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Participant EngagementY-Prime

YPrime Patient Engagement is a cloud-based solution designed to support communication, adherence, and retention of participants in clinical trials. It provides digital tools that enable reminders, notifications, and structured interactions between study teams and participants. The system operates within regulated research environments and integrates with other clinical technologies to centralize participant-related activities and improve study continuity.

Vendor

Vendor

Y-Prime

Product details

YPrime Patient Engagement is a cloud-based solution designed to support communication, adherence, and retention of participants in clinical trials. It provides digital tools that enable reminders, notifications, and structured interactions between study teams and participants. The system operates within regulated research environments and integrates with other clinical technologies to centralize participant-related activities and improve study continuity.

Key Features

Participant Communication Tools Structured digital communication between sites and participants.

  • Automated notifications
  • Visit reminders
  • Study-related announcements

Adherence Support Helps participants complete required study activities.

  • Assessment reminders
  • Dosing reminders
  • Time-based alerts

Multi-Channel Delivery Flexible communication methods.

  • Mobile device notifications
  • Provisioned device support
  • Bring-your-own-device (BYOD) compatibility

Integration with eCOA and IRT Centralized study coordination.

  • Linked assessment schedules
  • Alignment with randomization and visit plans
  • Unified participant tracking

Compliance Monitoring Oversight of participant engagement levels.

  • Completion tracking
  • Real-time adherence visibility
  • Reporting dashboards

Secure & Role-Based Access Maintains controlled study communication.

  • Site-level configuration
  • Sponsor and CRO oversight
  • Audit trail documentation

Benefits

Improved Participant Retention Supports sustained engagement throughout the study.

  • Timely reminders
  • Consistent communication

Higher Protocol Compliance Encourages completion of scheduled activities.

  • Automated prompts
  • Reduced missed visits

Operational Efficiency Reduces manual follow-up by study teams.

  • Automated workflows
  • Centralized oversight

Enhanced Data Completeness Supports timely data submission.

  • Real-time completion tracking
  • Immediate visibility into missing activities

Global Study Enablement Supports multinational trials.

  • Configurable messaging
  • Localization capabilities
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