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The Impact of Experience with a Family Member with Alzheimer’s Disease on Views about the Disease across Five Countries

机译:患有阿尔茨海默氏病的家庭成员的经历对五个国家对该疾病的看法的影响

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The objective of this paper is to understand how the public’s beliefs in five countries may change as more families have direct experience with Alzheimer’s disease. The data are derived from a questionnaire survey conducted by telephone (landline and cell) with 2678 randomly selected adults in France, Germany, Poland, Spain, and the United States. The paper analyzes the beliefs and anticipated behavior of those in each country who report having had a family member with Alzheimer’s disease versus those who do not. In one or more countries, differences were found between the two groups in their concern about getting Alzheimer’s disease, knowledge that the disease is fatal, awareness of certain symptoms, and support for increased public spending. The results suggest that as more people have experience with a family member who has Alzheimer’s disease, the public will generally become more concerned about Alzheimer’s disease and more likely to recognize that Alzheimer’s disease is a fatal disease. The findings suggest that other beliefs may only be affected if there are future major educational campaigns about the disease. The publics in individual countries, with differing cultures and health systems, are likely to respond in different ways as more families have experience with Alzheimer’s disease.
机译:本文的目的是了解随着越来越多的家庭对阿尔茨海默氏病有直接的经验,五个国家的公众观念可能会发生变化。数据来源于通过电话(座机和手机)对法国,德国,波兰,西班牙和美国的2678名随机选择的成年人进行的问卷调查。该论文分析了每个国家中报告有家庭成员患有阿尔茨海默氏病的人的信念和预期行为。在一个或多个国家/地区中,发现两组之间在关注阿尔茨海默氏病,对这种疾病具有致命性的认识,对某些症状的认识以及对增加公共支出的支持等方面存在差异。结果表明,随着越来越多的人与患有阿尔茨海默氏病的家庭有经验,公众通常会更加关注阿尔茨海默氏病,并且更有可能认识到阿尔茨海默氏病是致命性疾病。研究结果表明,只有未来有关于这种疾病的大型教育运动,其他信念才会受到影响。随着越来越多的家庭经历过阿尔茨海默氏病的经验,各个国家和地区的公民具有不同的文化和医疗体系,他们可能会采取不同的应对方式。

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