Replior eCOA/ePRO
Behavioral science driven eCOA/ePRO
Most eCOA/ePRO systems solved the paper problem. They never solved the motivation problem. As studies become longer and more demanding, participant engagement naturally declines – leading to avoidable dropout, missing data, and reduced statistical power.
Replior eCOA/ePRO combines two unique components: a proprietary behavioral doctrine for designing participant engagement throughout a study, and a platform that puts those principles into practice through intelligent engagement mechanics. Together they help improve adherence, retention, and data quality, with demonstrated retention of 99% at Week 28 versus an industry benchmark of approximately 80%.
What makes our eCOA/ePRO unique
This is not just another eCOA/ePRO solution.
Replior eCOA/ePRO is built around a fundamentally different philosophy. Rather than simply digitizing questionnaires, it actively helps maintain participant motivation throughout the study.
The doctrine surfaces the participant’s altruistic intent to contribute. The system sustains it. Week after week the platform delivers those experiences automatically through personalized reminders, progress tracking, milestones and adaptive content.
The outcomes are measured, repeatable, and especially strong where commodity ePRO routinely fails.
Behavioral engagement mechanics
Every engagement feature is designed with one objective: helping participants stay engaged throughout demanding clinical trials. Visible progress builds investment that grows harder to walk away from. Milestones reconnect participants to their contribution. Messaging is calibrated to where the participant is in the protocol, not to a generic schedule.
Rather than relying on generic reminders, Replior adapts communication, celebrates progress and reinforces each participant’s contribution to the study.
Trophies, Badges and Milestones
Medals and badges mark passed milestones and completed activities, making accumulated investment tangible. The longer a participant has contributed, the more they stand to forfeit by disengaging.
Progress Tracking
Participants see time invested, tasks completed, milestones reached, and streaks maintained. Surfacing this data continuously is the mechanic that turns participation from effort into routine.
Smart Reminders
Study-specific messages calibrated to protocol milestones: onboarding, first weeks, mid-study fatigue points, dose-escalation phases, end-of-study. Push, email, and SMS. Hundreds of messages designed per study, not a generic reminder schedule.
Adaptive Video Content
Study-tailored video tracks for both low-compliance and high-compliance participants. Dedicated videos explain to lower-compliance participants what their participation means for the patient community. High-compliance participants receive recognition that affirms and reinforces the behaviour.
Diego Herrera Egea
Director of Clinical Data & Digital Innovation Almirall
Intuitive User Experience
Designed for All Age Groups
Intuitive app helps participants perform the tasks expected from them.
Customizable Widgets
Tailor the app with widgets specific to your trial needs, such as a welcome video.
Native App
Available on iOS and Android or accessible from any web browsers.
Device Independence
Support for patients using their own smartphone or provisioned devices.
Multi-language Support
Accommodate over 40 languages, with additional languages available upon request.
Unique Voice Recording
Allow patients to use voice recordings as cognitive memory notes enhancing data accuracy.
High-Quality Data Collection
Capture higher-quality data while reducing participant burden through seamless digital endpoint integration, automated data collection and real-time insights.
Real-time Data Capture
Capture timely and accurate data with questionnaires and event scheduling.
Digital Endpoint Integration
Collect data from RaySense, ScratchSense, and other connected devices automatically.
Sophisticated Scoring
Automatically score questionnaires for instant feedback and actionable insights.
Advanced Calculations
Provide precise, customizable data analysis tailored for your study with JavaScript-based calculations.
Seamless API Integration
Connect easily with EDC systems and other study-specific vendor systems to streamline data workflows.
Simple Participant Management
eConsent Integration
Simplify the consent process, ensuring compliance and easing participant onboarding.
Participant Grouping
Tailor events and questionnaires to specific groups, improving relevance and compliance.
Treatment Schedules
Provide comprehensive information and customizable schedules to ensure protocol adherence.
Logbooks and Diaries
Collect periodic or ad hoc data such as medication intake and blood pressure.
Tasks and Visits Management
Provide one-click access to tasks, visit schedules, and preparation instructions.
Management and Reporting Tools
Study Dashboard
Gain real-time visibility into study performance. Identify trends and behavior patterns.
Multiple Export Options
Easily extract data, including audit logs, notifications, and questionnaire exports.
Customizable and Standard Reports
Generate reports tailored for your needs or choose from a range of standard options.
Complete Audit Trail
Maintain a comprehensive audit trail from data entry through all changes.
Monitor Compliance, Act Early
Access insights at the study, task, site, and participant levels, allowing early action on outliers at every stage.
Where it pays off most
The behavioral doctrine produces the largest retention delta exactly where commodity ePRO fails hardest: when motivation is most tested.
52-week+ protocols:
Where motivation decay is structural and reminder-based engagement collapses
High recall-bias risk:
Where subjective outcomes drive primary endpoints and engagement quality directly shapes data quality
Dose escalation and up-titration:
Where peak side effects meet peak uncertainty and the participant most needs a reason to stay
Phase III where Phase II flagged retention risk
The highest-cost moment to discover the same problem twice
Chronic, fluctuating conditions:
Where symptom variability reads to the participant as 'it isn't working'
Prevention and healthy-volunteer trials (vaccine, contraception, PrEP):
Where participants feel fine and the industry default is monetary compensation
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FAQ
What is the average time to implement and deploy Replior eCOA/ePRO?
Is Replior eCOA/ePRO compliant with regulatory requirements?
How does Replior eCOA/ePRO integrate with other clinical trial software?
Can Replior eCOA/ePRO be customized to meet specific study requirements?
What devices are compatible with Replior eCOA/ePRO?
Does Replior eCOA/ePRO support multi-language capabilities for global studies?
Western and Northern European Languages:
- English (UK)
- Spanish
- German
- German (Austria)
- German (Switzerland)
- French
- French (Switzerland)
- Belgian French
- French (Italy)
- Portuguese
- Italian
- Dutch
- Flemish
- Swedish
- Danish
- Norwegian
- Finnish
North American Languages:
- English (US)
- Spanish (US)
Eastern and Central European Languages:
- Czech
- Hungarian
- Polish
- Romanian
- Russian
- Ukrainian
South and Southeast Asian Languages:
- Hindi
- Marathi
- Gujarati
- Bengali
- Telugu
- Tamil
- Kannada
- Malayalam
- Malay
- Chinese
Additional languages can be added upon request, making it suitable for global clinical trials so participants can interact in their preferred language.
How user-friendly is Replior eCOA/ePRO for both researchers and participants?
How does Replior eCOA/ePRO handle data from wearable technology or remote monitoring devices?
What makes Replior eCOA/ePRO different from standard eCOA/ePRO systems?
Ready to improve participant retention?