Abstract

There is a significant lack of evidence regarding optimum models for service provision in young onset dementia (YOD). Our study aim was to gather detailed information about services experienced as helpful by those with YOD and family carers. The objective was to identify the core features of these services to inform service design, delivery and improvements. A qualitative approach based on appreciative inquiry was used, posing open-ended questions about services experienced as helpful, as part of a national UK survey of people with YOD and carers. We used inductive thematic analysis to analyse the free-text responses. The resulting template was used as a basis for analysis of in-depth follow-up interviews, conducted to acquire greater in-depth understanding. Two hundred and thirty-three survey respondents provided 856 examples of helpful support. Twenty-four follow-up interviews were conducted (two with dyads, so 26 participants in total: 8 with people with YOD, 14 with carers, 2 with dyads). Twelve themes capturing the features of helpful services were clustered into three super-ordinate themes. 'Person-centredness' reflects micro levels of person-professional interaction (positive attitude, flexibility, collaborative, user-friendly materials, and in-person). 'Functional consistency' captures the meso level, demonstrating that services were helpful when organised consistently with needs (age-appropriate, holistic, responsive, and accessible). 'Organisational coherence', at the macro level, emphasises the need for service integration, specialist services and service continuity. Key conclusions are that the needs for flexibility and a collaborative stance may be particularly important for those under 65years with dementia, who have full lives and are used to being in control; to be age-appropriate, helpful services need to provide activities and opportunities suitable for active middle-aged people; and to be holistic, services need to provide for needs associated with rare dementias and be family-centred. Specialist services need to be commissioned and arrangements need to be stable over time to enable continuity.

Highlights

  • Young Onset Dementia (YOD) refers to dementia with onset under 65 years (Draper& Withall, 2016)

  • In the dream phase of Appreciative Inquiry (AI), we considered the themes from the perspective of their implications for YOD service provision

  • A person with YOD stated: “My strongest and most reliable professional support has come from [charity]. These are the people who have shown true concern and have remained interested in my physical and mental well-being and have been available for me to talk to.” [SP157] and a carer wrote: When my husband retired most of his friends forgot him. [ ...] [Dementia Companion] started by just going for walks with my husband, but these gradually morphed from a few hours to complete days. [...] He became his best friend and, 7 years later, still is. [...] This is the single most thing that has affected us both and I cannot stress this enough

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Summary

Introduction

Young Onset Dementia (YOD) refers to dementia with onset under 65 years (Draper& Withall, 2016). YOD is significantly different from dementia with late onset (LOD), due to the earlier stage of life and higher prevalence of rarer types (Vieira et al, 2013), resulting in distinctive needs Those with YOD need active ways to continue involvement and contribution to life; support to manage difficulties associated with vision, communication, social cognition and movement; advice on employment and finances; and support for families with young people (Chaplin & Davidson, 2016; Mayrhofer et al, 2018; Millenaar et al, 2016; Roach, Drummond, & Keady, 2016; Stamou et al, 2020a). This contributes to lower quality of life (Bakker et al, 2010; Baptista et al, 2016; Chemali et al, 2012), and potentially preventable service costs (Kandiah et al, 2016)

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