The use of eCOA in oncology clinical studies is on the rise, but not without implementation challenges. Patient fatigue, questionnaire response burden and logistical complexities can all contribute to missing and incomplete data. That’s why YPrime’s eCOA solution was designed with oncology trials in mind – to minimize response burden, while providing flexibility and creative data collection solutions that promote compliance and withstand regulatory scrutiny.
Data Collection Solutions for the Unique Needs of Oncology Studies
YPrime’s eCOA platform offers features designed to simplify even your most complex oncology studies:
- Proxy entries with unique user IDs allow caregivers or site staff to enter data on behalf of the patient.
- Visit closeout features offers explanation of missed data, and allows patients to continue through the study even if they have missed a previous visit.
- Visit reactivations permit starting the visit over on a different day so data are not lost if patient is unable to complete an activated study visit.
- Site-based solutions come with the ability to share data across tablets, simplifying logistics during busy clinic days and making home-health visits easier for site staff.
YPrime’s data monitoring service combines automation and clinical expertise to ensure eCOA data collection compliance. This is especially beneficial when home-based diaries are part of your study. In addition, continuous monitoring prompts timely and appropriate intervention, when needed.