Understanding different types of involvement
We have a different guidance page, if you would like to find out about research opportunities you may wish to take part in.
There are also other ways of being involved in research. A couple of these options are explained below, in case they are of interest.
Patient and Public Involvement (‘PPI’) in research
Guidance from service users, carers and members of the public is important for research. This is often referred to as ‘Patient and Public Involvement’ or ‘PPI’. PPI may involve activities like focus groups and interviews to gain valuable feedback on different topics. For instance the aims of a research study, how information is communicated, and the best way of carrying out the study within the NHS.
There is more information on the Health Authority Research website about the importance and benefits of Public Involvement.
If this is of interest then please get in touch with us.
The role of a ‘peer researcher’ – also known as ‘persons with lived experience’ and ‘survivor researchers’
Some research studies include ‘Peer researchers’. This means a person helping to create or carry out research who has personal experience of the condition being studied. The Centre for Mental Health provide a guide on this role. A peer researcher can potentially help others to better understand a condition, and how best to support participants.
If this is of interest then please get in touch with us
