The ICC-CTN aims to undertake a program of Public and Patient Involvement and Engagement to ensure our research is patient-centred, accessible and meaningful to the public and our patients.
The ICC-CTN aims to undertake a program of Public and Patient Involvement and Engagement to ensure our research is patient-centred, accessible and meaningful to the public and our patients.
What is Public and Patient Involvement?
Public and Patient Involvement is research being carried out ‘with’ or ‘by’ members of the public and patients rather than ‘to’, ‘about’ or ‘for’ them (INVOLVE; http://www.invo.org.uk
It is active partnership between researchers and patients and/or the public.
What is Public and Patient Engagement?
Public and Patient Engagement is a two-way process of sharing knowledge and interacting with the public but does not represent active partnership.
ICC-CTN Involvement activities
Identifying what research is most important to patients and the public
Helping to design research studies & discussing types of research
Providing feedback on trial processes e.g. how consent is obtained
Reviewing patient/public-facing materials e.g. study information leaflets
Improving dissemination to the public
ICC-CTN Engagement activities
Public focus groups
Public surveys (national & international)
Public dissemination activities
The Irish Critical Care-Public and Patient Involvement group
International Public & Patient Involvement Activities