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1,013 studies tagged home, 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 prevalence of dementia in Latin America and the Caribbean is growing rapidly, increasing the burden placed on caregivers.
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We found disparities between black and white residents with ADRD both within and across facilities.
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This study highlights the need for nursing homes to employ specialist nurses who have been trained in the appropriate knowledge and skills to deal with the challenges of end-of-life care for people with advanced dementia and pain.
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74/100
This systematic review highlighted the lack of consensus regarding referral criteria for palliative care in patients with dementia and the need to identify timely triggers to standardize referral.
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Use of the transactional model of stress responses yielded important insights about families coping with dementia.
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Nearly 40% of patients with dementia in our study experienced live discharge or a long length of stay.
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Dementia and cancer occur commonly in older adults.
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51/100
The most impacting factors on digital divide in our population are the social support networks and the experience with the technology: the presence of a digital native caregiver.
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Five overarching themes derived from the interviews were as follows: (a) My life still has value and meaning, (b) I am my own unique individual, (c) I place my trust in other people, (d) The future worries me, and (e) I accept and embrace what life brings.
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The outbreaks added significant additional stress to the nursing workforce, which has historically experienced high turnover, chronic staffing shortages, and increased burnout in long‐term care settings.
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Our findings provide a current overview of published PC-interventions in dementia, which followed heterogeneous approaches under the PCC-concept.
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Psychoeducational program is effective in reducing the family caregivers' perceived burden.
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Looking at the complex effects of a global pandemic through the experiences of people living with dementia and their care partners is vital to inform healthcare priorities to restore their quality of life and health and better prepare for the future.
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This study reports findings from a series of focus groups with persons with dementia and family caregivers intended to explore: (1) perceptions of and experiences with advance care planning (ACP); (2) concerns related to future care including, but not limited to, end-of-life care; and (3) practices that may support positive engagement with ACP.
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Decision-making interventions typically consist of multiple components which aim to establish preferences for future health care.
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Even among patients with early cognitive impairment seen in specialty clinics and their caregivers, most were unaware of the decisions they could face, and there were many barriers to planning for these decisions.
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Importance and objective Conducting advance care planning (ACP) conversations with people with dementia and their relatives contributes to providing care according to their preferences.
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Interventions had, on average, a significant, small-to-moderate effect on the improvement of ability/knowledge, subjective well-being, burden, depression, and the caregiver's anxiety as well as symptoms of the care recipient.
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46/100
COVID-19 pandemic and the lockdown produced psychological consequences in caregivers of pwD, with an increase of levels of depression.
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Persons with dementia are at high risk for loss of decision-making ability due to increased cognitive decline as the disease progresses.
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Eighty-one studies with 3347 participants were included in this review.
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At ward level, professionals and residents rated the average achieved level of shared decision-making 71.53/100 (σ = 16.09) and 81.11/100 (σ = 19.18) respectively.
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Benefit-finding is an efficacious intervention for depressive symptoms in Alzheimer caregivers, with strong effects in the medium-term post-intervention and possible moderate effects in the longer-term post-intervention.
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We found no papers that informed the 'cultural aspects of care' domain.
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Future studies are encouraged to adopt personalized internet-based supportive interventions to improve the health of family caregivers and their care recipients.
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The Namaste Care Family program is dominant over usual care and, thus, cost-effective, although statistical uncertainty was considerable.
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COVID-19 pandemic in Argentina has affected the care of older adults with dementia deeply.
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54/100
Total monthly health care costs for individuals with ADRD are statistically greater (P<0.05) than controls beginning in the third month before diagnosis and remain significantly greater through the eighth month following diagnosis.
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Dementia syndrome is common and expected to increase significantly among older people and characterized by the loss of cognitive, psychological and physical functions.
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These findings have implications for clinical practice and suggest that presence of a caregiver may be an important modifying variable on patient outcomes to examine in future research.
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52/100
Comprehensive nurse practitioner dementia care co-management reduced ED visits, shortened hospital length of stay, increased hospice use, and delayed admission to long-term care.
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Dementia decedents were more likely to die at home and other places and less likely to die at institutional settings over the study period.
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There is a growing interest in using technology to provide meaningful activities for people living with dementia.
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Caregivers reported that digital mental health tools have an overall positive role in their health.
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Knowledge of CPR, MV, TF, and self-efficacy to make EOL treatment decisions increased significantly more in the ACT-Plan group at weeks 4 and 20.
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Current evidence on sex and gender differences in caregiving burden, mental and physical health is limited.
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This review highlighted the main challenges associated with optimal ACP initiation with PwD.
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Advance care planning is acceptable for people with dementia and their carers and is associated with improved outcomes.
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This systematic review and meta-analysis compared the effects of 131 randomized controlled trials, published between 2006 and mid-2018, for dementia caregivers with community-dwelling care-recipients.
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Virtual reality use was generally safe and enjoyable in hPLWD.
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Many identified themes were consistent with published barriers to quality EOL care in dementia.
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Phase 1 (realist review; 86 papers) identified that a key intervention component was the activities enabling the development of moments of connection.
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Prognostic discussions between caregivers of PwD and the PwD's physicians may be occurring more often; however, a high percentage of caregivers report a poor understanding about the terminal nature of dementia and the role of PC.
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Three-year survival after dementia diagnosis can be predicted with good accuracy.
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High levels of caregiver burden are present in a large proportion of caregivers of people with dementia and this increases over time for those without services.
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Future research should focus on ways to involve people with dementia in decision-making through supported means.
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The 780 PWDs (56.3% female; mean [SD] age, 78.1 [9.9] years) and 780 caregivers (70.9% female; mean [SD] age, 64.7 [12.0] years) lived in California (n = 452), Nebraska (n = 284), or Iowa (n = 44).
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Nursing home staff benefits from this training in shared decision-making.
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Policies regarding sustained hospice eligibility should account for the variable and protracted end-of-life trajectory of patients with dementia.
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Our educational intervention increased ACP initiation, and the number of nonmedical and medical preferences discussed.
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.
- Effects of the Namaste Care Family programme on quality of life of nursing home residents with advanced dementia and on family caregiving experiences: study protocol of a cluster-randomised controlled trial
- Sleep Quality of Persons with Dementia and Family Caregivers in Korean Americans: Wearable Technology to Study the Dyadic Association
- Insight for impairment in independent living skills in Alzheimer's disease and multi-infarct dementia
- Palliative and aggressive end-of-life care for patients with dementia
- A user-centred website to support advance care planning for people with dementia and their family caregivers: Development and usability study
- The quality of life in late-stage dementia (QUALID) scale
- Feasibility, acceptability, and preliminary efficacy protocol of an intervention for caregivers of hospice patients living with dementia: A pilot randomized control trial
- The Impact of Dementia Caregiving on the Health of the Spousal Caregiver
- Level of Care Preferences Among Nursing Home Residents With Advanced Dementia
- Antipsychotic therapy and short-term serious events in older adults with dementia