Understanding the experience of users of communication aids and applications through focus group discussions with people with aphasia and family members

IF 1.5 Q2 COMMUNICATION
N. Azevedo, G. Le Dorze, G. Jarema, Christine Alary Gauvreau, Tatiana Ogourtsova, Stéfanie Beaulieu, Christel Beaujard, Marc Yvon, E. Kehayia
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引用次数: 0

Abstract

The present study sought to identify the communication needs of persons with aphasia (PWA) and of their spouses, that could ultimately be addressed with current communication aids or applications (CA/A). Among users of CA/A we solicited their opinions and experiences with current CA/A. In contrast, among those not using CA/A, we explored why they did not use CA/A. A qualitative experiential research design was used through two in-person focus groups, one in English and one in French, at a large rehabilitation hospital in the Greater Montréal region (Canada). Participants' responses were recorded, transcribed and analyzed. The thematic analysis that ensued allowed the identification of four main themes. The first theme reflects participants' observations and experiences when communicating with aphasia. The second theme regrouped responses related to successful communication with the help of CA/A. The participants' challenges and dissatisfaction with CA/A were grouped into the third theme. Lastly, a fourth theme included participants' general views about CA/A and their wishes for further development. Participants' experience with communication difficulties following aphasia and the barriers and potential facilitators to adoption of CA/A were brought to the forefront. They also highlighted those features necessary to ensuring functional uptake of CA/A by those who would benefit from it. Finally, the importance of providing training to the communication partner and sensitizing the public to the impact of aphasia on people's daily lives and on the potential benefits of using CA/A were raised as necessary future actions.
通过与失语症患者及其家人进行焦点小组讨论,了解交流辅助工具和应用程序用户的使用体验
本研究旨在确定失语症患者(PWA)及其配偶的交流需求,这些需求最终可以通过现有的交流辅助工具或应用程序(CA/A)来解决。在 CA/A 的使用者中,我们征求了他们对当前 CA/A 的意见和经验。相反,对于那些不使用 CA/A 的人,我们则探讨了他们不使用 CA/A 的原因。我们采用了定性体验式研究设计,在大蒙特利尔地区(加拿大)的一家大型康复医院,通过两个面对面的焦点小组,一个用英语,一个用法语。对参与者的回答进行了记录、转录和分析。随后进行的专题分析确定了四个主要专题。第一个主题反映了参与者在与失语者交流时的观察和经验。第二个主题重新组合了与借助 CA/A 成功交流有关的回答。参与者对 CA/A 的挑战和不满被归入第三个主题。最后,第四个主题包括参与者对 CA/A 的总体看法以及对进一步发展的愿望。与会者对失语症后交流困难的经历,以及采用 CA/A 的障碍和潜在的促进因素,都被放在了最重要的位置。他们还强调了那些必要的特征,以确保那些将从中受益的人在功能上接受 CA/A。最后,与会者提出了为交流伙伴提供培训的重要性,以及向公众宣传失语症对人们日常生活的影响和使用 CA/A 的潜在益处的重要性,认为这是今后必须采取的行动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.30
自引率
8.30%
发文量
284
审稿时长
14 weeks
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