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family
1,013 studies tagged family, dated 1986-10-01 to 2026-09-17 (1 undated). Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Is there a role for artificial intelligence in end-of-life care for persons with dementia? Perspectives of and recommendations by caregivers and hospice staff 2026-09-17
- Online Peer Support Use Among Informal Caregivers of People Living With Alzheimer Disease or Related Dementias: National Cross-Sectional Web-Based Survey 2026-09-07
- Interconnected Challenges in Dementia Caregiving: A Co-occurrence Network Analysis of Burden, Unmet Needs, and System Failures Among Caregivers 2026-08-17
Studies
1,013 studies carry this tag; 1,012 of them have a date.
Date range
1986 to 2026
Top journals
- Journal of the American Geriatrics Society 63
- The Gerontologist 48
- Alzheimer s & Dementia 28
- International psychogeriatrics 28
- Journal of the American Medical Directors Association 26
339 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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All hypotheses that referred to the construct validity were supported.
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There is accumulating evidence that chronic dementia caregiver stress increases their vulnerability to disease and diminishes their ability to provide optimal care.
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The decision-support intervention piloted in this study was feasible and relevant for surrogate decision-makers of persons with advanced dementia in NHs, and it improved quality of communication between SDM and NH providers.
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This German study challenged the common assumption that keeping a person with dementia at home is always cheaper than nursing home care.
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This Cochrane systematic review looked for solid evidence that respite care (temporary relief for caregivers) helps caregivers or people with dementia.
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45/100
Preexisting physician attitudes, knowledge, and beliefs prevent emergency physicians from addressing PC needs for AD patients.
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Professional caregivers may initiate ACP early if strategies carefully consider timing and family and patient receptiveness or reluctance, and are family and patient-centered.
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Approaches to palliative care that were originally developed for people with cancer are now being adopted for people with dementia, as a response to many reports of poor-quality care for people with dementia at the end of life.
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Responsibility for managing medications for older adults and/or people living with dementia in the community often falls to informal caregivers.
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Emotion-focused, patient-centered interventions like PIPAC hold promise for advancing treatment options in the early and mild stages of dementia.
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Many community-residing PWD and their caregivers have unmet dementia-related needs for care, services, and support.
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Multiple reasons contribute to the institutionalization for people with dementia, with several factors that may influence why there were country differences.
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40/100
These are not problems distinct to palliative care, but they may have different origins and explanations compared to other areas of health care.
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The aim of this study was to undertake a systematic review and narrative synthesis of the literature concerning place of death of people with dementia and the preferences for location of death of people with dementia as well as family carers and healthcare providers preferred location of death for patients with dementia.
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The concepts of compassion, kindness and humanity in dementia care are discussed within the paper.
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Our literature search resulted in 32 studies published until October 2012.
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Purpose of the study The purpose of this study was to test the impact of Function-Focused Care for the Cognitively Impaired Intervention on nursing home residents with dementia and the nursing assistants who care for them.
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To understand family members' perspectives on person- and family-centered end-of-life care provided to nursing home (NH) residents with advanced dementia, we conducted a qualitative follow-up interview with 16 respondents who had participated in an earlier prospective study, Choices, Attitudes, and Strategies for Care of Advance Dementia at End of Life (CASCADE).
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Health and social care professionals can build on people's preferences for informal planning by exploring the assumptions underlying them, providing information about the possible illness trajectory and discussing the options of care available.
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The mapping system appears useful from a nurse manager's standpoint for exploring the dementia care pathway.
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Internet interventions for informal dementia caregivers may improve caregiver well-being.
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43/100
This small non-randomized study is the first end-of-life care in dementia intervention to report an increase in family satisfaction with a reduction in hospital deaths.
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For older people living with a diagnosis of dementia, the experience of living and dying in a care home is inextricably linked.
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We have provided the first definition of palliative care in dementia based on evidence and consensus, a framework to provide guidance for clinical practice, policy and research.
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A technology-based format was feasible for delivering a multi-component intervention to minority family dementia caregivers.
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Alzheimer's disease (AD) is the most common type of dementia and is a significant public health problem that will intensify as the population ages.
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Communication regarding care is rarely patient driven and more often professional caregiver or family driven.
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Supporting family caregivers of individuals with dementia throughout the disease trajectory requires consideration of caregivers : (1) physical, emotional, and psychological needs; (2) information and decisional support needs; and (3) instrumental support needs.
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NHs appear to provide less-aggressive end-of-life care to decedents with dementia than to those without.
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In the absence of disease modifying therapies for dementia, the question rises what the benefits are of an early dementia diagnosis for patients and their caregivers.
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This article explores how married couples managed their finances and made financial decisions when one spouse had dementia, drawing comparisons with the approaches used prior to the illness.
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A lower level of nursing support managed to sustain and build on the initial outcomes.
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Awareness of the terminal nature of dementia may improve patient comfort at the end of life.
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This qualitative evaluation of ACP in early dementia has encouragingly positive results which support the wider application of the intervention in memory services and community mental health teams.
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These data indicate the high symptom burden of persons with dementia in Germany at the end of their lives.
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Regardless of the dementia stage, many nursing home residents develop serious clinical complications and symptoms in the last phase of life, posing major challenges to the provision of optimum end-of-life care.
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Preliminary results suggest that hospice enrolment might be influenced by the facility or region of this particular country.
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Further findings are organized according to the existential life worlds.
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Patients with dementia receive suboptimal palliative care, and this patient group is at risk to have pain at the end of life.
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52/100
Adjustment to admission to residential care can be difficult for people with dementia and their family caregivers.
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The booklet may help nurses educate families about end-of-life issues in dementia palliative care, but local adaptation of the booklet content and physician engagement are necessary.
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Care for the person with dementia requires understanding of the person's perspective and preferences, integrated with knowledge of dementia's trajectory and appropriate care.
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Case conferencing provides opportunities to improve care palliative care outcomes for older people with dementia by engaging family and all relevant internal and external health providers in prospective care planning.
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Although the majority of studies agreed that the Functional Assessment Staging 7c criterion was not a reliable predictor of 6-month mortality, we found a lack of prognosticator concordance across the literature.
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This study has identified the professional, organisational and legal factors that influence advance care planning implementation; professional training should target these specific areas.
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Providing artificial feeding and fluids and discussing euthanasia may be particularly sensitive topics, and guidance on these subjects needs careful consideration of ethical aspects and possible adaptations to local standards and practice.
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Wishes and preferences of people with dementia and their family carers may differ.
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Residents dying with advanced dementia who received SNF care in the last 90 days of life had fewer aggressive treatments and lower odds of hospital death if they also received hospice care at any point during that time.
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There is an extensive body of qualitative literature on the experiences of community-dwelling individuals with dementia on receiving and adapting to a diagnosis of dementia.
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The number of people with dementia is growing at an alarming rate.
From across this tag
10 of the 1,002 studies in this tag, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 10. The same 10 appear here every time.
- Emergency Department Care Coordination Program for Assisted Living Residents With Dementia
- Recommendations on end-of-life care for people with dementia
- Working with culture: a qualitative analysis of barriers to the recruitment of Chinese-American family caregivers for dementia research
- Patient and caregiver characteristics and nursing home placement in patients with dementia
- Exploring Differential Perceptions and Barriers to Advance Care Planning in Dementia among Asian Patient-Caregiver Dyads-A Mixed-Methods Study
- End-of-life care for people with dementia from ethnic minority groups: a systematic review
- An evaluation of palliative care contents in national dementia strategies in reference to the European Association for Palliative Care white paper
- End-of-life care and the effects of bereavement on family caregivers of persons with dementia
- Clinical Practice Guidelines for Dementia: Recommendations for the Pharmacological Treatment of Behavioral and Psychological Symptoms
- Using a Trauma-Informed Care Approach to Understand Family Caregivers’ Experiences of Accessing Formal Supports in Dementia Care