Abstract

In a theory-driven, qualitative, multiple-case study, we examined the implementation of national dementia plans (NDPs) in Denmark, Germany, and Italy to determine how stakeholders involved in implementing the NDPs evaluate contextual factors in light of the World Health Organization’s seven action areas of dementia-focused policy. To analyse the NDPs, we used a driver diagram of large-scale change and conducted both document analysis and semi-structured interviews, after which we performed three-way open coding to analyse the methods. The results show that the implementation of NDPs has increased awareness of dementia in all three countries by positioning the disease as a national public health concern. The study also reveals that resources, the use of change theory, and the monitoring of implementation and fragmentation are crucial factors to consider for countries when implementing NDPs. Although stakeholders find the NDPs useful, many challenges remain for their successful implementation due to the highly limited means for implementation and evaluation. Moreover, present NDPs all lack a communication plan that encompasses all layers of society to address ways of achieving change. Patients with dementia, and their informal caregivers, should be included more in the design, implementation, and evaluation of NDPs in order to improve their usefulness and effectiveness.

Highlights

  • As populations around the world continue ageing, the number of people living with noncommunicable diseases, such as dementia, has risen [1]

  • Our findings demonstrate the influence of certain factors on the context and process of implementing national dementia plans (NDPs) according to different stakeholders

  • Such knowledge is pivotal to improving the implementation of NDPs and ensuring proper dementia care

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Summary

Introduction

As populations around the world continue ageing, the number of people living with noncommunicable diseases, such as dementia, has risen [1]. Dementia can impact informal caregivers, including spouses, adult children, children-in-law, and/or friends, and poses a range of physical, psychological, social, and economic consequences for them and society at large [3]. Many such consequences are exacerbated by a lack of awareness and understanding of dementia, which can intensify the stigma of the disease and its patients, as well as raise hurdles for its diagnosis and care [1]. As the number of people with dementia rises, so do the costs of care and support

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