| 10 Chapter 2 undertakes an integrative literature review to explore preferences around starting a diagnostic trajectory for dementia. How can healthcare providers contribute to bridging the gap between the diagnostic phase and the post-diagnostic support phase? Chapter 3 utilizes a mixed approach that utilizes survey and interview data to gain a comprehensive understanding of how healthcare providers can support people from diagnosis to support. How do people with dementia and informal caregivers experience support and what factors are important in support satisfaction? Chapter 4 explores satisfaction with support through survey data of people with dementia and informal caregivers. How can qualitative methods support the engagement and participation of people with dementia? Chapter 5 describes and evaluates the development of a qualitative method called ‘projective techniques’. How do people with dementia and informal caregivers experience receiving a dementia diagnosis and subsequent support in Australia, Canada, the Netherlands and Poland. Chapter 6 compares and contrast experiences of a diagnosis and support across country through qualitative data. What is the relationship between informal caregiver burden and the use of social care services for a person with dementia? Chapter 7 explores the role of social care in caregiver burden through interviews with informal caregivers and social care providers.
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