Palliative Care Studies Advisory Group
The Palliative Care Studies Advisory Group is a patient, public & lay involvement (PPI) panel who work closely with the palliative and end of life care research group, to advise on current and future research in palliative care.
The Palliative Care Studies Advisory Group (PCSAG) are a friendly group of local people who work closely with our researchers, to advise on our programme of research. The group play a crucial role in ensuring our research is relevant to patients and carers, and gives a voice to those with personal experience of palliative and end of life care.
Anyone with experience of palliative care services or hospice can join, this includes patients, their family members, friends and advocates.
The group meet in 91Ö±²¥ three to four times a year, with a hybrid option for those unable to join in person. We also regularly communicate by e-mail. Group members are reimbursed for any travel expenses and refreshments are provided at meetings.
To read more about the activities of the group you can read our Briefing Paper which describes the role of PPI in palliative care research. You can also have a look through ourwhich provides guidance and advice about PPI in palliative care research. To join the group, or have an informal chat about joining, please contact Clare Gardiner (c.gardiner@sheffield.ac.uk).
The PCSAG are committed to encouraging Equality, Diversity and Inclusion (EDI) amongst the membership and in the research they support. You can read our EDI statement here. You can also read our Terms of Reference. The PCSAG have adopted the to improve the quality and consistency of our work.