Enrolling participants into a patient research registry presents unique challenges, such as obtaining IRB approval, walking users through an informed consent, and asking many personal questions. The goal of this project was to revamp ArthritisPower’s registration process to both meet all of those needs, and make it a delightful process for the user.
Inspire patients to contribute to arthritis research. Break down the informed consent into lay terms, before presenting the full document. Ensure users can register easily on mobile devices.
Communication Strategy, Custom Development, Iconography, Information Architecture, Messaging, User Experience, Website Design, Wireframing.
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