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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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Dementia, particularly Alzheimer's Disease, continues to be a significant global health concern, driven by increasing prevalence as the population ages.
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Among the 13 604 086 traditional Medicare beneficiaries included in the study (mean [SD] age, 79.4 [7.7] years; 60.4% women), 27.7% had a diagnosis of dementia.
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Participants sought to feel secure by following recommended practices, manage uncertainty, avoid crises, share burdens within families, and avoid poor end-of-life experiences.
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45/100
NPs reported that the quality of dementia care in their practices is poorer than the overall care provided.
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Assistive technologies hold significant potential to enhance the quality of life for persons with dementia and their caregivers by addressing key concerns related to safety, independence, and social inclusion.
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In known-group validity analysis, the EQ-HWB instruments performed similarly to the C-DEMQOL in terms of effect sizes across a range of variables and slightly better than the CarerQol on some variables.
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This review included six articles, and nine categories emerged from the findings.
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There were few differences in how MA plan characteristics affected choice among older adults with and without dementia.
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Of 162 034 eligible Medicare beneficiaries (mean [SD] age, 85.0 [7.9] years; 94 304 female [58.2%]), 51 191 (31.6%) were attributed to MSSP ACO.
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The implementation of a transmural model of early palliative care for patients with advanced dementia requires the coordination between clinicians in the tertiary care setting and community, together with health information technologists.
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The ResQ-Care-Dem scales' internal consistencies ranged between 0.65 and 0.81.
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Within-day analyses revealed time with CRs was associated with increased HR, primarily due to negative interactions.
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Estimates suggest a high social burden from ADRD, with annual costs increasing from 0.9% to 3.8% of gross domestic product between 2019 and 2050.
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Eighty respondents (8.1%) care for 90 individuals with neurocognitive disorders, a majority of whom are parents of the respondent.
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Participants found MATCH acceptable (combined AES median score of 28, range 25-34) and useful (SUS median score of 73.5, range 55-100).
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In this Delphi survey study, international experts reached consensus on a range of criteria for referral to specialist palliative care.
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BackgroundLet's Talk Tech (LTT) is a self-administered web intervention for people with memory loss and their care partners that supports decision-making about digital health technologies.
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People living with dementia and their care partners benefit from services and supports from a wide variety of healthcare and social service professionals.
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Out of 163 caregivers invited to participate, 104 (64%) participated.
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Future research should leverage perspectives of former caregivers to assist with improving outcomes for Black caregivers, thereby promoting health equity. [ Journal of Gerontological Nursing, 51 (6), 30–37.]
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30/100
As the population of older adults continues to grow, the prevalence of dementia is increasing dramatically.
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The first three elements concerned common awareness of collaborative ACP in dementia care, role clarification for various professions and actively working towards shared goals in collaborative ACP in dementia care.
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This study presents findings from IDEA Café, for older adults aged 50 and older living with early dementia, dementia, Alzheimer’s Disease or cognitive impairment (ED/CI) with no informal caregiver or care partner.
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In the dementia scenario, 26.9% of participants preferred unlimited medical treatment.
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Current Care and Support: Four themes emerged: Communication with empathy; Written information valuable but could be overwhelming; Referrals provided but not necessarily followed; A focus on prescribed anti-dementia medications.
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In this study, the total scores of caregiver burden, family resilience, and SOC were 45.64 ± 17.04, 175.30 ± 34.38, and 52.29 ± 15.91 among family caregivers of people with dementia.
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These inputs and activities were shown in the logic model to result in short, medium, and long-term outcomes, including reduced healthcare resource use and increased quality of life for people with dementia at the end of life.
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We interviewed 30 participants (9 PWD, 21 carepartners).
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A balanced understanding of dementia’s impact (acknowledging both continuity and loss, alternatives and socially constructed aspects) better reflects the realities of dementia and creates new possibilities for supportive care practices to improve pain management and quality of life.
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52.7% of dementia caregivers in the United States experience financial toxicity.
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Four main themes and 10 subthemes were identified.
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One factor accounted for 79.0% of the variance in the UCLALS3; it was perfectly invariant across genders but variant at the metric level across countries.
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Unmet PC needs were highly prevalent (78.2%).
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Thirty-four reviews were included, published between 2009 and 2023.
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Three main categories were created: (1) Impact of observed cognitive decline, (2) Impact of diagnosis on service engagement, and (3) Support and follow-up for family caregivers.
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The review consistently identified high levels of perceived stress among dementia caregivers.
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For 2018 and 2019, 3.5% and 5.4% received ACP visits, and 0.4% and 0.5% received CAACPS visits, similar to use reported elsewhere.
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Remote monitoring (RM) technology can support home-based dementia care by enabling (in)formal caregivers to monitor the health and safety of people with dementia remotely.
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The ACT group reported significantly greater improvements in stress (P=.043) and psychological QoL (P=.014) in the posttest compared to the control group.
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Dagmarsminde's holistic care philosophy integrates rehabilitation, palliative care, and "Omsorg" to empower residents in expressing their identity and engaging in a meaningful community.
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Dementia is a syndrome characterised by the development of multiple cognitive deficits and behavioural changes that significantly interfere with various aspects of life.
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We enrolled 32 patients, 32 caregivers, and 25 clinicians.
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48/100
People with dementia were on average 80.6 years old, mostly female (56%) and mildly to moderately cognitively impaired (85%). 98.6% of the participants had at least one need, of which just over a third (36.5%) were rated as met and just under two-thirds (63.5%) as unmet.
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With the rising number of dementia cases, supporting family caregivers to maintain their well-being is crucial.
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Sixty studies were identified. Mental and physical effects caused by caregivers' sleep deprivation have been observed.
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= 0.01). We also found that greater use of emotion-focused coping and deriving greater gains in caregiving mitigated the negative association between caregiver financial difficulty and their distress and perception of PwSDs' well-being.
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For co-residing care partners, high (p = 0.001), increased (p = 0.001), and decreased (p = 0.001) fall frequency over 2 years was significantly associated with emotional difficulties.
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Probable dementia caregiving predicted worse sleep quality, which mediated the relationship with higher depressive symptoms.
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BackgroundThere are 5.5 million people living with dementia in the United States (US), with the cost of unpaid care making up a significant portion of the care costs.
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(n = 14) included NH administrators and other leaders, palliative care providers, telehealth representatives, dementia advocates, a care partner, and a PLWD.
From across this tag
9 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 9. The same 9 appear here every time.
- Comfort goal of care and end-of-life outcomes in dementia: A prospective study
- Concordance between Goals of Care and Treatment Decisions for Persons with Dementia
- Better palliative care for people with a dementia: summary of interdisciplinary workshop highlighting current gaps and recommendations for future research
- Advance care planning in dementia: recommendations for healthcare professionals
- Institutional Special Needs Plans and End-of-Life Outcomes for Nursing Home Residents With Dementia
- Unraveling the subjective well-being of formal and informal caregivers for people with dementia: a comparative analysis
- The Evaluation of Telehealth’s Impact on Medicare Annual Wellness Visits and Dementia Diagnosis
- Advance Care Planning for African American Caregivers of Relatives With Dementias: Cluster Randomized Controlled Trial
- An audit of palliative care in dementia