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ABSTRACT: Objectives
As part of a wider study, our aim was to elicit perspectives of people with congenital heart disease (CHD) and/or their parents/carers about their experiences of healthcare and what is important to them when receiving care.Design and setting
A qualitative study involving a series of closed, asynchronous, online discussion forums underpinned by an interpretivist framework and set up and moderated by three patient charities via their Facebook pages.Participants
People with CHD and parents/carers of people with CHD from the UK.Results
Five forums were run for 12-24 weeks across the three charities, and 343 participants signed up to the forums. Four linked themes related to processes of care were identified following thematic analysis of the transcrip
SUBMITTER: Wray J
PROVIDER: S-EPMC11218017 | biostudies-literature | 2024 Jul
REPOSITORIES: biostudies-literature