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planning
1,013 studies tagged planning, 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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MBSR was more effective at improving overall mental health, reducing stress, and decreasing depression than CCES.
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Residence in an SCU is associated with some, but not all, markers of better quality end-of-life care among nursing home residents with advanced dementia.
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The results were consistent for both nursing homes and data were aggregated.
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Concerning pain assessment, the findings of this review suggest that self-report pain rating scales, in particular the Verbal Rating Scale, the Horizontal Visual Analogue Scale and the Faces Pain Scale can be administered to patients in a more advanced stage of dementia.
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The experience of being a carer of a person with dementia at the end of life is expressed in these 12 accounts.
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The sources of stress for families of nursing home (NH) residents with advanced dementia have not been well described.
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PIM use may be higher in dementia patients and their informal caregivers compared with the general older adult population.
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There are currently almost three times as many care home beds as NHS hospital beds in England, and the number is projected to rise significantly by 2019 (Laing and Buisson, 2009).
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Several areas of end-of-life care provision could be improved.
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Our results show that regarding end-of-life preferences for patients, there is moderate agreement between patients and their spouses, but limited evidence for projection of spouses' preferences on patients (i.e. spouse making a prediction based on own wishes).
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The evidence is not conclusive as to whether some symptoms are more important than others.
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The majority of hospitalizations of NH residents with advanced dementia were due to infections and thus were potentially avoidable, because infections are often treatable in the NH.
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Grief in dementia carers can be expected; however, those at risk of distressing anticipatory and complicated grief may be identified and targeted for intervention when necessary.
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43/100
Qualitative methods of service evaluation facilitated a broader and deeper understanding of a range of perspectives, which, with other components of rapid participatory appraisal, generated potential solutions to improve care.
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Nursing home residents receiving palliative care are more likely to have a GP order.
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A systematic review of the literature was conducted to examine the relationship between ethnic minority status and provision of end-of-life care for people with dementia.
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Future studies should consider culturally tailoring interventions for Hispanic/Latino caregivers from differing subcultures, utilizing relevant technology in studies, and evaluating the functional level of the care receiver and assess where he/she is in the disease process continuum.
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Because previous research favored care in the Netherlands to that in the United States, findings suggest improvement in end-of-life care and outcomes in the United States and stability in the Netherlands.
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Dual hospice/SNF access may result in fewer hospital deaths and higher quality of life for dying NH residents.
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Our aim was to review systematically the effectiveness of ACP interventions in people with cognitive impairment and dementia.
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One in three adults over the age of 60 years will die with dementia.
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Four themes were identified: Making the transition; Competence challenged; 'The long view' and Working together.
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The quality of end-of-life care exists on a continuum across care settings.
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A five-point action plan designed to drive up the quality of hospital care for people with dementia is to be issued by the RCN this week.
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69/100
A decision aid about feeding options in advanced dementia reduced decisional conflict for surrogates and increased their knowledge and communication about feeding options with providers.
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The current evidence base for ACP in dementia is limited.
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The staff require education and support about discussing and implementing plans around care at the end of life in dementia and about cultural issues around death to improve practice.
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Our comparative study of psychometric properties of instruments allows for informed selection of QOC and QOD measures for LTC residents with dementia.
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Bereaved family members of people with dementia who received hospice reported higher perceptions of the quality of care and quality of dying.
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This article is a report on a study of the multidimensional predictors of caregiver burden in caregivers of individuals with dementia using nationally representative data.
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Advance directives for euthanasia are never adhered to in the Netherlands in the case of people with advanced dementia, and their role in advance care planning and end-of-life care of people with advanced dementia is limited.
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Self-efficacy is the belief that one can perform a specific task or behaviour and is a modifiable attribute which has been shown to influence health behaviours.
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The booklet is suitable to inform Dutch and Canadian families on comfort care in dementia, but implementation in Italy requires further consideration.
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Design qualitative exploration of views from care home staff and the family of residents in care homes for older people.
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Support groups benefit caregivers and findings of this meta-analysis serve as immediate guidance for group facilitators.
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Rural subjects with higher health literacy were more likely to want comfort care compared to those with lower levels of health literacy.
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Patients with advanced dementia often receive poor end-of-life care.
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Medicare expenditures among nursing home residents with advanced dementia vary substantially.
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Over 40% of US NH decedents have mild-to-moderately severe or advanced dementia.
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A minority of NH residents with advanced dementia received hospice care.
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51/100
Despite the growing body of evidence over the 20 years of this review, and the widespread interest in family dementia caregiving generally, much of the research exploring family caregiving in rural areas focuses on the experience, use and barriers to formal service provision.
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The ADRQL is a valid indicator of QOL in NH residents with advanced dementia.
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Whether there is a difference in impact between EOD and LOD on caregivers is still unclear.
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Ninety-four percent of hospices and 72% of PC programs had served at least one patient with a primary diagnosis of dementia within the past year.
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When prospectively validated at the bedside and used as a continuous measure, the ability of the ADEPT score to identify nursing home residents with advanced dementia at high risk of death within 6 months was modest, albeit better than hospice eligibility guidelines.
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A mortality risk score derived from MDS data predicted six-month survival in advanced dementia with moderate accuracy.
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Memory clinics have been promoted as opportunities for improving dementia diagnosis and care.
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Using a knowledge-translation framework, information and strategies can be provided to family and professional caregivers to help them optimize residual memory and communication in people with dementia.
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Among community-living dyads, a nonpharmacologic biobehavioral environmental intervention compared with control resulted in better outcomes for COPE dyads at 4 months.
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Each vignette promoted discussion of differences of perspectives about the ways to enhance the dignity of people with dementia in hospital, care home and community settings.
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.
- Understanding Digital Literacy of Persons With Dementia and Their Caregivers: A Scoping Review and an Evolutionary Concept Analysis of Empirical Studies
- Medical decision-making experiences of persons with dementia and their carepartners: a qualitative study
- Convening Hispanic/Latino Caregiving Advisors for Inclusive Research in Dementia Palliative Care
- Use of Digital Health Technologies for Dementia Care: Bibliometric Analysis and Report
- Advance care planning for people with dementia
- Exploring advance care planning discourses in scottish dementia policies: A critical discourse analysis
- How to create value with unobtrusive monitoring technology in home-based dementia care: a multimethod study among key stakeholders
- The advance care planning experiences of people with dementia, family caregivers and professionals: a synthesis of the qualitative literature
- End of life care interventions for people with dementia in care homes: addressing uncertainty within a framework for service delivery and evaluation