Herbert Carly, Broach John, Heetderks William, Qashu Felicia, Gibson Laura, Pretz Caitlin, Woods Kelsey, Kheterpal Vik, Suvarna Thejas, Nowak Christopher, Lazar Peter, Ayturk Didem, Barton Bruce, Achenbach Chad, Murphy Robert, McManus David, Soni Apurv
Program in Digital Medicine, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA, United States.
Department of Emergency Medicine, University of Massachusetts Chan Medical School, Worcester, MA, United States.
JMIR Form Res. 2022 Oct 18;6(10):e35426. doi: 10.2196/35426.
The ongoing SARS-CoV-2 pandemic necessitates the development of accurate, rapid, and affordable diagnostics to help curb disease transmission, morbidity, and mortality. Rapid antigen tests are important tools for scaling up testing for SARS-CoV-2; however, little is known about individuals' use of rapid antigen tests at home and how to facilitate the user experience.
This study aimed to describe the feasibility and acceptability of serial self-testing with rapid antigen tests for SARS-CoV-2, including need for assistance and the reliability of self-interpretation.
A total of 206 adults in the United States with smartphones were enrolled in this single-arm feasibility study in February and March 2021. All participants were asked to self-test for COVID-19 at home using rapid antigen tests daily for 14 days and use a smartphone app for testing assistance and to report their results. The main outcomes were adherence to the testing schedule, the acceptability of testing and smartphone app experiences, and the reliability of participants versus study team's interpretation of test results. Descriptive statistics were used to report the acceptability, adherence, overall rating, and experience of using the at-home test and MyDataHelps app. The usability, acceptability, adherence, and quality of at-home testing were analyzed across different sociodemographic, age, and educational attainment groups.
Of the 206 enrolled participants, 189 (91.7%) and 159 (77.2%) completed testing and follow-up surveys, respectively. In total, 51.3% (97/189) of study participants were women, the average age was 40.7 years, 34.4% (65/189) were non-White, and 82% (155/189) had a bachelor's degree or higher. Most (n=133/206, 64.6%) participants showed high testing adherence, meaning they completed over 75% of the assigned tests. Participants' interpretations of test results demonstrated high agreement (2106/2130, 98.9%) with the study verified results, with a κ score of 0.29 (P<.001). Participants reported high satisfaction with self-testing and the smartphone app, with 98.7% (157/159) reporting that they would recommend the self-test and smartphone app to others. These results were consistent across age, race/ethnicity, and gender.
Participants' high adherence to the recommended testing schedule, significant reliability between participants and study staff's test interpretation, and the acceptability of the smartphone app and self-test indicate that self-tests for SARS-CoV-2 with a smartphone app for assistance and reporting is a highly feasible testing modality among a diverse population of adults in the United States.
正在肆虐的新型冠状病毒肺炎(SARS-CoV-2)疫情使得开发准确、快速且经济实惠的诊断方法成为必要,以帮助遏制疾病传播、发病率和死亡率。快速抗原检测是扩大SARS-CoV-2检测规模的重要工具;然而,对于个人在家中使用快速抗原检测的情况以及如何提升用户体验,我们知之甚少。
本研究旨在描述使用快速抗原检测进行SARS-CoV-2系列自我检测的可行性和可接受性,包括对协助的需求以及自我解读的可靠性。
2021年2月和3月,共有206名在美国拥有智能手机的成年人参与了这项单臂可行性研究。所有参与者被要求在家中每天使用快速抗原检测进行14天的新冠病毒自我检测,并使用一款智能手机应用程序获取检测协助并报告结果。主要结果包括对检测计划的依从性、检测及智能手机应用程序体验的可接受性,以及参与者与研究团队对检测结果解读的可靠性。描述性统计用于报告在家检测和MyDataHelps应用程序的可接受性、依从性、总体评分及使用体验。对不同社会人口统计学、年龄和教育程度组别的家庭检测的可用性、可接受性、依从性和质量进行了分析。
在206名登记参与者中,分别有189名(91.7%)和159名(77.2%)完成了检测和随访调查。总体而言,51.3%(97/189)的研究参与者为女性,平均年龄为40.7岁,34.4%(65/189)为非白人,82%(155/189)拥有学士学位或更高学历。大多数(n = 133/206,64.6%)参与者表现出较高的检测依从性,即他们完成了超过75%的指定检测。参与者对检测结果的解读与研究核实结果高度一致(2106/2130,98.9%),κ值为0.29(P <.001)。参与者对自我检测和智能手机应用程序满意度较高,98.7%(157/159)的参与者表示会向他人推荐自我检测和智能手机应用程序。这些结果在年龄、种族/族裔和性别方面是一致的。
参与者对推荐检测计划的高度依从性、参与者与研究人员对检测结果解读之间的显著可靠性,以及智能手机应用程序和自我检测的可接受性表明,在美国不同成年人群体中,借助智能手机应用程序进行协助和报告的SARS-CoV-2自我检测是一种高度可行的检测方式。