eCOA/ePRO for Pediatric Clinical Trials
uMotif’s modern technology platform supports a range of pediatric studies, capturing eConsent and eCOA/ePRO for all phases of clinical and real-world research.
Learn how uMotif’s Care Cluster solution supports the needs of pediatric trials involving multiple caregivers to capture high-quality data.
Easy-to-use technology for pediatric trials
Providing user-friendly technology and keeping participants engaged, retained, and capturing ePRO and eDiary data is critical for study success.
Since 2012, uMotif has been at the forefront of designing solutions that support the clinical trial journey, leading to high levels of engagement and data capture compliance. Our tailored, configurable platform delivers an exceptional patient-centric experience to capture any ePRO/eDiary data for pediatric studies.
Attributable data from multiple caregivers — aligned around a single schedule
uMotif understands that the participant and their caregivers function best as an integrated team. Our flexible Care Cluster solution supports this vision.
It features a mobile interface that’s easy-to-use and attributes data to each caregiver for greater transparency, data quality assurance, and alignment around the patient.
Configurable data review options
In some pediatric studies, caregivers may need to view previously entered data — for example, to check if an episodic seizure, bleed, or attack has been recorded.
uMotif’s controlled, read-only access enables caregivers to view certain diary data through the app. This helps avoid duplicate data, and enhances caregiver usability.
Our user-centric approach can deliver the information in-line during a questionnaire and through a dedicated module to maximize usability.
Patient-specific symptom and event “nicknames”
uMotif’s Care Cluster solution supports remote setup and management of personalized symptom and event nicknames – making it easier for caregivers to contribute detailed data.
Nicknames are linked to medical terms by clinicians, ensuring data capture is simple for caregivers while enhancing data accuracy and quality.
The ability to nickname events is particularly important for epilepsy and seizure-related studies, including those working with the Epilepsy Consortium with seizure-type adjudication.
Insight from the field
Leverage uMotif’s deep understanding of the user journey and our expert team of scientists, solution designers, and project managers to explore how our technology can enhance data collection in pediatric clinical trials.
Read about practical data collection considerations for multi-caregiver trials in an Applied Clinical Trials article co-authored by uMotif Chief Scientific Officer Florence Mowlem, PhD.
Book a Demo
Get in touch today to discuss how we can support your pediatric clinical study.