基于网络的帕金森病遗传学教育工具的用户和可用性测试:混合方法研究

Noah Han, Rachel A Paul, Tanya Bardakjian, Daniel Kargilis, Angela R Bradbury, Alice Chen-Plotkin, Thomas F Tropea
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引用次数: 0

摘要

基因检测对于确定临床试验的研究参与者至关重要,这些临床试验招募了携带葡萄糖脑苷酶(GBA)或富亮氨酸重复激酶2 (LRRK2)基因变异的帕金森病(PD)患者。在神经遗传学或遗传咨询方面受过训练的专业人员有限是增加检测的主要障碍。远程医疗解决方案可以增加获得遗传学教育的机会,有助于解决咨询师可用性的问题,并为患者和家庭成员提供选择。作为测试前遗传咨询的替代方案,我们开发了一个基于网络的遗传教育工具,专注于帕金森病的GBA和LRRK2测试,称为交互式多媒体方法遗传咨询,以告知和教育帕金森病(imagination -PD),并进行了用户测试和可用性测试。目标是进行用户和可用性测试,以获得涉众的反馈,以改进IMAGINE-PD。遗传咨询师、PD和神经遗传学主题专家为IMAGINE-PD开发了专门关注GBA和LRRK2基因检测的内容。根据美国卫生和人类服务部基于研究的网页设计和可用性指南,对11名运动障碍专家和13名PD患者进行了结构化访谈,以评估IMAGINE-PD在用户测试中的内容,并对12名PD患者进行了高保真原型的可用性评估。定性数据分析告知变更,以创建最终版本的IMAGINE-PD。定性资料由3名评价员进行审查。从运动障碍专家和PD患者在用户测试中的反馈数据中确定主题,包括3个方面:内容(如所涵盖的主题),功能(如网站导航)和外观(如图片和颜色)。同样,对可用性测试反馈的定性分析确定了这3个领域的其他主题。反馈的关键点是由审稿人考虑到评论的重要性和类似评论的频率一致确定的。根据每个主题的评估人员在用户测试和可用性测试阶段的一致建议,对IMAGINE-PD进行了改进,以创建IMAGINE-PD的最终版本。内容审查和可用性测试的用户测试通知了IMAGINE-PD的改进,以开发这一专注于GBA和LRRK2测试的遗传教育工具。这种利益相关者知情干预与标准远程遗传咨询方法的比较正在进行中。
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User and Usability Testing of a Web-Based Genetics Education Tool for Parkinson Disease: Mixed Methods Study.

Background: Genetic testing is essential to identify research participants for clinical trials enrolling people with Parkinson disease (PD) carrying a variant in the glucocerebrosidase (GBA) or leucine-rich repeat kinase 2 (LRRK2) genes. The limited availability of professionals trained in neurogenetics or genetic counseling is a major barrier to increased testing. Telehealth solutions to increase access to genetics education can help address issues around counselor availability and offer options to patients and family members.

Objective: As an alternative to pretest genetic counseling, we developed a web-based genetics education tool focused on GBA and LRRK2 testing for PD called the Interactive Multimedia Approach to Genetic Counseling to Inform and Educate in Parkinson's Disease (IMAGINE-PD) and conducted user testing and usability testing. The objective was to conduct user and usability testing to obtain stakeholder feedback to improve IMAGINE-PD.

Methods: Genetic counselors and PD and neurogenetics subject matter experts developed content for IMAGINE-PD specifically focused on GBA and LRRK2 genetic testing. Structured interviews were conducted with 11 movement disorder specialists and 13 patients with PD to evaluate the content of IMAGINE-PD in user testing and with 12 patients with PD to evaluate the usability of a high-fidelity prototype according to the US Department of Health and Human Services Research-Based Web Design & Usability Guidelines. Qualitative data analysis informed changes to create a final version of IMAGINE-PD.

Results: Qualitative data were reviewed by 3 evaluators. Themes were identified from feedback data of movement disorder specialists and patients with PD in user testing in 3 areas: content such as the topics covered, function such as website navigation, and appearance such as pictures and colors. Similarly, qualitative analysis of usability testing feedback identified additional themes in these 3 areas. Key points of feedback were determined by consensus among reviewers considering the importance of the comment and the frequency of similar comments. Refinements were made to IMAGINE-PD based on consensus recommendations by evaluators within each theme at both user testing and usability testing phases to create a final version of IMAGINE-PD.

Conclusions: User testing for content review and usability testing have informed refinements to IMAGINE-PD to develop this focused, genetics education tool for GBA and LRRK2 testing. Comparison of this stakeholder-informed intervention to standard telegenetic counseling approaches is ongoing.

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