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首页> 外文期刊>BMC Neurology >Emergence and evolution of social self-management of Parkinson’s disease: study protocol for a 3-year prospective cohort study
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Emergence and evolution of social self-management of Parkinson’s disease: study protocol for a 3-year prospective cohort study

机译:帕金森病社会自我管理的出现与演变:3年前瞻性队列研究的研究议定书

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Background Parkinson’s disease affects facial, vocal and trunk muscles. As symptoms progress, facial expression becomes masked, limiting the person’s ability to communicate emotions and intentions to others. As people with the disease live and reside in their homes longer, the burden of caregiving is unmitigated by social and emotional rewards provided by an expressive individual. Little is known about how adults living with Parkinson’s disease manage their social lives and how an inability to be emotionally expressive can affect social connections and health. Because social networks have been shown to be crucial to the overall well-being of people living with chronic diseases, research is needed on how expressive capacity affects life trajectories and health. Methods/Design The overall objective is to understand the emergence and evolution of the trajectories of the self-management of the social lives of people living with Parkinson’s disease. The central hypothesis is that expressive capacity predicts systematic change in the pattern of social self-management and quality of life outcomes. The specific aims of this 3-year longitudinal study of 120 people with the disease and a maximum of 120 care partners are: 1) characterize social self-management trajectories over a 3-year period; 2) estimate the degree to which expressive nonverbal capacity predicts the trajectory; and 3) determine the moderating effect of gender on the association between expressive capacity and change in social self-management. Each participant will be assessed 14 times to detect rapid and non-linear changes in social participation and management of social activities; social network; and social comfort, general health and well-being. Discussion This project will provide evidence to guide the development of interventions for supporting social integration of those living with Parkinson’s disease, thus leading to improved overall health. It focuses on the novel construct of social self-management and known factors—expressive capacity and gender—that contribute to stigmatization. The repeated measures design detects triggers of rapid changes in social and health outcomes.
机译:背景帕金森病影响面部,声带和躯干肌肉。随着症状进展,面部表情变得掩盖,限制了对他人传达情感和意图的人的能力。随着疾病的人们生活和居住在家园的时间更长,护理的负担因表达个人提供的社会和情感奖励而无意义。众所周知,帕金森病的成年人如何管理他们的社会生命以及如何在情感上表达如何影响社会联系和健康。由于社会网络已被证明对患有慢性疾病的人们的整体福祉至关重要,因此需要研究表达能力如何影响生命轨迹和健康的研究。方法/设计整体目标是了解帕金森病的社会生活自我管理轨迹的出现和演变。中央假设是表现力能力预测社会自我管理模式和生活质量结果的系统变化。这项3年纵向研究的具体目标是120名患有疾病的120人和最多120名护理伙伴有:1)在3年期间,表征社会自我管理轨迹; 2)估计表达非语言容量预测轨迹的程度; 3)确定性别对表现能力与社会自我管理变革之间的关联的调节效果。每位参与者将被评估14次以检测社会参与和社会活动管理的快速和非线性变化;社交网络;和社会舒适,一般健康和福祉。讨论该项目将提供证据,以指导支持支持与帕金森病的社会融合的干预措施,从而提高整体健康状况。它侧重于社会自我管理和已知因素表达能力和性别的小说 - 有助于侮辱。重复的措施设计检测到社会和健康结果的快速变化的触发。

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