Presented by William Cragg ( Regulatory and Governance Affairs Manager & Methodology Lead for Trial Conduct, University of Leeds)
Layering participant information involves dividing it up into 'key information' that all participants are asked to read before they decide about taking part in a trial, and 'optional information' that they can look at if they want to, before consent or later. Layering information could help reduce the information burden on potential participants, and give them more control about what information they decide to read. However, it can mean people can give consent without reading any of the optional information, so we need to get the layering right. There isn't a single, agreed way of doing this.
In this presentation, William will share some ideas from the Clinical Trials Research Unit at the University of Leeds on how participant information might be layered in a standardised, principle-based way, and discuss some successes and challenges with the approach so far.
This webinar will be recorded, if you are unable to attend. You will be able to access the recording via the UKTMN website Resources page, and we will notify all members as soon as this is available.
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