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caregiver
195 studies tagged caregiver, dated 1982-07-16 to 2026-10-29. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Elder Caregiving in Southeast Asia: A Systematic Review of Cultural Norms, Care Burdens, Carer Support and Policy Gaps 2026-10-29
- Beyond “Denial”: Understanding and Responding to Help-Refusal in Dementia 2026-10-26
- Caregiving experiences of older-adult informal family caregivers for older adults with comorbid dementia and physical disability: A qualitative study using the caregiving stress-process model 2026-10-14
Studies
195 studies carry this tag.
Date range
1982 to 2026
Top journals
- The Gerontologist 15
- Research Square 14
- International journal of geriatric psychiatry 9
- Aging & mental health 8
- Dementia (London, England) 6
105 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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Forty-eight studies from ten Southeast Asian countries were reviewed.
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Evidence for interventions that reduce refusal is strongest for music during personal care and modified bathing methods, with some support for positive communication and person-centred approaches, though quality is generally low and few studies involve family caregivers in community settings.
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Five core themes and fifteen corresponding sub-themes were extracted from interview transcripts: (1) Structural caregiving context, including family structural constraints, the influence of filial piety culture, and insufficient aged-care supply; (2) Multiple caregiving stressors, covering primary care burden, independent care decision-making pressure, restricted social engagement, and intra-family conflicts; (3) Limited buffering support resources, involving inadequate formal care services, insufficient informal assistance from relatives, and individual psychological coping strategies; (4) Negative caregiving experiences, including persistent physical exhaustion and sustained emotional depletion; (5) Dual perceptions of caregiving outcomes, consisting of emotional gains from kinship bonding, resistance to institutional care, and long-term anxiety about future care arrangements.
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People from UK South Asian communities experience barriers to accessing dementia care.
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Dementia dyads experience substantial informational, emotional, and practical support needs in the early stages of MCI and AD/ADRD.
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16/100
Depressive and anxiety symptoms were more pronounced among caregivers with longer caregiving duration (p = 0.01; p = 0.001) and those living with the care recipient (p = 0.04; p = 0.02).
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Our study delivers ambivalent results for the efficacy of care management for caregivers.
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Dementia public stigma was associated with education, dementia knowledge, media exposure, chronic diseases, and contact experience with people living with dementia.
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Three interrelated themes emerged: relational foundations of caregiving, multidimensional struggles of caregiving, and benefits of caregiving.
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Our results showed that caregiving burden was negatively associated with the sense of ability..
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Older adults in senior living communities (SLCs) often face barriers to maintaining emotional well-being and family ties.
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Drama therapy is in an accelerated growth phase, with substantial scholarly expansion expected over the next two decades.
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Caregiver narratives were predominantly negative (89.3% of posts; mean valence - 0.46), with interpretable structure.
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Four main themes emerged from the data: 1) the unseen challenges of caregiving; 2) knowledge and experiences lead to stronger self-confidence; 3) the power of peer influence on caregiving; and 4) pursuing better support for carers.
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The culturally adapted CSP enhanced self-efficacy among Chinese Australian carers of people with dementia, but not carer burden, quality of life and approach to dementia care.
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Although caregivers demonstrated resilience and adaptive coping, YOD caregiving in Singapore remained constrained by limited access to visible, tailored, and age-appropriate support.
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Caregiving for older adults with dementia in Northern Ethiopia is a totalizing and demanding experience that profoundly affects caregivers’ lives.
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We included 23 studies with qualitative (73.9%) or quantitative/mixed-methods (26.1%) designs.
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Persons with dementia (PWD) and their care partners experience multidimensional care transitions across the illness trajectory.
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Dementia is a growing global concern, with informal caregivers, typically unpaid family members or friends, providing essential support to those living with the condition.
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Wearable devices may facilitate the measurement and treatment of specific BPSD, as well as reduce caregiver burden.
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A total of 228 articles were screened at the title and abstract levels, and 120 full-text articles were assessed for eligibility. 23 eligible studies were included in the narrative synthesis.
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An initial database search yielded 3,977 studies of which 22 were included in this review.
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Interventions for family caregivers of individuals with Alzheimer's disease and related dementias (ADRD) incorporate diverse elements, but drivers of success are unclear.
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Social connectedness is important for maintaining cognitive function and cognitive health in older age.
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The employed family caregivers juggle caregiving and work responsibilities constantly, highlighting a growing concern for their financial and professional well-being.
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Baseline assessments were conducted on 133 family caregivers of veterans living with dementia.
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The mean age of the patients was 73.1 ± 11.7, and the time since diagnosis was 3.9 ± 3.1 years; 64.8% had Alzheimer's type dementia, and 53.4% (n = 47) had mild dementia.
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Contrary to expectations, pain and mental health measures for PLWAD displayed a trend toward negative correlation with their hair cortisol levels.
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43/100
Out-of-pocket costs of dementia care were collected via a web-based weekly survey for up to 18 months.
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50/100
The PWD and ICG interviews provided insight into the positive impacts of VP, challenges of VP, program barriers, program facilitating factors, and suggestions for future improvement for the OSCC55 + VPs.
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Four major themes emerged: forgetting to eat, developing food aversions, strong preferences for sweets and weight changes.
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54/100
The result of the validity test of the CNA-D instrument, Indonesian version, obtained a high value for content validity.
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The mean score for affiliate stigma of dementia family caregivers was 48.09 ± 16.38 (range: 22-86).
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Family caregivers of older adults living with severe dementia had the highest baseline Zarit Burden Interview (ZBI) score of 27.7 which decreased to 25.0 (p < .05); family caregivers of those living with moderate dementia had a baseline ZBI score of 24.3 which decreased to 20.4 (p < .01); and family caregivers of those living with mild dementia had the lowest baseline ZBI score of 21.0, which decreased to 18.0 (p < .01).
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People with early-stage AD and their spousal caregivers provided support to each other often.
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A total of 5971 titles were reviewed and 60 studies were included in the analysis, 36 RCTs and 24 observational studies.
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This cross-sectional study explores caregivers' perceptions of feeding/eating difficulties in persons living with dementia, their support provisions, and the associated burdens.
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The predictors of the Social Loneliness factors were as follows; 1) perceived social support (R2 = 0.33): Neuroticism (β= 0.353), depression (β= 0.205), and perceived health (β= 0.133); 2) social participation (R2 = 0.24): Conscientiousness (β= -0.344) and Extraversion (β= -0.263); 3) use of communication technologies (R2 = 0.44): age (β= 0.409), type of cohabitation (β= 0.331), cognitive reserve (β= -0.303), and Conscientiousness (β= -0.247); all p < 0.05.
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50/100
Adjusted for functional impairments and sociodemographic variables, neuropsychiatric symptoms were associated with more caregiver burden (p < 0.001).
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This review describes associations between dementia and loneliness on the neurobiological and epidemiological levels according to the recent body of literature.
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This is the first study adopting the multiphase optimisation strategy to identify the most active and engaging components of a psychological intervention for caregivers of patients with dementia.
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Testing interventions in real-world settings requires fidelity monitoring to ensure implementation integrity.
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79/100
Caregivers often prioritize the needs of the care recipient and neglect their own health needs.
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The treatment group had no EM after intervention completion (assessed at 3-month follow-up), a significantly lower rate than the control group (treatment = 0%, control = 23.1%, p = 0.010).
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Breakdown (coded as 0) was associated with caregivers changing topic (median = -11.45, 95% credibility interval [CrI; -24.34, -4.37]), ignoring (median = -11.49, 95% CrI [-24.49, -4.72]), giving commands (median = -10.74, 95% CrI [-24.22, -3.38]), and taking over the task (median = -4.06, 95% CrI [-7.28, -1.77]).
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Average caregiver burden on the ZBI was 36.1 (SD = 14.6; range = 12-58).
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We included 60 AD individuals-caregivers dyads.
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Four major themes emerged: Methods of Support, Cultural Expectations and Varying Family Contributions, Lack of Self-Care, and Awareness.
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48/100
Three themes were identified; 1) intersectionality in the Korean American caregiver experience, 2) complex family dynamics, and 3) dementia care barriers and caregiver support needs.
From across this tag
10 of the 195 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.
- Social Frailty Is Associated with Physical Functioning, Cognition, and Depression, and Predicts Mortality
- Caregiver Burden and Quality of Life Across Alzheimer's Disease Severity Stages
- Competing crises: COVID‐19 countermeasures and social isolation among older adults in long‐term care
- Cohort Profile: The Longitudinal Aging Study Amsterdam
- Mediators of burden and depression in dementia family caregivers: Kinship differences
- Dyadic Hair Cortisol Self-Collection Procedure
- Association Between Family Caregiver Burden and Affiliate Stigma in the Families of People with Dementia
- Change in Indices of Distress Among Latino and Anglo Female Caregivers of Elderly Relatives With Dementia: Site-Specific Results From the REACH National Collaborative Study
- Family caregiving in dementia: the Asian perspective of a global problem
- The relationship between social isolation and anxiety in people with cognitive impairment in the United States