Home › Research › Topics › planning
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.
-
I consider applications of “AI extenders” to dementia care.
-
The evolving composition and experiences of the family caregiver workforce have profound ramifications for public policy but are not well understood.
-
Family caregivers provide essential care and support for individuals living with dementia, yet their contributions and needs are often unrecognized within formal health care systems.
-
On average, surveyed caregivers (n = 431) were 78.3 years, had 16 years of education, and were mainly White (88.5%).
-
37/100
Key reflections from advisor meetings guided cultural adaptation: lived experiences on dementia caregiving; patient, caregiver, and clinician interactions in the health care system; and limited knowledge and misconceptions of palliative care.
-
Up to 60% of people living with dementia who reside in care homes will ‘wander’ at some point.
-
Dementia’s escalating incidence, coupled with its economic burden, highlights the need for architectural designs and forms that benefit people living with dementia.
-
This study examined relationships among caregiver burden, depressive symptoms, and key processes related to psychological flexibility (experiential avoidance, cognitive fusion, values-driven actions, and mindfulness) in 157 family caregivers of individuals with dementia in the United States.
-
49/100
Due to the ageing population throughout the world, the rates of older adults suffering from dementia are increasing, requiring a closer look at this population.
-
39/100
We showed that consumer wearables are a valid tool for long-term data collection in this vulnerable patient population.
-
Thirty-three studies were included. Over half were conducted in Western countries (n =20).
-
A total of 30 articles were included. These detail the multifaceted responsibilities of clinical pharmacists in primary care for older people.
-
This paper presents the results of a long-term exploratory study that examined the social and emotional impact of using a social robot with a variety of applications to promote activities for people with advanced dementia and their caregivers.
-
The family caregivers of PwD exhibited a fair QoL, with a score of 29.01 ± 4.059.
-
All concurrent validity correlations followed the expected directionality, with 19/21 inter-scale correlations in the total sample reaching statistical significance (p<0.05), and 17/21 reaching at least a low correlation (0.3).
-
Twenty-five studies met the inclusion criteria.
-
The Shifting Expectations narrative indicated that PwD's needs shifted to co-constructed needs with their family as PwD's independence declined.
-
The average life expectancy of people with dementia at time of diagnosis ranged from 5.7 years at age 65 to 2.2 at age 85 in men and from 8.0 to 4.5, respectively, in women.
-
In total, 3028 posts were retrieved, including 1552 from older adult-related subreddits and 1476 from Alzheimer disease-related subreddits; 18 key topics were identified, with the most frequent topics being expressing feelings (2178/3028, 71.93%) and seeking advice and support (1982/3028, 65.46%).
-
Implementation efforts resulted in the adoption of the Care Ecosystem at 28 health systems and eight community-based organizations, including 22 participants in Medicare's Guiding an Improved Dementia Experience (GUIDE) payment model.
-
Eighteen of 24 participants completed the survey and 15 participated in interviews.
-
The analysis revealed five distinct themes: (1) impact of the program, (2) facilitators enhancing participation, (3) barriers hindering participation, (4) suggestions for improving participation and (5) challenges to adopt digital platforms.
-
Website goals were: providing ACP information and facilitating ACP conversations.
-
Recommendations vary by medication type and symptom severity.
-
The rising prevalence of Alzheimer's disease and Alzheimer's disease–related dementias has led to renewed public discourse and policy changes in response to the care needs of persons living with dementia and their care partners.
-
26/100
Otępienie to zespół objawów wywołany postępującymi chorobami neurodegeneracyjnymi mózgu, które prowadzą do znacznego pogorszenia funkcji poznawczych, a w końcowym etapie do całkowitej zależności pacjenta od otoczenia.
-
The observation group had significantly lower Self-Rating Anxiety Scale (SAS) and Self-Rating Depression Scale (SDS) scores than the control group (both P<0.001).
-
Twenty-four studies were identified and confirmed that patients with dementia frequently resort to the ED near the end of life, frequently more than once in their last year of life.
-
Advance Care Planning (ACP) is a continuous process that enables individuals to discuss and document their preferences for future care in the event of terminal illness or incapacitation.
-
Regression analysis identified three different models as predictors of caregiver burden.
-
Kolb’s experiential learning theory has a positive impact on alleviating the caregiving burden and reducing anxiety and depression among family caregivers of dementia patients.
-
Daily informal care time was 0.5 hours higher in moderate compared to mild and 1.3h higher in severe compared to mild cognitive impairment.
-
People use advance directives to express preferences that direct their future care when they lack decision-making capacity.
-
The study found significant correlations between caregiver competence, QoL, and burden/stress with the QoL of individuals with dementia.
-
Apathy is a prevalent and persistent neuropsychiatric syndrome across many neurological disorders, significantly impacting both patients and caregivers.
-
Of 142 respondents, 53% supported, 10% were uncertain, and 37% opposed legalizing euthanasia for terminal illness with severe symptoms.
-
Participants with Lewy body dementia described losses associated with communication, continence, and energy leading to a progressive loss of independence.
-
Dementia is a progressive condition that gradually impairs cognitive function, memory, and daily living skills.
-
A total of 2301 patients completed an intake from January 2023 to March 2024.
-
The online SiD decision aid increased preparation for decision making about firearm access in this sample of ADRD caregivers in the United States.
-
Polypharmacy is an important healthcare issue, especially in elderly patients with dementia.
-
Study findings will reveal the feasibility of delivering an 8-week multidomain health education intervention for primary prevention of dementia in midlife and will provide preliminary evidence of mechanisms of change.
-
Phase 3 (NIH stage 1B) is a feasibility randomized controlled trial of the intervention versus the Health Education Program control.
-
Between Feb 24, 2021, and March 5, 2023, 377 dyads were randomly assigned (1:1), 189 to usual treatment and 188 to intervention.
-
Many individuals with advanced dementia die in hospital, despite preferring home death.
-
A collaborative dementia care program demonstrated significant financial benefit in a managed Medicare population.
-
Participants receiving CDCM showed significantly fewer behavioral and psychological symptoms (adjusted mean difference [AMD] in NPI score, -10.26 [95% CI, -16.95 to -3.58]; P = .003; Cohen d, -0.78 [95% CI, -1.09 to -0.46]), better mental health (AMD in SF-12 Mental Component Summary score, 2.26 [95% CI, 0.31-4.21]; P = .02; Cohen d, 0.26 [95% CI, -0.11 to 0.51]), and lower caregiver burden (AMD in BIZA-D score, -0.59 [95% CI, -0.81 to -0.37]; P Conclusions and relevance In this secondary analysis of a cluster randomized clinical trial, CDCM was associated with improved patient, caregiver, and health system-relevant outcomes over 36 months beyond the intervention period.
-
Enrollment in Medicare Advantage (MA) has been rapidly growing.
-
This study underscores the substantial prevalence of loneliness and social isolation among informal carers of individuals with dementia.
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.
- State-of-the-Art HCI for Dementia Care: A Scoping Review of Recent Technological Advances
- Comfort goal of care and end-of-life outcomes in dementia: A prospective study
- Filial Piety Under Pressure: A Qualitative Study of Dementia Caregiver Burdens in Rural China
- Sleep Quality of Persons with Dementia and Family Caregivers in Korean Americans: Wearable Technology to Study the Dyadic Association
- Care at the end of life for people with dementia living in a care home: a qualitative study of staff experience and attitudes
- Nursing home funding -- deal or no deal ? -- an Irish perspective
- Context, mechanisms and outcomes in end of life care for people with advanced dementia
- Institutional Special Needs Plans and End-of-Life Outcomes for Nursing Home Residents With Dementia
- Sense of Coherence and Caregiver Burden Among Informal Caregivers of People with Dementia in China: The Mediating Role of Coping Strategies