关于唐氏综合症患者健康状况的护理人员访谈。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Mary Witt, Kavita Krell, Stephanie L Santoro
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引用次数: 0

摘要

患有唐氏综合症(DS)的人有共同发生的医疗条件。需要研究照顾者如何理解、解释和回答有关他们患有退行性残疾的儿子或女儿的健康问题,以指导发展一种衡量患有退行性残疾的儿童和青少年健康状况的措施。我们对年龄在0至21岁的DS患者的照顾者进行了1小时的虚拟认知访谈,内容涉及我们起草的身体、心理和社会健康调查项目,使用了改进的“大声思考”方法和探针。除了使用他们的反馈来迭代地改进我们的调查,在这份手稿中,我们描述了来自照顾者的反馈的主题,并总结了调查项目的变化。对42名退行性痴呆患者的照顾者进行四轮认知访谈,共40次访谈。认知访谈的主题包括:尽可能使用最简单的短语,关注现在,在术语上保持对话,指明项目指的是谁或比较组是谁,等等。护理人员访谈提供了信息,并使我们对调查项目进行了修改。出现的主题对其他研究人员在遗传综合征人群中进行调查有帮助。试验注册:NCT04631237。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Caregiver Interviews Regarding Health in Down Syndrome.

Individuals with Down syndrome (DS) have co-occurring medical conditions. Research on how caregivers understand, interpret, and answer questions about the health of their son or daughter with DS is needed to guide the development of a measure of the health status of children and adolescents with DS. We conducted 1-h virtual cognitive interviews of caregivers of individuals aged 0 to 21 with DS about our drafted survey items on physical, mental, and social health using a modified "think-aloud" approach with probes. In addition to using their feedback to iteratively refine our survey, in this manuscript we describe the themes of feedback from caregivers and summarize survey item changes. Four rounds of cognitive interviews for a total of 40 interviews of 42 caregivers of individuals with DS were completed. Cognitive interview themes included: using the easiest phrase possible, focusing on the present, being conversational in terminology, and specifying who items refer to or who comparison groups are, among others. Caregiver interviews were informative and led us to make modifications to our survey items. Themes emerged which hold use to other researchers conducting surveys in populations with genetic syndromes. Trial Registration:NCT04631237.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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