reported outcomes (PROs) are vital for clinical trials but can burden participants and providers. Discover strategies and practical solutions to ease these burdens and improve data quality.
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Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.