Build robust digital clinical trials with real-world data using no code
All your health information in one place
Simple and free daily symptom tracker
From ingestion and aggregation of raw data, to standardization and harmonization of disparate data types
Standardize & classify healthcare codes and concepts
Uplift & transform patient data to optimize your workflow
Compute hierarchical condition category (HCC) risk adjustment profiles
Privacy-preserving record linking across data sources and use cases
Securely match patient records in 2 simple steps
Reference guides, tutorials, and tools to develop your own participant experiences with the MyDataHelps APIs and SDKs
Reference guides, tutorials, and resources for using MyDataHelps Designer
Reference guides, tutorials, and tools for using the Orchestrate APIs
Manage your developer account and explore the Orchestrate APIs
Case studies, blogs, and white papers
Journal articles from partners leveraging CareEvolution’s platform
Webinars, conferences, and product educational resources
News articles and press releases
How we protect your data
Explore examples to get an idea of what’s possible with decentralized clinical trials and research
Collect high-quality data, fast—save your time and budget
Easily incorporate EHR and claims data in patient-centric clinical trials and research.
Electronic health records (EHR) and claims provide a depth of real-world data that enhances the power of digital clinical trials and research.
In patient-centric clinical trials and research, participants can choose to share EHR and claims data, including:
Diagnoses
Medications
Labs
Observations
Family Health
Encounters
Procedures
Vitals
Notes
Utilization
Immunizations
Care Plans
The National Institutes of Health (NIH) All of Us Research Program leverages CareEvolution’s MyDataHelps™ digital clinical trial and research platform to add a “direct volunteer” participant experience for people recruited outside of a provider’s office. This allows anyone to enroll in All of Us from virtually anywhere using a white label version of the MyDataHelps™ app. Direct volunteers are able to share EHR data with the program without expensive integration with a healthcare provider organization. Where traditionally there would be no EHR data collected for these completely-virtual patients, MyDataHelps™ has enabled connections to over 1,000 distinct provider data sources. This is particularly remarkable having been achieved without requiring incentives and only through automated reminders for participants to elect to share their data.
CareEvolution’s platform can reach over 85% of all U.S. healthcare delivered annually. Connect to EHR data from over 1.5 million providers and nearly all the leading national and regional health plans. See which providers across the nation you can connect to with CareEvolution.
Data sharing is participant-mediated, which does not require a formal relationship or contract with the provider. Patients are also able to view their data in our app, thereby doubling as a personal health record.
Meet participants where they are. With multi-platform (Apple, Android, Web) capabilities, participants can share their data from their personal devices from virtually anywhere.
Participant-mediated exchange allows EHR and claims data sharing to scale easily without requiring any new contracts or relationships with the participants’ providers.
Raw data is enhanced to support research use cases through:
MyDataHelps™ is a digital clinical trial and research platform, powered by CareEvolution. Select the data and modules you need to quickly launch your next clinical trial or research project, hybrid or decentralized, with no coding required.
