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Patient & Public Involvement & Engagement

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