Participate™ electronic patient reported outcomes (ePRO) provides a fun and easy way for patients to contribute directly to your clinical trial. With Participate ePRO, you can send friendly, “just-in-time” notifications and reminders through SMS or email. Get the data that’s fresh in your patient’s mind.
Get started with OpenClinica Participate (ePRO)
Strengthen Patient Engagement
Make it super easy for patients to have a more active role in your trial. Deploy an ePRO experience with images, video, visual analog scales and more–that will work seamlessly on any device.
Zero Friction for Your Participants
Participate ePRO removes barriers between you and your study participants. There’s no app to install and participants can use any device(s) they like (smartphones, tablets, desktops – you name it). Participants can even securely access their dashboard without having to remember a username and password. Bring your own device (BYOD), no app to download, and no password to remember–that’s zero friction.
Fully Integrated ePRO Patient Engagement Solution
No more going in and out of different systems. Participate ePRO is fully integrated with OpenClinica’s EDC, so data managers and other study designers enjoy creating the forms in one system and in one place. A single checkbox allows you to set either a clinician-based electronic case report form (eCRF) or a patient-facing ePRO form.
Enabling Greater Patient Engagement
Listen to OpenClinica’s COO, Ben Baumann, share how OpenClinica maintains participant engagement with our ePRO module, OpenClinica Participate.
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Fully Integrated ePRO Clinical DataPatient-reported data instantly becomes part of your overall study data set.
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Clinical Data Quality and Security
With Participate ePRO and OpenClinica’s powerful form capabilities, you increase data quality and speed of data acquisition.
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Compliant and Reportable ePRO
Your ePRO data is HIPAA compliant and fully auditable. A single audit trail clearly shows patient, clinician, and study team activity in a single view for easy clinical data analysis.
ePRO and clinical data,
together as one.
Patient-reported data instantly becomes part of your overall study data set.
Clinical data quality and security.
With Participate™ ePRO and OpenClinica’s powerful form capabilities, you increase data quality and speed of data acquisition.
Peace of mind.
And, your ePRO data is HIPAA compliant and fully auditable. A single audit trail clearly shows patient, clinician and study team activity in a single view.
Resources
Check out our free tools and thought leadership to learn more about clinical data management, electronic data capture, ePRO/eCOA, decentralized clinical research, and more!