A one-year randomized controlled psychosocial intervention study among family carers of dementia patients - Effects on patients and carers

被引:40
|
作者
Ulstein, Ingun D. [1 ,2 ,3 ]
Sandvik, Leiv [4 ]
Wyller, Torgeir Bruun [2 ]
Engedal, Knut [1 ,2 ,3 ]
机构
[1] Ullevaal Univ Hosp, Dept Geriatr Med, Norwegian Ctr Dementia Res, NO-0407 Oslo, Norway
[2] Univ Oslo, Ullevaal Univ Hosp, Dept Geriatr Med, Oslo, Norway
[3] Innlandet Hosp Trust, Res Ctr Old Age Psychiat Res, Ottestad, Norway
[4] Ullevaal Univ Hosp, Clin Res Ctr, NO-0407 Oslo, Norway
关键词
dementia; burden of care; psychosocial intervention; relatives' stress scale; neuropsychiatric inventory; NURSING-HOME PLACEMENT; RELATIVE STRESS SCALE; ALZHEIMERS-DISEASE; CAREGIVERS; BURDEN; SYMPTOMS; RISK;
D O I
10.1159/000110740
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objective: To test the effect of a short-term psychosocial intervention programme for family carers of patients with dementia and identify characteristics of carers and patients that responded positively. Methods: The study was a multicentre randomized controlled trial. Carers of 180 patients suffering from dementia recruited at 7 memory clinics at geriatric or psychiatric departments participated in the study. Carers of the intervention group were educated about dementia and in 6 group meetings taught how to use structured problem-solving. The control group received treatment as usual. The effect on patients was measured with the Neuropsychiatric Inventory and on carers with the Relatives' Stress Scale (RSS). Results: The intention-to-treat efficacy analysis included 171 carer/patient dyads. The intervention did not have any effect on the primary outcome variables. The burden measured by the RSS increased in both groups; however, more carers of the control group converted from a low-burden group to a medium- or high-burden group after 4.5 months. In a subgroup analysis we found a statistically significant difference in the Neuropsychiatric Inventory score in favour of the intervention group among female patients. Conclusion: The predominately negative result of this study emphasizes the need of individually tailored interventions for carers and the use of narrow inclusion criteria when performing group-based interventions, such as the extent of burden as well as gender and kinship. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:469 / 475
页数:7
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