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nursing
1,013 studies tagged nursing, 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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Tailoring activities to the capabilities of dementia patients and training families in activity use resulted in clinically relevant benefits for patients and caregivers.
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To evaluate the impact hospice enrollment has on the terminal care of patients with dementia and describe the symptom burden these patients experience, caregivers of dementia decedents were assessed in a mortality follow-back survey.
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60/100
Psychosocial intervention makes a vital contribution to dementia care.
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Counseling and support preserved SRH in vulnerable caregivers.
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The original mortality risk score predicted 6-month mortality with reasonable accuracy in 2 validation cohorts of nursing home residents with advanced dementia.
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Of 359,474 cognitively impaired residents, 49% had a diagnosis of dementia.
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The 10/66 DRG baseline population-based studies are nearly complete.
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Dementia is a progressive life limiting condition with increasing prevalence and complex needs.
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Dementia is a leading cause of death in the USA.
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42/100
This paper examined the emotional impact of diagnosis disclosure on recently diagnosed people with dementia.
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The results showed that 68.02% of caregivers were highly burdened and 65% exhibited depressive symptoms.
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We conducted a systematic review of the use of quality of life (QoL) measures as outcome in pharmacological and nonpharmacologic intervention trials in patients with Mild Cognitive Impairment or dementia, and their proxies.
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43/100
Patients who survive to the final phase of dementia are more likely to die from cachexia or dehydration than those who die before.
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Watching the video significantly changed preferences for care, transcending apparent differences in preferences associated with race/ethnicity and educational level.
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This article reviews the Dutch societal debate on euthanasia/assisted suicide in dementia cases, specifically Alzheimer's disease.
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Effects of caregiving on physical health have received less theoretical and empirical attention than effects on psychological health.
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The burden associated with BPSD is different for each symptom and does not always depend on frequency and severity of BPSD.
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Estimates suggest that there are more than 10 million adult caregivers of persons with dementia, two-thirds of who experience some form of sleep disturbance during the course of their caregiving career.
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Advance care planning ideally includes communication about values between patients, family members, and care providers.
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38/100
Providing palliative care for residents with dementia in long-term care (LTC) settings is problematic due to their declining verbal abilities and related challenges.
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46/100
DEMQOL and DEMQOL-Proxy show psychometric properties that are comparable with the best available dementia-specific measures of HRQL.
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We found excellent evidence for the efficacy of six or more sessions of individual behavioral management therapy centered on the care recipient's behavior in alleviating caregiver symptoms both immediately and for up to 32 months.
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This landmark NIH-funded trial (REACH II) tested a structured, multi-part support program for 642 Hispanic, White, and Black family caregivers of people with Alzheimer's or related dementias across 5 U.S. cities.
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Occupational therapy improved patients' daily functioning and reduced the burden on the care giver, despite the patients' limited learning ability.
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73/100
This randomized trial of 406 spouse caregivers of people with Alzheimer's tested whether counseling and support (six counseling sessions, mandatory support groups, and on-call phone counseling) could delay nursing home placement.
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Caring for elderly people with dementia is associated with well-documented increases in burden, distress, and decrements in mental health and wellbeing.
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A structured multicomponent intervention adapted to individual risk profiles can increase the quality of life of ethnically diverse dementia caregivers.
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73/100
Greater access to effective programs of counseling and support could yield considerable benefits for caregivers, patients with Alzheimer disease, and society.
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A dementia guideline-based disease management program led to substantial improvements in quality of care for patients with dementia.
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Better communication, greater resident comfort, no tube feeding, and care in a specialized dementia unit are modifiable factors that may improve satisfaction with care in advanced dementia.
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Coping style may be more associated with anxiety than depression while other covariates (burden and poor physical health) are similar to those for caregiver depression.
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Frontotemporal dementia (FTD) is the second most prevalent dementia after Alzheimer's disease (AD).
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We included 134 consecutive bedridden end-stage dementia patients admitted during a 36-month period, and surviving in the ward for <6 months.
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48/100
This study identifies predictors of complicated grief for which interventions could be developed to not only ease caregiver distress, but also serve as preventive interventions for bereavement.
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Rural residence was also associated with lower risk of more than 10 days of hospitalization and ICU admission.
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The life expectancy of patients who have dementia and are initiated on dialysis in the United States has not been described in the medical literature.
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Despite the growing number of persons with advanced dementia, and the need to improve their end-of-life care, few studies have addressed this important topic.
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38/100
The lack of valid and reliable instruments designed to measure the experiences of older persons with advanced dementia and those of their health care proxies has limited palliative care research for this condition.
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Despite providing high-intensity care, often for years, many bereaved caregivers perceived themselves as unprepared for the death.
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Because most interventions have domain-specific outcomes, clinicians must tailor interventions according to the specific needs of the individual caregivers.
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Caregivers of FTD patients were overall more distressed by the behaviour of their partners than were the caregivers of AD patients.
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Collaborative care for the treatment of Alzheimer disease resulted in significant improvement in the quality of care and in behavioral and psychological symptoms of dementia among primary care patients and their caregivers.
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No correlation with neuropsychiatric symptoms such as apathy and depression was found.
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Caregivers' reasons for placement included (a) the need for more skilled care (65%); (b) the caregivers' health (49%); (c) the patients' dementia-related behaviors (46%); and (d) the need for more assistance (23%).
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Pneumonia is a common terminal event in advanced dementia for which many patients receive parenteral antibiotics.
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These data suggest that quality of life in dementia is complex, and that simple proxy substitutions of discrete measures such as cognition or function are likely to miss important factors.
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Most rural focus group participants voiced unqualified acceptance of death and placed few conditions on death, beyond their hope that it would be quick and peaceful.
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Unmet need may be useful in identifying dementia care recipients at risk for nursing home placement and death.
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Those who viewed Caregiver's Friend: Dealing with Dementia 30 days postexposure demonstrated significant improvements in depression, anxiety, level and frequency of stress, caregiver strain, self-efficacy, and intention to seek help, as well as perceptions of positive aspects of caregiving.
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Only behavior management therapies, specific types of caregiver and residential care staff education, and possibly cognitive stimulation appear to have lasting effectiveness for the management of dementia-associated neuropsychiatric symptoms.
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.
- Nursing home residents dying with dementia in Flanders, Belgium: a nationwide postmortem study on clinical characteristics and quality of dying
- Primary care and dementia: 2. Long-term care at home: psychosocial interventions, information provision, carer support and case management
- Interventions to reduce the burden of caregiving for an adult with dementia: a meta-analysis
- The Self-Care Needs and Behaviors of Dementia Informal Caregivers: A Systematic Review
- The Evaluation of Telehealth’s Impact on Medicare Annual Wellness Visits and Dementia Diagnosis
- Impact of assistive technologies on caregiver burden and perseverance for people with dementia at home
- Refining a Digital Therapeutic Platform for Home Care Agencies in Dementia Care to Elicit Stakeholder Feedback: Focus Group Study With Stakeholders
- Caregiver burden in end-of-life care: advanced cancer and final stage of dementia
- Understanding Challenges and Emotions of Informal Caregivers of General Older Adults and People With Alzheimer Disease and Related Dementia: Comparative Study