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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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Why public trust matters for data enabled trials

This Health Data Research UK bite-sized video explores the importance of trust in clinical trials that use healthcare data. It explains some of the reasons why trust varies across populations and its implications for promoting inclusivity in trial participation.
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Best practice for mental health data science

DATAMIND share a co-created checklist to guide researchers on using data responsibly in mental health research.
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