Family caregivers' subjective experiences of satisfaction in dementia care: aspects of burden, subjective health and sense of coherence.
about
Compassion fatigue: an application of the concept to informal caregivers of family members with dementiaAn integrated review of interventions to improve psychological outcomes in caregivers of patients with heart failure.Diaries as research data in a study on family caregivers of people with Alzheimer's disease: methodological issues.Benefits of a poetry writing intervention for family caregivers of elders with dementia.Measuring the impact of caregiving on informal carers: a construct validation study of the CarerQol instrumentWell-being losses due to care-givingExperiences of end of life amongst family carers of people with advanced dementia: longitudinal cohort study with mixed methods.Psychometric properties and relations with coping and family strain of the Health Services and Caregiver Experience questionnaire (HSCE): an outcome measure of informal caregivers' experience for inpatient care in Italy.Caring for a child with autism spectrum disorder and parents' quality of life: application of the CarerQol.Family caregivers' assessment of symptoms in persons with dementia using the GBS-scale: differences in rating after psychosocial intervention--an 18-month follow-up study.Do partners of patients with chronic heart failure experience caregiver burden?Spouses, adult children, and children-in-law as caregivers of older adults: a meta-analytic comparison.Characteristics and mental health of Hispanic dementia caregivers in New York City.How caregivers and workers fared in Cash and Counseling.Dyads affected by chronic heart failure: a randomized study evaluating effects of education and psychosocial support to patients with heart failure and their partners.Identifying family members who are likely to perceive benefits from providing care to a person with a primary malignant brain tumor.The influence of day care centres designed for people with dementia on family caregivers - a qualitative study.Gender differences in caregiving among family - caregivers of people with mental illnesses.Factors Predicting Bereaved Caregiver Perception of Quality of Care in the Final Week of Life: Implications for Health Care ProvidersBurden of informal care giving to patients with psychoses: a descriptive and methodological studyExploring the effectiveness of an internet-based program for reducing caregiver distress using the iCare Stress Management e-Training Program.Telephone-delivered psychoeducational intervention for Hong Kong Chinese dementia caregivers: a single-blinded randomized controlled trialPsychosocial aspects of children and families of children treated with automated peritoneal dialysis.Supporting activity engagement by family carers at home: maintenance of agency and personhood in dementia.Effectiveness of online cognitive behavioral therapy on family caregivers of people with dementia.Social support, caregiving, and aging.Long-term effects of a dyadic psycho-educational intervention on caregiver burden and morbidity in partners of patients with heart failure: a randomized controlled trial.The family caregiver experience - examining the positive and negative aspects of compassion satisfaction and compassion fatigue as caregiving outcomes.Burden, emotional distress and quality of life among informal caregivers of lung cancer patients: An exploratory study.Patterns of change and stability in caregiver burden and life satisfaction from 1 to 2 years after severe traumatic brain injury: A Norwegian longitudinal study.Is sense of coherence helpful in coping with caregiver burden for dementia?Beyond Strain: Personal Strengths and Mental Health of Mexican and Argentinean Dementia Caregivers.The health of caregivers for children with disabilities: caregiver perspectives.Influence of home care services on caregivers' burden and satisfaction.General practitioners' perceptions of the stigma of dementia and the role of reciprocity.Family caregivers' assessments of caring for a relative with dementia: a comparison of urban and rural areas.The experiences of working carers of older people regarding access to a web-based family care support network offered by a municipality.Caregiving in Dementia and its Impact on Psychological Functioning and Health-Related Quality of Life: Findings from a Colombian Sample.The Association of Satisfaction and Perceived Burden With Anxiety and Depression in Primary Caregivers of Dependent Elderly Relatives.Attitudes to aging in older carers - do they have a role in their well-being?
P2860
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P2860
Family caregivers' subjective experiences of satisfaction in dementia care: aspects of burden, subjective health and sense of coherence.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Family caregivers' subjective ...... health and sense of coherence.
@en
Family caregivers' subjective ...... health and sense of coherence.
@nl
type
label
Family caregivers' subjective ...... health and sense of coherence.
@en
Family caregivers' subjective ...... health and sense of coherence.
@nl
prefLabel
Family caregivers' subjective ...... health and sense of coherence.
@en
Family caregivers' subjective ...... health and sense of coherence.
@nl
P2860
P1476
Family caregivers' subjective ...... health and sense of coherence.
@en
P2093
Signe Andrén
Sölve Elmståhl
P2860
P304
P356
10.1111/J.1471-6712.2005.00328.X
P577
2005-06-01T00:00:00Z