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Building public trust in routine data in clinical trials

Health Data Research UK (HDR UK) have created a 2-hour, self-paced training course that delves into why public trust is important in the context of clinical trials. Learn more about how to communicate and engage participants and the public on this topic on the HDR UK Futures platform.
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Guidelines for writing lay research summaries

University College London (UCL) have co-developed guidance for researchers on writing lay summaries. This was developed in collaboration with parents as part of their Kids’ Environment and Health Cohort (KEHC).
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How Do People Feel About the Use of Data?

This resource summarises public attitudes toward the use of patient data, based on research studies from 2010 to the present. It highlights key themes, such as support for using anonymised data for health research if there is public benefit, and concerns about industry using the data.
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