Objective. To investigate predictors of carer burden in Alzheimer's disease (AD). Design. Two cohorts were formed, one comprising AD patients, the other comprising their primary carers. The relationship of patient and carer variables to carer burden was investigated. Setting. An urban hospital memo
Dementia carer education and patient behaviour disturbance
✍ Scribed by Robert F. Coen; Ciaran A. O'Boyle; D. Coakley; Brian A. Lawlor
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 83 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0885-6230
No coin nor oath required. For personal study only.
✦ Synopsis
Objective. To evaluate the impact of a dementia Carer Education Programme on carer quality of life (QoL), burden, and well-being.
Design. Single group before±after intervention study. The group was subdivided by perceived status postprogramme for intragroup analysis.
Setting. Hospital memory clinic.
Participants. Convenience sample of 32 dementia carers.
Intervention. Eight weekly 2 h education and support sessions run by a psychogeriatric clinical team.
Measures. Pre-programme and 6 months post-programme data were obtained. Measures included individually perceived QoL, burden, well-being, managing problem behaviour, appraisal of social support, knowledge of dementia, and perception of the programme. Patients were characterized in terms of cognition, behaviour disturbance and functional status.
Results. Twelve carers reported their situation post-programme as better', 12 as worse', and four as no change'. There were no signi®cant baseline dierences. For better/no change' carers the only signi®cant change over time was increased knowledge about dementia. For worse' carers knowledge also increased, but there was evidence of poorer QoL, increased burden, a poorer appraisal of social support, and increased patient behaviour disturbance. Only patient behaviour disturbance signi®cantly discriminated no change/better' from `worse' carers (F 4.08, p 0.055).
Conclusions. The programme increased carers' knowledge about dementia, but had no signi®cant impact on QoL, burden, or well-being. Increased patient behaviour disturbance appeared to be a major factor when the carer's situation worsened over time. Despite high carer satisfaction the ecacy of a group-based education approach to the management of behaviour disturbance in dementia appears limited. More intensive or individually tailored interventions may be necessary alternatives.
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