{"title":"Parental Issues and Support Needs in Selective Mutism in Japan: A Quantitative Content Analysis.","authors":"Tomohisa Yamanaka, Honami Koyama, Masahiko Inoue","doi":"10.33160/yam.2024.11.004","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":23795,"journal":{"name":"Yonago acta medica","volume":"67 4","pages":"303-313"},"PeriodicalIF":0.9000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11584234/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Yonago acta medica","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.33160/yam.2024.11.004","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: 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.
Methods: 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.
Results: 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.
Conclusion: 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.
背景:选择性缄默症(SM)是一种焦虑症,患儿在特定的社交场合难以开口说话,家长往往难以应对患儿的症状。我们通过家长对两个开放式问题的回答,分析了他们在选择性缄默症方面的问题和支持需求,研究了这些需求在诊断和并发症方面的差异:我们对通过 SM 信息交流群和社交网络服务招募的 70 名 SM 患儿家长(29-63 岁)的回答进行了定量内容分析。参与者回答了两个开放式问题,内容涉及他们所面临的问题以及他们在子女出现 SM 症状时所需要的支持:结果显示,有 SM 症状的儿童的家长所面临的问题可分为五类:(A)对延迟最初反应感到后悔;(B)有 SM 症状的儿童缺课;(C)教师的支持不足;(D)与他人沟通不周到,缺乏同理心;以及(E)沟通障碍导致欺凌和社会孤立。家长的支持需求分为四类:(a)咨询和获取信息的场所;(b)了解 SM 的支持者人数的增长;(c)增进 SM 知识的机会;以及(d)改善 SM 的具体方法。此外,虽然合并症对家长的问题和支持需求没有显著影响,但根据诊断结果,家长的需求和支持需求略有不同:本研究强调,患有 SM 的儿童的家长对专业人员缺乏了解和他们孩子的症状感到困扰,这促使他们寻求更好的理解和更多的资源。研究结果还表明,这些家长的支持需求因其子女是否被诊断为 SM 而异。未来的研究应从全球范围内找出家长的问题和支持需求,确定核心要素,并建立一个更全面的支持系统。
期刊介绍:
Yonago Acta Medica (YAM) is an electronic journal specializing in medical sciences, published by Tottori University Medical Press, 86 Nishi-cho, Yonago 683-8503, Japan.
The subject areas cover the following: molecular/cell biology; biochemistry; basic medicine; clinical medicine; veterinary medicine; clinical nutrition and food sciences; medical engineering; nursing sciences; laboratory medicine; clinical psychology; medical education.
Basically, contributors are limited to members of Tottori University and Tottori University Hospital. Researchers outside the above-mentioned university community may also submit papers on the recommendation of a professor, an associate professor, or a junior associate professor at this university community.
Articles are classified into four categories: review articles, original articles, patient reports, and short communications.