Skip to main content

Advertisement

Table 1 Participants in phase 1a qualitative research

From: What is important to people living with dementia?: the ‘long-list’ of outcome items in the development of a core outcome set for use in the evaluation of non-pharmacological community-based health and social care interventions

Participant groups Interviews Focus groups Total Participants
People living with dementia 14 1 (n = 3) 17
Care partners 8 2 (n = 5,5) 18
Health & social care professionals 8 1 (n = 7) 15
Policy makers 4 0 4
Researchers 1 0 1
  35 20 55