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Rapid involvement of patients and the public in evidence synthesis (RIPPLES)
The NIHR (National Institute for Health and Care Research) Innovation Observatory provides a framework to support researchers to involve public members in evidence syntheses (a process to summarise available evidence) with short time frames.
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Leading with empathy
A PEDRI (Public Engagement in Data Research) webinar exploring trauma‑informed public engagement in data research, focusing on empathy, safety and sensitive conversations.
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Finding the right moments to explain data to people
Understanding Patient Data explores key moments in a person’s journey through the health system when they may be most open to learning about how data informs their care and how their data could support research.
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