Recently, we at Health Affairs hosted a Twitter chat with the Patient-Centered Outcomes Research Institute (PCORI) on the topic of patients' use of evidence. The chat was a follow-up to the Health Affairs issue, “Patients' and Consumers' Use of Evidence.”
During the Twitter chat, we moderated a question-and-answer session with PCORI's Joanna Siegel, Director of Dissemination and Implementation.
Here's how PCORI describes “engagement in research.”
A2. The active involvement of patients and others in research from developing the questions to helping implement findings #patientevidence
- PCORI (@PCORI) June 17, 2016
Thanks to all those who joined the conversation! For a summary of the chat, see the Storify below. For more information on this topic, check out the archives from our issue briefing on #patientevidence.
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