Together the integrated aspects constituting the model of care based upon the New York University Caregiver Intervention (NYUCI) were shown to enhance caregivers’ quality of life in this three-year study.
This qualitative study explored the hospitalization journey of people with dementia in Taiwan from their family caregivers' perspectives. Semi-structured interviews with nine caregivers revealed three key themes: care model tensions, psychological/moral burdens, and environmental conflicts. Hospitalization exposes syst...
Pei-Chao Lin, P. Chou, Chun-Ju Yen et al.· Journal of gerontological so...· 0 citations
Caring for a family member with dementia places long‐term emotional, physical, and social strain on primary caregivers. Although extensive research has examined the caregiving phase, relatively few studies have explored caregivers' recovery experiences following bereavement, particularly in Chinese cultural contexts.
Wen-Ying Chang, Shan-Mei Chang, W. Yen et al.· International Journal of Ger...· 0 citations
Background: Slowing the progression of dementia and maintaining mental and social health and well-being are important aspects of health and healthcare for people living with dementia (PLwD). Relationships with family caregivers and unique caregiver insights are also important aspects of the health and well-being of PLw...
Michelle D. Hand, Megumi Inoue, Li-Mei Chen et al.· Geriatrics· 0 citations
Children with special needs often require continuous care, supervision, and specialized interventions to support their development and daily functioning. Consequently, primary caregivers play a vital role in meeting their children's physical, emotional, educational, and therapeutic needs. Although caregiving can be rew...
Jayssamae S. Veloso, Ezra Shiene O. Felipe, Christhoffer P. Lelis· International journal of res...· 0 citations
Background: The progressive loss of autonomy in persons with dementia (PwD) creates a substantial, multi-faceted burden on their informal caregivers. Beyond instrumental support, caregivers require dedicated tools for disease comprehension and self-care. Unmet emotional and informational needs across the disease trajec...
Belén Montes Del Río, Nuria Berga Quintana, Noemí Cerulla Torrente et al.· International Journal of Int...· 0 citations
The growing population of people living with Alzheimer's disease and related dementias (ADRD) has increased the demand for informal care by family members and friends. While a growing number of studies about ADRD caregiving have engaged caregivers from diverse racial, ethnic, and/or sexual and gender minority backgroun...
Joel G. Anderson, N. M. Dowling, J. Flatt· American Journal of Alzheime...· 0 citations
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