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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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One hundred sixteen participants consented and 93 (46 waitlist control, 47 intervention) were included in the analyses.
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Critical appraisal will not be undertaken, as it is optional in scoping reviews and is not aligned with the primary mapping objectives of this review.
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Despite comprising the largest segment of the sexual minority population and experiencing unique stressors and health disparities, bi+ dementia caregivers remain underrepresented in health and caregiving research.
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44/100
At baseline, nearly one-third of caregivers reported moderate-to-severe burden (mean ZBI 31.4 ± 15.4), a prevalence that persisted at 6 months.
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The CES effectively distinguished between different levels of caregiver strain.
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A significant association between increased caregiver burden and BPSD in patients with AD was demonstrated, which may be associated with decreased caregiver healthcare and social care-related QOL.
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LPA supported a three-profile solution: (1) lower depressive symptoms with moderate anxiety (33%), (2) severe combined depression and anxiety (18%) and (3) moderately severe depression with severe anxiety (49%).
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The caregivers in intervention group showed significant reductions in distress scores for dressing, personal hygiene, communication, and behavioural and psychological care problems at both the 6th and 12th week assessments.
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36/100
China has the world's highest dementia prevalence, disproportionately impacting rural areas.
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Broad barriers identified in the outer setting of the implementation framework include sociocultural values and a lack of supportive policies, guidelines, and financing.
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Palliative care was associated with a higher risk of hospitalization in the first 90 days (e.g., hazard ratio (HR) 1.43 at 30 days; 95% confidence interval (CI) 1.25-1.64), which was driven predominantly by hospitalization with palliative intent, but was no longer significantly different beyond 180 days, compared to not receiving palliative care. [Correction added on 31 January 2026, after first online publication: The preceding sentence has been revised in this version.]
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After screening, a total of 48 studies were included in this review.
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The effects on depression and other outcomes were consistent with those observed for in-person programs, suggesting the viability of well-designed automated intervention.
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Future studies should prioritize short-term interventions and develop integrated approaches combining individual and group formats.
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Seventy-six percent (23/30) of enrolled dyads successfully completed the study.
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Three changes to the intervention content were determined from the different sources of data.
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Thirty articles met the inclusion criteria.
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A total of 53 stakeholders participated in focus groups and engagement sessions.
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Among 209,468 decedents, 95,594 were selected after matching.
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Three cohorts of interdisciplinary scholars (N = 53) have started and two have completed DEM-PCCT.
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25/100
This study examined how the COVID-19 pandemic altered the sociologic, individual, and biologic personhood of residents living with dementia in nursing homes, guided by Buron’s (2008) Personhood Model for Dementia Care (PMDC).
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Seven studies were included from 1,800 screened.
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As of October 2025, we have recruited 200 participants.
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31/100
Caregivers considered telemedicine useful, accessible, and safe, facilitating the continuity of care and strengthening the caregiver–professional relationship.
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Music Interventions for Dementia and Depression in Elderly care was a large, multinational, cluster-randomised controlled trial with a 2 × 2 factorial design to examine the effects of group music therapy, recreational choir singing, or both compared with standard care.
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BackgroundEvidence on the effects of caregiver-assisted combined exercise and cognitive interventions for persons with dementia (PwD) is inconsistent.
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There were 361 deaths. Median survival was longer for residents with advanced dementia and frailty (16.5 months, 95%CI:13.5–19.5 months, P < 0.001) compared to incurable cancer (8.1 months, 95%CI:5.1–11.1 months, P < 0.001) and end-stage organ failure (7.7 months, 95%CI:3.0-12.4 months, P < 0.001).
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Carers' knowledge about dementia was moderate overall, with higher scores among those with greater education and previous dementia exposure.
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Palliative care offers specialized care /support to persons with advanced disease, including Older Persons living with dementia related problems.
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Advance care planning (ACP) in dementia has been defined as a communication process adapted to the person’s capacity, which includes, and is continued with family, in our European Association for Palliative Care Delphi study Delphi study with an expert panel from 33 countries.
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Artificial intelligence (AI) has gained attention as a tool to support dementia care through efficient and personalized interventions.
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A greater number of needs (B=.42), polypharmacy (B=.33), and unmanaged symptoms (B=.31) significantly predicted higher triage priority (p<.001).
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27/100
Puerto Rico is experiencing a rapidly aging population due to outmigration and other demographic changes.
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With increasing dementia prevalence and reliance on spousal care partners, understanding how caregiving identity evolves and how resilience is fostered across the care trajectory is crucial.
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Of 1,073 caregivers, 33% reported high baseline strain.
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44/100
Various approaches to advance care planning are in use and generally acceptable also for persons with dementia and their care partners.
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Riverside Health has developed a new palliative care pathway to serve as an innovative standard of person-centered care for persons living with dementia (PLWD) and their care partners.
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1 in 3 older adults die with or from dementia.
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37/100
Most persons with dementia in the U.S. die in long-term care communities.
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Although there were differences between and within the countries, end-of-life care was often affected by the socioeconomic contexts, which represent barriers for access to healthcare services; under-tapped informal caregivers' potential; societal norms and cultural expectations around care and informal caregiving; the dementia-trajectory itself; and an inadequate assurance of policies, skilled workforce, and services.
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30/100
As dementia progresses to advanced stages, the need for compassionate and person-centred care becomes paramount.
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Medicare-funded home health care (HH) is a crucial resource helping Persons with Dementia (PwD) meet their care needs while aging in place.
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These findings suggest that moving to an AL influences Medicare enrollment decisions; and, variation in switching exists between the type of AL (general vs memory care) and whether or not an individual has dementia.
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These findings suggest that moving to an AL influences Medicare enrollment decisions; and, variation in switching exists between the type of AL (general vs memory care) and whether or not an individual has dementia.
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We found significant county-level variability in utilization of high-quality home health.
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Patients and their caregivers and families confronting dementia often face heavy burdens from difficult-to-control symptoms, uncertainty about the future, and a high risk of care partner burnout.
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Antecedents of acute care use and poor prognosis may suggest late utilization of palliative care among PLWD and lack of palliative care needs screening.
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Palliative care should be introduced as a culturally tailored set of services to assist families in ways that align with their values and caregiving practices.
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A total of 88 validated scales were identified.
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Caregiver burden is a multidimensional phenomenon with significant effects on health and well-being.
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.
- Palliative care for end-stage dementia: a discussion of the implications for education of health care professionals
- Use of the QOL-AD for measuring quality of life in people with severe dementia--the LASER-AD study
- Palliative Care for Patients with Dementia: A National Survey
- The role of spirituality among nursing home staff caring for residents with advanced dementia: a qualitative descriptive study
- The Effect of a Comprehensive Dementia Care Management Program on End-of-Life Care
- Respite time-use among dementia caregivers
- Caregivers’ burden analytics: combining variables from patients with dementia and their caregivers
- Barriers and facilitators to implementing person-centred dementia care in long-term care facilities in Western and Asian countries: a scoping review
- An ethnographic study of strategies to support discussions with family members on end-of-life care for people with advanced dementia in nursing homes
- Barriers and facilitators to home-based end-of-life care for people with dementia: A meta-ethnographic study