Involving the public in your study is important, especially at the research design stage, this is known as ‘Public Involvement’ or ‘Patient & Public Involvement’ (PPI). This involvement can greatly improve the quality of your study design and documentation.
To better support researchers with this process (in particular for the purposes of clinical research), there is now a dedicated space for guidance, resources and wider reading, on the Clinical Governance blog space.
You can find the page here – as always if there are any specific queries, please get in touch with Research Ethics.
Health Research Authority public involvement guidance – third blog post
NIHR resources – Patient and Public Involvement and Social Media Toolkit
Health Research Authority public involvement guidance
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