Department of Communication Sciences and Disorders, Fort Hays State University, KS.
Department of Communication Sciences & Disorders, Louisiana State University, Baton Rouge.
Am J Speech Lang Pathol. 2020 Nov 12;29(4):2049-2067. doi: 10.1044/2020_AJSLP-20-00049. Epub 2020 Aug 28.
Purpose This study examined caregiver perceptions of their child's language and literacy disorder as influenced by communications with their speech-language pathologist. Method The participants were 12 caregivers of 10 school-aged children with language and literacy disorders. Employing qualitative methods, a collective case study approach was utilized in which the caregiver(s) of each child represented one case. The data came from semistructured interviews, codes emerged directly from the caregivers' responses during the interviews, and multiple coding passes using ATLAS.ti software were made until themes were evident. These themes were then further validated by conducting clinical file reviews and follow-up interviews with the caregivers. Results Caregivers' comments focused on the types of information received or not received, as well as the clarity of the information. This included information regarding their child's diagnosis, the long-term consequences of their child's disorder, and the connection between language and reading. Although caregivers were adept at describing their child's difficulties and therapy goals/objectives, their comments indicated that they struggled to understand their child's disorder in a way that was meaningful to them and their child. Conclusions The findings showed the value caregivers place on receiving clear and timely diagnostic information, as well as the complexity associated with caregivers' understanding of language and literacy disorders. The findings are discussed in terms of changes that could be made in clinical practice to better support children with language and literacy disorders and their families.
本研究考察了照顾者对其子女语言和读写障碍的看法,这些看法受到与言语语言病理学家沟通的影响。
参与者为 12 名 10 岁左右有语言和读写障碍儿童的照顾者。采用定性方法,采用集体案例研究方法,每个孩子的照顾者(或多名照顾者)代表一个案例。数据来自半结构化访谈,代码直接从访谈中照顾者的回答中得出,并使用 ATLAS.ti 软件进行多次编码,直到出现主题。然后通过对照顾者的临床档案进行审查和随访访谈进一步验证这些主题。
照顾者的评论集中在收到或未收到的信息类型以及信息的清晰度上。这包括有关孩子诊断、孩子疾病的长期后果以及语言和阅读之间联系的信息。尽管照顾者能够熟练地描述孩子的困难和治疗目标/目标,但他们的评论表明,他们难以以对他们自己和孩子有意义的方式理解孩子的障碍。
研究结果表明,照顾者重视获得清晰和及时的诊断信息,以及照顾者理解语言和读写障碍的复杂性。研究结果从临床实践中可以做出哪些改变以更好地支持有语言和读写障碍的儿童及其家庭的角度进行了讨论。