Yamanaka Tomohisa, Koyama Honami, Inoue Masahiko
Department of Doctoral Course, Graduate School of Medical Sciences, Tottori University, Yonago 683-8503, Japan.
Student Accessibility Office, Head Office for Education and Student Support, Shimane University, Matsue 690-8504, Japan.
Yonago Acta Med. 2024 Nov 1;67(4):303-313. doi: 10.33160/yam.2024.11.004. eCollection 2024 Nov.
Selective mutism (SM) is an anxiety disorder in which children struggle to speak in specific social situations, and parents often have trouble coping with their child's symptoms. We analyzed parents' issues and support needs regarding SM through their responses to two open-ended questions, examining how these needs varied with diagnosis and comorbid conditions.
Quantitative content analysis was conducted on responses obtained from 70 parents of children with SM (ages 29-63 years) recruited through SM information exchange group and social networking service. The participants responded to two open-ended questions regarding the issues they faced and the support they needed for their children's SM symptoms.
The results showed that issues faced by parents of children with SM could be divided into five groups: (A) Regret over Delayed Initial Response, (B) School Non-attendance in Children with SM, (C) Inadequate Support from Teachers, (D) Inconsiderate Communication Lacking Empathy from Others, and (E) Communication Barriers Leading to Bullying and Social Isolation. The support needs of parents were categorized into four groups: (a) Places for Consultation and Obtaining Information, (b) Growth in the Number of Supporters Who Understand SM, (c) Opportunities to Improve Knowledge about SM, and (d) Specific Methods for SM Improvement. Furthermore, although comorbid conditions did not significantly affect parental issues and support needs, slight differences were observed based on the presence of a diagnosis.
This study highlights that parents of children with SM are troubled by professionals' lack of knowledge and their children's symptoms, driving them to seek better understanding and more resources. The results also suggest that the support needs of these parents vary depending on whether their child is diagnosed with SM. Future research should globally identify parental issues and support needs, determine the core elements, and establish a more comprehensive support system.
选择性缄默症(SM)是一种焦虑症,患病儿童在特定社交场合难以开口说话,家长往往难以应对孩子的症状。我们通过分析家长对两个开放式问题的回答,探讨了他们在选择性缄默症方面的问题和支持需求,研究这些需求如何因诊断结果和共病情况而有所不同。
对通过选择性缄默症信息交流小组和社交网络服务招募的70名选择性缄默症患儿家长(年龄在29 - 63岁之间)的回答进行了定量内容分析。参与者回答了两个关于他们面临的问题以及孩子选择性缄默症症状所需支持的开放式问题。
结果表明,选择性缄默症患儿家长面临的问题可分为五组:(A)对初期反应延迟的遗憾,(B)选择性缄默症患儿的缺课情况,(C)教师支持不足,(D)他人缺乏同理心的不当沟通,以及(E)导致欺凌和社交孤立的沟通障碍。家长的支持需求分为四组:(a)咨询和获取信息的场所,(b)了解选择性缄默症的支持者数量增加,(c)提高对选择性缄默症认识水平的机会,以及(d)改善选择性缄默症的具体方法。此外,虽然共病情况对家长的问题和支持需求没有显著影响,但根据诊断结果的有无观察到了细微差异。
本研究强调,选择性缄默症患儿的家长因专业人员知识匮乏和孩子的症状而困扰,促使他们寻求更好的理解和更多资源。结果还表明,这些家长的支持需求因孩子是否被诊断为选择性缄默症而有所不同。未来的研究应全面识别家长的问题和支持需求,确定核心要素,并建立更全面的支持系统。