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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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Of these, a growing number have secured funding, initiated collaborations, contributed to dementia palliative care research, and increased confidence and comfort with conducting clinical trials (p<.05).
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There were no significant differences in self-efficacy related to obtaining respite and RDPB between SES groups.
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40/100
We found a significant increase in the likelihood of AWV uptake among telehealth adopters by 10.2 percentage points (p <0.001) than non-adopters of telehealth in traditional FFS Medicare plans.
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40/100
We found a significant increase in the likelihood of AWV uptake among telehealth adopters by 10.2 percentage points (p <0.001) than non-adopters of telehealth in traditional FFS Medicare plans.
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30/100
Our study underscores the role of telehealth in increasing AWV uptake and facilitating cognitive assessments.
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37/100
Hospice use (2011-2021) for decedents with cancer and dementia by ethnic and racial groups.
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Although ACP programs in nursing homes may increase DNR directives, evidence of other EoL outcomes remains limited and inconsistent.
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The proposed model demonstrated a sound fit (PCMIN/DF = 2.612).
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• AT use was limited and AT type used varied by caregiver living arrangement. • Most used ATs: daily living support and risk prevention; risk response least used. • Daily living support ATs linked to fewer care hours. • Risk prevention ATs tied to longer PT, higher CarerQol-7D, and lower SRB scores. • Daily support and risk response ATs most likely to extend PT by over six months.
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The 29-item needs assessment showed strong internal consistency, with a mean Cronbach’s alpha of .89 and McDonald’s omega of .90.
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Dementia-specific ACP/AD require a relational, flexible and ethically grounded approach that evolves with the individual’s condition.
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Among 259 945 decedents with dementia (mean [SD] age, 85.8 [8.0] years; 60.4% female), 8.3% were non-Hispanic Black, 4.4% were Hispanic, and 87.3% were non-Hispanic White.
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A total of 414 caregivers participated. They exhibited normal intensity of depression, anxiety, and stress symptomatology.
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Frequently reported factors included self-management support, information access, and enhanced communication, although these were not consistently addressed across all reviews.
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Informal caregivers often seek additional support.
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Forty studies were included. Key stakeholders included healthcare professionals (HCPs); family members and caregivers; PWD; dyads (PWD and their caregivers); the broader public; policymakers; and researchers.
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Forty studies were included. Key stakeholders included healthcare professionals (HCPs); family members and caregivers; PWD; dyads (PWD and their caregivers); the broader public; policymakers; and researchers.
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57/100
Ninety-one reviews provided evidence on the impact of telemedicine in dementia care.
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Dementia significantly impacts cognitive, behavioral, and functional abilities, creating challenges for both individuals and caregivers.
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Nearly half (48%) of older adults experienced an inpatient admission, and nearly all (92%) experienced a potentially burdensome intervention.
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We have enrolled 29 clinicians and 53 FCPs and aim to have 24 clinicians matched with 96 FCPs (N = 120) to complete the intervention.
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38/100
In phase 1, the mean system usability scores increased from 65.4 (SD 11.8) in round 1 to 73.8 (SD 15.9) in round 3, exceeding the benchmark of 68.
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Advance care planning aims to allow individuals to discuss their goals and preferences for future medical and nursing care with family members and medical personnel in advance when they still have decision-making ability, so that individuals can receive medical care that meets their preferences when they lose their decision-making ability.
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36/100
Of 343 palliative care evaluations (for 322 unique patients), 38% were of patients who identified as African American/Black, 38% as White, 9% as Asian/Pacific Islander, and 15% as other races; 41% were of patients who identified as Hispanic/Latino (measured separately from race); 80% were of female patients; and the mean patient age was 88 years.
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Written by leaders of six established comprehensive dementia-care programs (including Care Ecosystem, MIND at Home, and BRI Care Consultation) that helped shape the CMS GUIDE model, this paper lays out a practical four-step roadmap for organizations trying to launch or sustain comprehensive dementia care programs like GUIDE.
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42/100
Using LGBTQ+ Social Networks, Aging, and Policy Study Wave 3 data (N = 982), this study examines how caregiving for individuals with mild cognitive impairment, Alzheimer’s disease, and related dementias (MCI/ADRD) impacts everyday stressors, discrimination, and health outcomes among LGBTQ+ older adults in the Southern United States.
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Three themes identified include (a) LOVOT's role in supporting engagement and stimulating conversation, (b) the irreplaceability of human touch and emotional nuances, and (c) concerns about ownership and equitable resource allocation.
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Of 9872 individuals, 3563 (36%) died within 6 months.
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This study examined how nursing home staff adapt to challenging mealtime behaviors in residents with dementia, such as turning away or refusing food.
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Four themes emerged: layered caregiving burden, cultural strain and emotional dissonance, dual emotional experiences of caregiving, and coping strategies and unmet needs.
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Four GPs and eleven physicians were interviewed, and four major themes emerged: (1) knowledge of best practices of BPSD management, (2) awareness of current challenges in BPSD management, (3) non-involvement, blame shifting and rationalisation: perceived reasons for the current challenges and (4) suggested solutions.
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43/100
= 18 556) lived in care homes before death.
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The final models included six predictors: caregivers' social support, caregivers' employment situation, caregivers' average daily care duration, caregivers' monthly family income, caregivers' self-efficacy and PwD's chronic disease.
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Overall, 75.9% of the caregivers reported experiencing at least a mild burden, and the levels of depression, anxiety, and stress among the caregivers were higher than expected.
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Latino family caregivers of people with dementia face significant challenges and limited access to support.
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Alzheimer's Disease and Related Dementias (AD/ADRD) are progressive neurodegenerative conditions that impair memory, thought processes, and functioning.
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Person-centered care provides a critical framework for dementia support in long-term care facilities, emphasizing attention to each resident's evolving needs, personal history, preferences, and values.
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BackgroundClinician communication at the time of a dementia diagnosis often inadequately addresses patient and caregiver needs.
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Improving digital technology for caregivers requires studies with larger populations and longitudinal outcomes.
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Nineteen articles involving 142,772 participants were included.
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We previously demonstrated that PST/DSJ improved caregiver burden and depressive symptoms among caregivers of adults with Alzheimer’s Disease and related dementias (ADRD), regardless of the number of sessions or boosters received.
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Beyond these practical challenges, caregivers often endure significant physical exhaustion and sleep deprivation from the unrelenting demands of caregiving, which can lead to chronic fatigue and deteriorating health (Liu et al., 2022; Mao et al., 2024).
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Individuals living alone with dementia are rising rapidly, yet this group remains largely unrecognized in dementia care planning.
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We identified two main themes (each with subthemes) that influence Latino dementia caregiver experiences with healthcare: (1) caregiving and understanding of dementia shaped by individual, family, and social factors (subthemes: Caregiver's own understanding of dementia; Lack of support and understanding from family; Latino cultural perspectives on dementia); and (2) navigating formal services amid gaps in cultural alignment and support (subthemes: Trial and error: education and resource gaps; Cultural tension with healthcare).
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Three themes were identified: (1) Struggling with conflicting emotions and social challenges - caregivers reported experiencing stress, physical exhaustion, and emotional strain due to constant availability and the challenges of managing behavioral changes, further intensified by isolation and shrinking social networks.
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60/100
In this national case-control study of nursing home residents with ADRD receiving hospice care, initiation of benzodiazepine or antipsychotic use was associated with increased 180-day mortality.
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38/100
Most dementia caregiver programs focus on a single caregiver, overlooking diverse caregiving networks that include family, friends, and relatives who provide care.
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The results provide evidence for the efficacy and cost-effectiveness of extended nursing roles in dementia care, demonstrating that extended nursing roles reduce unmet needs and improve quality of life.
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A total of 172 participants were randomized.
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All dyads had at least one unmet need. A combined model incorporating predictors from both PWD and caregivers indicated that PLWD having lower education, being male, and exhibiting more neuropsychiatric symptoms are associated with more unmet needs.
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.
- Community based occupational therapy for patients with dementia and their care givers: randomised controlled trial
- End-of-life care and the effects of bereavement on family caregivers of persons with dementia
- Taking Care of the Dyad: Frequency of Caregiver Assessment Among Veterans with Dementia
- Storytelling in family-provided care - developing diversity-sensitive stories for family caregivers of Turkish individuals living with dementia
- Effect of Mindfulness-Based Stress Reduction Activities on Family Caregiver Burden in Patients With Dementia—A Pilot Study
- Palliative care for people with dementia in the terminal phase: a mixed-methods qualitative study to inform service development
- The Determinants of Quality of Life of Nursing Home Residents with Young-Onset Dementia and the Differences between Dementia Subtypes
- Advocacy and Palliative Care as a Framework for Dignified Dementia Care in African Settings
- The Use of Telehealth Among People Living With Dementia-Caregiver Dyads During the COVID-19 Pandemic: Scoping Review
- Advance care planning in nursing homes: correlates of capacity and possession of advance directives