Electronic Patient-Reported Outcomes in clinical trials refers to the use of electronic methods, such as digital devices or software applications, to collect patient-reported outcomes and data directly from study participants.
ePRO allows participants to provide self-reported information about their symptoms, quality of life, treatment satisfaction, and other relevant measures, providing valuable insights into the patient experience during a clinical trial.
Your Research has an extensive library with validated scales and is a CE-marked medical device that guides subjects personally and provides researchers with real-time insight into data for key decisions and monitoring.
Automate participant data capture
Allow participants to provide self-reported information about their symptoms, quality of life, treatment satisfaction, and other relevant measures, providing valuable insights into the patient experience during a clinical trial.
Participants are informed through personalized notifications via email, SMS, push notifications, or in-app messages.
Patient-Reported Data Collection
ePRO allows patients to directly report their symptoms, experiences, and outcomes through validated scales on electronic devices.
Real-Time Data Capture
ePRO enables immediate and accurate data capture, providing researchers with timely access to patient-reported information, enhancing data quality, and reducing the risk of data entry errors.
Remote Monitoring and Engagement
With the Your Research ePRO module, patients can conveniently participate in clinical trials from their own homes, increasing patient engagement and adherence to study protocols while minimising the need for frequent in-person visits.
Benefits and value
Enhance your research with ePRO
Enhanced accessibility supports informed decision-making, data-driven insights, and faster evaluation of treatment efficacy and safety in clinical trials.
Enhanced Patient Engagement
ePRO promotes active patient involvement by allowing them to conveniently report their experiences and outcomes in real-time, leading to improved patient engagement, compliance, and retention in clinical trials.
Accurate and Timely Data Collection
By capturing patient-reported data directly from the source, ePRO eliminates the need for data transcription, reducing errors and ensuring accurate and timely data collection, which enhances the overall data quality and reliability of clinical trial results.
Improved Data Accessibility and Analysis
The Your Research ePRO system facilitates efficient data management, organisation, and analysis, enabling researchers to access and analyse patient-reported data more easily.
Streamline your research with ePRO
Discover how our ePRO module optimises clinical trials and academic research, enhancing data collection and participant comprehension.
Integrate and customise to be compliant
- User-friendly interface is easy for patients to navigate and use.
- Designed with clear instructions and intuitive features to ensure accurate and reliable data collection.
- Support multiple languages, as needed, to accommodate diverse patient populations.
- Has robust security measures in place to protect patient data and maintain confidentiality.
- Complies with relevant regulations such as HIPAA (Health Insurance Portability and Accountability Act) in the United States or GDPR (General Data Protection Regulation) in the European Union.
- Is compatible with various devices, such as smartphones, tablets, or web browsers, to provide flexibility for patients.
- Supports different operating systems and is accessible across different platforms.
- Integrates smoothly with other clinical trial systems, such as electronic data capture (EDC) systems or electronic health record (EHR) systems, to enable efficient data collection, management, and analysis.
Along the participant journey
With Your Research, you have the flexibility to utilize stand-alone modules, integrate them with your existing software vendors, or connect them to other modules within Your Research to enhance the participant journey.