Making Data Central to Your CNS and Pain Trials

Data capture for CNS and pain clinical trials is challenging: Complicated eligibility criteria, extensive monitoring requirements, comprehensive data collection, and substantial demands on patients must be overcome. 

Resultant efficiency and real-time data availability make eSource data capture technologies particularly suitable for streamlining site requirements and shortening study timelines in exacting CNS and pain trials. Surveillance dashboards allow constant monitoring of diary data, eligibility, and safety.

Protocol-driven and study-specific implementation of a CNS-oriented eSource technology platform facilitates proper trial execution by both sites and patients.

  • Electronic clinical outcome assessments (eCOA) present structured diagnostic interviews with standard CNS questionnaires, eligibility requirements, and edit checks
  • Versatile capabilities — such as incorporation of video — simplify remote monitoring and oversight
  • Electronic patient-reported outcome (ePRO) screens for complex assessments such as rescue medication workflows are supported by dynamic response diaries that improve compliance via real-time adaptive reminders
  • User-friendly options such as BYOD (patient uses own phone) also ensures strong patient engagement

These functionalities, backed by expert, consultative guidance, are a robust solution for ePRO/eCOA and direct data capture that supports proper protocol execution and helps patients adhere to demanding CNS protocols.


 

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