Results 101 to 110 of about 825,134 (282)

Shared Caregiving Responsibilities of Adult Siblings with Elderly Parents [PDF]

open access: yes
This paper uses a nonstructural, ordered discrete choice model to measure the effects of various parent and child characteristics upon the independent caregiving decisions of the adult children of elderly parents sampled in the 1982 and 1984 National ...
Steven Stern, Tennille J. Neuharth
core  

Survey nonresponse among informal caregivers: effects on the presence and magnitude of associations with caregiver burden and satisfaction

open access: yesBMC Public Health, 2016
Background Informal caregiving is becoming more relevant with current trends such as population ageing. However, little is known about nonconsent and nonresponse bias in caregiving research.
Marloes Oldenkamp   +4 more
doaj   +1 more source

Surviving the Storm: A Qualitative Study of Caregivers' Challenges in Family‐Based Treatment for Adolescent Anorexia Nervosa

open access: yesInternational Journal of Eating Disorders, EarlyView.
ABSTRACT Objective Family‐based treatment (FBT) is the recommended first‐line outpatient treatment for adolescent anorexia nervosa (AN) in Aotearoa New Zealand (NZ), but places substantial responsibility on parents/caregivers. Although caregiver burden in FBT is increasingly recognized internationally, in‐depth qualitative work situated in the NZ ...
Natasha Allen, Amy Kecher, Liesje Donkin
wiley   +1 more source

Perceived Barriers to Help‐Seeking for Eating Disorders Among Adults With Self‐Reported Eating Disorder Symptoms in Sweden

open access: yesInternational Journal of Eating Disorders, EarlyView.
ABSTRACT Objective Help‐seeking for eating disorders (EDs) remains low despite their burden and the importance of early intervention. This multimethod study examined perceived barriers to help‐seeking among adults with self‐reported ED symptoms in Sweden, a context underrepresented in prior help‐seeking research.
Anne‐Charlotte Wiberg   +3 more
wiley   +1 more source

Daily hemodialysis and caregivers burden [PDF]

open access: yesNephrology Dialysis Transplantation, 2011
Bolesław, Rutkowski, Ivan, Rychlik
openaire   +2 more sources

Dietary patterns in children with epilepsy: The role of household environment and clinical comorbidities

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective To evaluate dietary patterns in children with epilepsy and compare them with age‐ and sex‐matched healthy siblings living in the same household environment. Associations between clinical characteristics and dietary adequacy were also examined.
Ana Claudia Cândido Oliveira   +5 more
wiley   +1 more source

Core outcome set for quality of life of family caregivers of adults with epilepsy: A Delphi consensus study

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective Epilepsy significantly affects daily functioning and health‐related quality of life (HRQOL) of those living with the condition. Less is known about HRQOL of family caregivers of adults with epilepsy, yet the functioning of patients and caregivers is interlinked, and caregivers' unmet support needs are high.
Florien Boele   +10 more
wiley   +1 more source

Caregiving: A loving burden

open access: yesCancer Research, Statistics, and Treatment, 2023
Vandana Mahajan
doaj   +1 more source

Silence around SUDEP and its impact on caregivers of individuals with developmental and epileptic encephalopathies: An international survey

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Sudden Unexpected Death in Epilepsy (SUDEP) is the leading cause of epilepsy‐related mortality, particularly in individuals with Developmental and Epileptic Encephalopathies (DEEs). The goal of this work is to assess SUDEP‐related knowledge, information practices, emotional and psychological impact, and the use of preventive measures
José Ángel Aibar   +8 more
wiley   +1 more source

Caregiver burden, mental health, quality of life and self-efficacy of family caregivers of persons with dementia in Malaysia: baseline results of a psychoeducational intervention study

open access: yesBMC Geriatrics
Background The majority of persons with dementia (PWD) are mainly cared for by their family members in the home. Evidence is however scarce on family caregivers’ psychosocial burden and quality of life in Asian countries including Malaysia.
Hashima E. Nasreen   +9 more
doaj   +1 more source

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