All Stories

  1. Professionals' Views on Social Care Planning and Provision for People With Young‐Onset Dementia and Their Families in England: Findings From the DYNAMIC Study
  2. Continuity, change and ‘living well’ for older people with dementia: longitudinal qualitative findings from the IDEAL cohort study
  3. Negotiating the caring role and carer identity over time: ‘living well’ and the longitudinal narratives of family members of people with dementia from the IDEAL cohort
  4. Qualitative evaluation of My Life Today - A co-produced personal tool from the IDEAL programme to help people with dementia monitor valued aspects of their lives
  5. The dementia–nature–inclusivity nexus and the needs of people living with dementia
  6. Navigating the COVID-19 pandemic two years on: experiences of carers of people with dementia from the British IDEAL cohort
  7. Emotional Labor in Dementia Research
  8. Understanding dementia in minority ethnic communities: The perspectives of key stakeholders interviewed as part of the IDEAL programme
  9. Identifying predictors of transition to a care home for people with dementia: findings from the IDEAL programme
  10. Embodied leisure experiences of nature-based activities for people living with dementia
  11. Differences in trajectories of quality of life according to type of dementia: 6-year longitudinal findings from the IDEAL programme
  12. Longitudinal Trajectories of Stress and Positive Aspects of Dementia Caregiving: Findings From the IDEAL Programme
  13. Health conditions in spousal caregivers of people with dementia and their relationships with stress, caregiving experiences, and social networks: longitudinal findings from the IDEAL programme
  14. Social care planning and provision for people with young onset dementia and their families: Protocol for the DYNAMIC study
  15. Dyadic perspectives on loneliness and social isolation among people with dementia and spousal carers: findings from the IDEAL programme
  16. Methods and approaches to facilitate inclusion of the views, perspectives and preferences of people with moderate‐to‐severe dementia in research: A narrative systematic review
  17. Resilience in caregivers of people with mild-to-moderate dementia: findings from the IDEAL cohort
  18. Provision of Outdoor Nature-Based Activity for Older People with Cognitive Impairment: A Scoping Review from the ENLIVEN Project
  19. Evaluating ‘living well’ with mild-to-moderate dementia: Co-production and validation of the IDEAL My Life Questionnaire
  20. Navigating the coronavirus pandemic 2 years on: Experiences of people with dementia from the British IDEAL cohort
  21. Provision of outdoor nature-based activity for older people with cognitive impairment: protocol for a scoping review from the ENLIVEN project
  22. Exploration of meaning, motivation, and preparedness to care amongst the one‐child policy generation in China
  23. Living with dementia during the COVID-19 pandemic: insights into identity from the IDEAL cohort
  24. Intersections between the culture of Xiao (孝) and caring for older relatives in China: perspectives of United Kingdom-based Chinese students on future care for their parents
  25. Profiles of social, cultural, and economic capital as longitudinal predictors of stress, positive experiences of caring, and depression among spousal carers of people with dementia
  26. “Living Well” Trajectories Among Family Caregivers of People With Mild-to-Moderate Dementia in the IDEAL Cohort
  27. Positive experiences in dementia care-giving: findings from the IDEAL programme
  28. Effects of social restrictions on people with dementia and carers during the pre‐vaccine phase of the COVID ‐19 pandemic: Experiences of IDEAL cohort participants
  29. Psychological processes in adapting to dementia: Illness representations among the IDEAL cohort.
  30. Interventions for self-management of medicines for community-dwelling people with dementia and mild cognitive impairment and their family carers: a systematic review
  31. Impact of COVID‐19 on carers of people with dementia in the community: Findings from the British IDEAL cohort
  32. 'Caring beyond capacity' during the coronavirus pandemic: the experiences of family caregivers of people with dementia from the IDEAL cohort
  33. The Use and Costs of Paid and Unpaid Care for People with Dementia: Longitudinal Findings from the IDEAL Cohort
  34. A comparison of well-being of carers of people with dementia and their ability to manage before and during the COVID-19 pandemic: findings from the IDEAL study
  35. Impact of COVID-19 on carers of people with dementia in the community: Findings from the IDEAL cohort
  36. Effects of social restrictions on people with dementia and carers during the pre-vaccine phase of the COVID-19 pandemic: experiences of IDEAL cohort participants
  37. Longitudinal Trajectories of Quality of Life Among People With Mild-to-Moderate Dementia: A Latent Growth Model Approach With IDEAL Cohort Study Data
  38. Limited receipt of support services among people with mild‐to‐moderate dementia: findings from the IDEAL cohort
  39. Impact of COVID-19 on ‘Living Well’ with Mild-to-Moderate Dementia in the Community: Findings from the IDEAL Cohort
  40. Living with dementia under COVID-19 restrictions: coping and support needs among people with dementia and carers from the IDEAL cohort
  41. Living with dementia under COVID-19 restrictions: coping and support needs among people with dementia and carers from the IDEAL cohort
  42. Community Ageing Research 75+ (CARE75+) REMOTE study: a remote model of recruitment and assessment of the health, well-being and social circumstances of older people
  43. Living well with dementia: What is possible and how to promote it
  44. Developing supportive local communities: Perspectives from people with dementia and caregivers participating in the IDEAL programme
  45. Psychological and Social Factors Associated with Coexisting Frailty and Cognitive Impairment: A Systematic Review
  46. Does awareness of condition help people with mild-to-moderate dementia to live well? Findings from the IDEAL programme
  47. The role of subjective social status in living well for carers of people with dementia: findings from the Improving the experience of Dementia and Enhancing Active Life programme
  48. Stressors and coping mechanisms of family care-givers of older relatives living with long-term conditions in mainland China: a scoping review of the evidence
  49. Relationship between self-perceptions of aging and ‘living well’ among people with mild-to-moderate dementia: Findings from the ideal programme
  50. Perceived and objective availability of green and blue spaces and quality of life in people with dementia: results from the IDEAL programme
  51. Loneliness and isolation among people with dementia and their carers: Prevalence, risk factors and a dyadic analysis
  52. Living Alone with Mild-To-Moderate Dementia: Findings from the IDEAL Cohort
  53. The prevalence and predictors of loneliness in caregivers of people with dementia: findings from the IDEAL programme
  54. Factors associated with self- and informant ratings of quality of life, well-being and life satisfaction in people with mild-to-moderate dementia: results from the Improving the experience of Dementia and Enhancing Active Life programme
  55. Self-esteem, self-efficacy, and optimism as psychological resources among caregivers of people with dementia: findings from the IDEAL study
  56. The impact of relationship quality on life satisfaction and well-being in dementia caregiving dyads: findings from the IDEAL study
  57. The relationship between perceived functional difficulties and the ability to live well with mild‐to‐moderate dementia: Findings from the IDEAL programme
  58. Caregiver influences on ‘living well’ for people with dementia: Findings from the IDEAL study
  59. Caregivers’ beliefs about dementia: findings from the IDEAL study
  60. Psychological predictors of ‘living well’ with dementia: findings from the IDEAL study
  61. Influence of Positive and Negative Dimensions of Dementia Caregiving onCaregiver Well-Being and SatisfactionWith Life: Findings From theIDEAL Study
  62. A Comprehensive Model of Factors Associated With Subjective Perceptions of “Living Well” With Dementia
  63. A Comprehensive Model of Factors Associated With Capability to “Live Well” for Family Caregivers of People Living With Mild-to-Moderate Dementia
  64. Use and costs of services and unpaid care for people with mild‐to‐moderate dementia: Baseline results from the IDEAL cohort study
  65. Influence of Positive Aspects of Dementia Caregiving on Caregivers’ Well-Being: A Systematic Review
  66. The impact of co-morbidity on the quality of life of people with dementia: findings from the IDEAL study
  67. Protocol for the IDEAL-2 longitudinal study: following the experiences of people with dementia and their primary carers to understand what contributes to living well with dementia and enhances active life
  68. Reflections on PPI from the ‘Action on Living Well: Asking You’ advisory network of people with dementia and carers as part of the IDEAL study
  69. Inequalities in living well with dementia-The impact of deprivation on well-being, quality of life and life satisfaction: Results from the improving the experience of dementia and enhancing active life study
  70. Beliefs About Dementia: Development and Validation of the Representations and Adjustment to Dementia Index (RADIX)
  71. Living well with dementia: a systematic review and correlational meta-analysis of factors associated with quality of life, well-being and life satisfaction in people with dementia
  72. Dualities of dementia illness narratives and their role in a narrative economy
  73. Conducting Interviews With People With Dementia and Their Caregivers
  74. Social Support and Attitudes to Aging in Later Life
  75. A Review of Self-Management Interventions for People With Dementia and Mild Cognitive Impairment
  76. Executive control in older Welsh monolinguals and bilinguals
  77. Current Practice in the Referral of Individuals with Suspected Dementia for Neuroimaging by General Practitioners in Ireland and Wales
  78. “I Don’t Think Of It As An Illness”: Illness Representations in Mild to Moderate Dementia
  79. Illness representations in caregivers of people with dementia
  80. A pilot randomized controlled trial of a self-management group intervention for people with early-stage dementia (The SMART study)
  81. Is cognitive lifestyle associated with depressive thoughts and self-reported depressive symptoms in later life?
  82. Does cognitive reserve moderate the association between mood and cognition? A systematic review
  83. A systematic narrative review of support groups for people with dementia
  84. Care staff and family member perspectives on quality of life in people with very severe dementia in long-term care: a cross-sectional study
  85. Improving the experience of dementia and enhancing active life - living well with dementia: study protocol for the IDEAL study
  86. Bilingualism, executive control, and age at diagnosis among people with early-stage Alzheimer's disease in Wales
  87. How does cognitive reserve impact on the relationships between mood, rumination, and cognitive function in later life?
  88. Help Yourself
  89. Self-management in early-stage dementia: a pilot randomised controlled trial of the efficacy and cost-effectiveness of a self-management group intervention (the SMART study)
  90. ‘It's in the eyes’: how family members and care staff understand awareness in people with severe dementia
  91. Balancing needs: The role of motivations, meanings and relationship dynamics in the experience of informal caregivers of people with dementia
  92. AwareCare: a pilot randomized controlled trial of an awareness-based staff training intervention to improve quality of life for residents with severe dementia in long-term care settings
  93. The impact of relationships, motivations, and meanings on dementia caregiving outcomes
  94. Negotiating the balance: The triadic relationship between spousal caregivers, people with dementia and Admiral Nurses
  95. What predicts whether caregivers of people with dementia find meaning in their role?
  96. AwareCare: Development and validation of an observational measure of awareness in people with severe dementia
  97. The impact of motivations and meanings on the wellbeing of caregivers of people with dementia: a systematic review
  98. The impact of the quality of relationship on the experiences and wellbeing of caregivers of people with dementia: A systematic review
  99. The experience of providing care in the early stages of dementia: An interpretative phenomenological analysis
  100. Information and support interventions for informal caregivers of people with dementia