𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Canadian Alzheimer's disease caregiver survey: baby-boomer caregivers and burden of care

✍ Scribed by Sandra E. Black; Serge Gauthier; William Dalziel; Ron Keren; Jane Correia; Huong Hew; Carin Binder


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
110 KB
Volume
25
Category
Article
ISSN
0885-6230

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Objective

Alzheimer's disease (AD) burdens not only the person, but also the person's caregiver(s). This burden has been linked to negative health effects for caregivers. To that end, a survey of Canadian caregivers of persons with AD/other dementias was conducted to investigate the social, physical, psychological and financial impact of AD and/or dementia‐related conditions on caregivers' quality of life.

Methods

A web‐based survey, the Canadian Alzheimer's Disease Caregiver survey, was made available through the Canadian Alzheimer's Society website and 50plus.com, an internet portal for baby boomers (BB) (people aged 50 years or older), as well as through HarrisDecima Research's e‐Vox panel. A total of 398 individuals completed the survey between 15 September and 5 November 2006.

Results

Of the 398 total respondents, 221 were identified as baby boomers who provided care to an individual with AD/dementia. Respondents identified several areas of burden of care. These included negative effects on emotional health (such as increased depression, more stress and greater fatigue), financial costs and a need to change a working situation (e.g. by retiring early, reducing work hours or refusing a promotion).

Conclusion

Caregivers of persons with AD/related dementia face important social, physical, psychological and financial pressures. These negatively affect the quality of life of caregivers with a significant increased burden being placed on live‐in caregivers versus caregivers who do not co‐reside with their care recipients. Interventions that address these pressures will not only improve the health and well‐being of caregivers, but likely also the care of persons with AD/dementia. Copyright © 2009 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Effectiveness of a psychoeducational int
✍ Manuel Martín-Carrasco; Manuel Franco Martín; Carmelo Pelegrín Valero; Pedro Roy 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB 👁 2 views

## Abstract ## Objectives Caregivers of patients with Alzheimer's disease (AD) experience physical and psychological stress due to the caring experience. This study evaluated the benefits of a Psychoeducational Intervention Program (PIP) on caregiver burden in southern Europe. ## Methods A multi

The Caregiver Activity Survey (CAS): dev
✍ Kenneth L. Davis; Deborah B. Marin; Robert Kane; Donald Patrick; Elaine R. Peski 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 158 KB 👁 3 views

## Background: Most instruments that measure the impairments associated with alzheimer's disease assess symptom severity. little attention has been paid to the illness's impact on the time formal and informal caregivers spend caring for alzheimer's individuals. a tool that measures the time spent c

Alzheimer’s disease: usefulness of the F
✍ Silvia Rossi Ferrario; Peter Vitaliano; Anna Maria Zotti; Emanuela Galante; Robe 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 60 KB 👁 3 views

## Abstract ## Objectives The economic and psychosocial impacts of Alzheimer's disease (AD) on caregivers are so well documented that they have stimulated socioeconomic regulations that are international in scope. In Italy caregivers have the right to receive economic and psychosocial aid. However

Cognitive function and caregiver burden:
✍ Stéphanie Rivière; Sophie Gillette-Guyonnet; Sandrine Andrieu; Fati Nourhashemi; 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB 👁 1 views

## Abstract ## Background Patients with Alzheimer's disease (AD) commonly develop aversive feeding behaviours. These behaviours lead to weight loss and frequently to physicians using tube feeding. Little is known about factors correlated with feeding difficulties during AD. ## Objective To inves

The Caregiver Activity Survey (CAS): lon
✍ Deborah B. Marin; Micheline Dugue; James Schmeidler; Jennifer Santoro; Judith Ne 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 85 KB 👁 2 views

Family members incur substantial \_nancial costs during the course of caring for an individual with Alzheimer|s disease[ Much of this cost is associated with time spent in caregiving tasks\ including supervision and communication with the patient\ and assisting with activities of daily living[ We ha

Burden, perceived health status, and moo
✍ Pablo Martinez-Martin; Susana Arroyo; Jose Manuel Rojo-Abuin; Carmen Rodriguez-B 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB

## Abstract The objective of this study is to describe the characteristics of the caregivers of patients with Parkinson's disease (PD) and to analyze the association between these characteristics and caregiver burden, perceived health and mood status, and identify their predictors. A multicenter, n