Results 351 to 360 of about 989,120 (394)
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Differences between caregivers and noncaregivers in psychological health and physical health: a meta-analysis.

Psychology and Aging, 2003
Providing care for a frail older adult has been described as a stressful experience that may erode psychological well-being and physical health of caregivers.
M. Pinquart, S. Sörensen
semanticscholar   +1 more source

Caregiver Burden or Caregiver Gain?: Respite for Family Caregivers

Journal of Psychosocial Nursing and Mental Health Services, 2009
Many caregivers of older family members do not realize the need for respite until their own health begins to deteriorate. The mental, emotional, and physical stress of caring for a family member can seem overwhelming. Creative options for respite care are emerging, but there are barriers to effective use of these programs.
Pamela R. Cangelosi, Jeanne M. Sorrell
openaire   +3 more sources

Caregiving and Caregivers: Concepts, Caregiving Models, and Systems

2023
The increasing number of care-dependent people leads to a high demand of economic burden for most healthcare systems. This has also led to an increase on the demand for informal care, usually assumed by a family member or a significant other. Informal care is the provision of unpaid care or support to others who need help or who are unable to care for ...
openaire   +2 more sources

Resilience in Caregivers: A Systematic Review

The American journal of hospice & palliative care, 2019
Background: Resilience is a multidimensional construct that explains why people facing the consequences of adversity and stress can have a positive outcome, emphasizing adjustment to experiences that are perceived as threatening.
Carolina Palacio G   +3 more
semanticscholar   +1 more source

Family Caregiving in Bipolar Disorder: Caregiver Consequences, Caregiver Coping Styles, and Caregiver Distress

International Journal of Social Psychiatry, 2008
Aims: This study investigated the consequences caregivers of outpatients with bipolar disorder are confronted with, the distress they experience and their coping styles. Methods: Caregivers ( n = 115) were asked to complete the Involvement Evaluation Questionnaire (IEQ) to measure caregivers' consequences, the Utrecht Coping List (UCL) to measure ...
Goossens, P.J.J.   +3 more
openaire   +4 more sources

Caregiver burden for informal caregivers of patients with dementia: A systematic review.

International Nursing Review, 2015
BACKGROUND Dementia is an irreversible illness. The caregiver is expected to assume increased responsibility as the condition of the person with dementia declines.
Chia-Yi Chiao, H-S Wu, C. Hsiao
semanticscholar   +1 more source

Caregiving and Caregivers [PDF]

open access: possible, 2012
Remarkable strides have been made in the treatment of HIV/AIDS, yet a considerable proportion of those infected with the virus may continue to require care. Those with cognitive deficits, those aging into a second decade of HIV infection, and those struggling with debilitating physical and mental symptoms may need at home caregiving.
openaire   +1 more source

The Representations of Caregiving in Informal Caregivers

The Family Journal
Informal caregiving is usually deemed stressful and an activity leading to worsening life conditions. Nevertheless, recent studies have suggested the possibility for an informal caregiver to simultaneously experience both positive and negative feelings, identifying in the positive assets the merit of raising resilience and a sense of self ...
Francesca Tricarico   +2 more
openaire   +2 more sources

Impact of caregiving on Finnish family caregivers

Scandinavian Journal of Caring Sciences, 2011
Numerous studies have examined the caregiver burden that family caregivers often experience. However, caregiving situations may also include positive elements that have recently received greater research attention.The aim was to examine the positive value and negative impact of caregiving for the family caregiver.Caregiving experience was measured with
Maisa Toljamo   +2 more
openaire   +2 more sources

Caregiver Role Appraisal and Caregiver Tasks as Factors in Ending Caregiving

Journal of Aging and Health, 1994
This study focuses on factors related to why people with primary responsibility for providing care to ADL-impaired elderly persons ended their caregiving roles. Data are from the 1982 National Long-Term Care Survey and the Informal Caregiver Survey. Variables reflecting characteristics of care recipients and caregivers, caregiver role responsibilities,
Judith D. Kasper   +2 more
openaire   +3 more sources

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