whānau毛利人照顾自闭症谱系幼儿的经历

IF 1.6 Q2 ETHNIC STUDIES
Jessica Tupou, Chevelle Ataera, Hannah Waddington
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引用次数: 0

摘要

这项混合方法研究旨在探索毛利人父母和whānau(家庭)照顾年幼自闭症儿童的经历和目标。数据是通过rōpúkō; rero(焦点小组)和在线问卷收集的,共有33名父母和whānau参与了至少一个阶段的研究。反射主题分析用于分析rōpúkō; rero数据,研究结果用于为在线问卷的设计提供信息。问卷调查采用描述性统计进行总结。结果表明,不同参与者的支持体验和感知帮助程度各不相同。沟通和基于价值观的目标是大多数参与者的高度优先事项,大多数人认为文化目标很重要。研究结果强调了考虑父母和whānau声音的价值,特别是那些来自土著社区的声音。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experiences of whānau Māori caring for a young child on the autism spectrum
This mixed-methods study aimed to explore the experiences and goals of Māori parents and whānau (families) caring for young autistic children. Data were collected via a rōpū kōrero (focus group) and an online questionnaire, with a total of 33 parents and whānau participating in at least one phase of the study. Reflexive thematic analysis was used to analyse rōpū kōrero data with findings used to inform the design of an online questionnaire. Questionnaire responses were summarised using descriptive statistics. Results indicate that experience and perceived helpfulness of supports varied across participants. Communication and values-based goals were a high priority for most participants, and most rated cultural goals as important. Findings highlight the value of considering parent and whānau voices, especially those from Indigenous communities.
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来源期刊
CiteScore
2.40
自引率
10.50%
发文量
72
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