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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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The results of the extended model show that social influence, effort expectancy, facilitating conditions, and behavioral intention (BI) all had P P value for RC and TA was greater than .05, hence were insignificant.
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Our review suggests that MNPIs may improve the global, executive function and memory of PWD in NHs.
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At baseline, there were no statistically significant differences in demographic characteristics and in outcome variables (HHI, GSES, and SF-12v2 mental component score and physical component score) between users and nonusers.
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Providing peer-support groups using telehealth may have the potential to develop self-sustaining peer networks for isolated caregivers of people with dementia.
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60/100
Fifty-three studies were included in the narrative synthesis.
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Three themes emerged from 29 included studies: self-care needs and behaviors of ICGs, barriers to performing self-care, and enablers of self-care.
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Experiences translated into four themes: acknowledging human dignity; being recognised as an important caregiver; (not) talking about death and dying and making decisions together.
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All 23 were able to articulate their end-of-life wishes very or somewhat coherently during the SPIRIT session; of those, 14 PWDs had moderate dementia.
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The final cohort included 27 243 nursing home residents with advanced dementia (19 363 [71.1%] women) who died between June 1, 2010, and March 31, 2015, at the median (interquartile range) age of 88 (83-92) years.
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Thirty-five studies were analyzed with data from 3268 caregivers (pooled mean age [SD of sample means], 63.48 [5.99] years; 76.7% female) were analyzed.
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Most care staff for long-term care residents with dementia experience low or moderate burnout levels.
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At year 1, persons with ADRD improved on all scales, except MMSE and functional status measures; caregivers improved on all scales.
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A gap of knowledge, of information and in care intertwiningly hinder advance care planning.
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Educational programs may be useful in reducing racial differences in attitudes towards ACP.
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A deep learning algorithm based on patient demographic information and longitudinal clinical notes appeared to show promising results in predicting mortality among patients with dementia in different time frames.
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Research is needed with methodologically rigorous designs and theoretical frameworks that examine cognitive, psychosocial, and environmental factors influencing ACP attitudes, preferences, and behaviors among PWDs in order to improve engagement among this population.
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53/100
With the rising dementia population, more and more programs have been developed to help caregivers deal with the care-recipient as well as their own frustrations.
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A total of 41 articles met the eligibility criteria.
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41/100
Study results emphasize the need for improved EOL counseling in DLB, recognition of EOL symptoms, earlier hospice involvement, tailoring EOL care to DLB-specific needs, and clinician-family communication.
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There is an urgent need for greater consideration of the ethical and legal implications that remote technological monitoring might have upon workforce morale, recruitment and retention.
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Overall, symptoms in the last week and month of life did not vary by diagnosis.
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69/100
The review highlights the paucity of high-quality dementia-specific research in this area and recommends key areas for future work, for example, the need for process evaluation to identify facilitators and barriers to implementing interventions.
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Little is known about preferred place of death, or the factors associated with achieving this, for people with dementia.
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Healthcare providers identified caregivers in most of the sample, but less than 50% assessed their well-being and needs.
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Even though the provision of PC was empirically recognised as a care step in the management of dementia, there are barriers that hinder access of patients with dementia to appropriate facilities.
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Benefit-finding reduces depressive symptoms as well as global burden in the long-term and increases psychological well-being in the medium-term.
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In January, the NHS presented its long-awaited plan to transform care over the next 10 years.
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The process of advance care planning in dementia is far from straightforward; as dementia progresses, the ability to consider future thoughts and actions becomes compromised, thus affecting decision-making abilities.
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Families' reports of unpleasant experiences with end-of-life care may inform practice to improve perceived quality of dying of their loved ones.
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Reliable population estimates of life expectancy with dementia are required for shaping health-care policy.
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Enrollees in a comprehensive dementia care comanagement program had high engagement in advance care planning, high rates of hospice use, and low acute care utilization near the end of life.
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Of the 15 articles that were included, most used qualitative methods (N = 13) and were conducted in long-term care facilities (N = 14).
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Opioid use was significantly higher in females and Whites and varied by states.
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However, even though neurodegenerative dementia results in the gradual loss of decision-making capacity, ACP is still extremely rare.
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The role of NPT has been largely explored in AD and dementia.
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Technology-based interventions have the potential to support informal caregivers of PWD.
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This study aims to systematically evaluate the efficacy of Pet robot intervention (PRI) for people with dementia.
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Despite the increasing prevalence, growing costs, and high mortality of dementia in older adults in the U.S., little is known about the course of these diseases and what care dementia patients receive in their final years of life.
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Most importantly attributes included (1) knowing and recognizing the symptoms of decline in dementia and what dying looks like; (2) understanding emotions and grief responses; (3) accessing and appraising supports needed to manage and care for dying; (4) organizing affairs and completing tasks in advance; (5) accepting that losses are inevitable and imminent; (6) reflecting on caregiving and finding meaning, "a silver-lining"; and (7) closing, reconciling, and renewing relationship bonds and completing the family member's life.
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Five hundred and forty five patients from 67 NH units were included and randomized to the intervention ( N = 297; 36 units) and control group ( N = 248; 31 units).
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This unique study has confirmed the relevance of much of the content of existing end of life frameworks to dementia.
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The importance of better care integration is emphasized in many national dementia plans.
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51/100
Caregiver characteristics and provision of caregiving tasks determine caregiver burden more than care recipient characteristics.
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Purpose of study To assess trends in family caregiving between 1999 and 2015.
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Specialty palliative care consultation for hospitalized patients with late-stage dementia is feasible and promising to improve decision-making and some treatment outcomes.
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Quality of life of people with advanced dementia living in nursing homes is often suboptimal.
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This is the first study to test community-based family dementia caregiver intervention in Vietnam.
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Better alignment between preferences for comfort-focused care and advance directives is needed in advanced dementia.
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The findings indicate that healthcare professionals experienced several structural barriers that prevented the provision of palliative care to people with severe dementia in long-term care facilities.
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ACP is facilitated by an open relationship based on trust between the GP, the person with dementia and his/her family caregiver, in which both medical and non-medical issues are addressed.
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.
- Access to hospice programs in end-stage dementia: a national survey of hospice programs
- Criteria for enrolling dementia patients in hospice
- Communicating palliative hope in late-stage dementia: thematic analysis of hope work in care plan meetings with nursing home residents’ families
- Predictors of caregiver burden in caregivers of individuals with dementia
- Caring for Aged Dementia Care Resident Study (CADRES) of person-centred care, dementia-care mapping, and usual care in dementia: a cluster-randomised trial
- Dementia care in a rapidly aging society
- Use of restraints on dementia patients: an ethical dilemma of a nursing staff in Israel
- Relationship between caregiver characteristics and the reported quality of life of people with mild and moderate dementia
- Hospital transfers of nursing home residents with advanced dementia
- Advance Care Planning in Nursing Home Patients With Dementia: A Qualitative Interview Study Among Family and Professional Caregivers