Identification of psychoeducation needs and an intervention response for pre-symptomatic Huntington's disease.

IF 1.5 Q4 GENETICS & HEREDITY
Cathy Gluyas, Lisa Mottram, Rosanne Gibb, Julie Stout
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引用次数: 1

Abstract

People who are aware that they are gene-positive for Huntington's disease (HD) may face an array of personal, relationship, social, financial and employment challenges prior to the onset of the disease. These challenges have been associated with increased psychological problems such as anxiety and depression. Information and support for people with pre-symptomatic HD is indicated, but there is a scarcity of research and service models to inform psychological interventions. We trialled an intervention strategy involving psychoeducation forums designed specifically for pre-symptomatic HD. In phase I of the study, we asked people with pre-symptomatic HD to identify their uppermost needs for information. Phase II involved the delivery of this information via a series of forums. The forums also provided an opportunity for interaction among the participants. Three forums were attended by 88 people with pre-symptomatic HD and significant others. Analysis of post-forum feedback questionnaires indicated high levels of satisfaction with the forums' structure, content and relevance, and notably, the pre-symptomatic specificity of focus. Additional qualitative data from recordings of forum discussion groups revealed that participants greatly valued the opportunity to meet similar others, and share their concerns and strategies for addressing these concerns. There was an abundance of requests for more forums on a wide range of relevant topics. It is recommended that this model of intervention may be of value for implementation in other HD services or community groups.

Abstract Image

对症状前亨廷顿舞蹈病的心理教育需求的识别和干预反应。
意识到自己是亨廷顿舞蹈病(HD)基因阳性的人可能在发病前面临一系列个人、关系、社会、经济和就业方面的挑战。这些挑战与焦虑和抑郁等心理问题的增加有关。有必要为症状前HD患者提供信息和支持,但缺乏研究和服务模式来为心理干预提供信息。我们试验了一种干预策略,包括专门为症状前HD设计的心理教育论坛。在研究的第一阶段,我们要求患有症状前HD的人确定他们对信息的最大需求。第二阶段涉及通过一系列论坛提供这些信息。论坛也为与会者之间的互动提供了机会。88名症状前HD患者和其他重要患者参加了三个论坛。对论坛后反馈问卷的分析表明,对论坛的结构、内容和相关性非常满意,特别是对焦点的症状前特异性非常满意。来自论坛讨论组记录的其他定性数据显示,参与者非常重视与相似的人见面的机会,并分享他们的关注点和解决这些关注点的策略。有很多人要求就广泛的相关主题举办更多的论坛。我们建议,这种干预模式可能对其他卫生署服务或社区团体的实施有价值。
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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