Exploring knowledge and attitudes toward electronic informed consent among clinical trial participants in China: a cross-sectional study.

IF 3.1 1区 哲学 Q1 ETHICS
Ying Wu, Xing Liu, Xiaoying Ge, Xin Tan, Weiwei Yu, Xiaomin Wang
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引用次数: 0

Abstract

Background: With the extensive integration of digital technology into clinical research, intelligence, virtualization, and decentralization have gradually transformed into emerging clinical research modes, the electronization of informed consent has become indispensable to the development of clinical trial informatization, and the inclination to use electronic informed consent (eIC) has grown. The knowledge and perceptions of research participants, as objects of informed consent acquisition, regarding eIC are crucial. However, few studies have empirically explored such issues.

Methods: This cross-sectional study was conducted at three general hospitals in south-central China from July to September 2022. An online survey questionnaire was adapted and administered via WeChat to investigate the issues of interest.

Results: A total of 388 valid questionnaires were included in the analysis. The results showed that the overall response rate for the knowledge section of the questionnaire exceeded 70%. Of the respondents, 53.1% had heard of the term "electronic informed consent," but only 43.2% had used eIC. The majority of respondents (68%) expressed a preference for using eIC and demonstrated a positive attitude toward it. However, some participants expressed concerns regarding the security and confidentiality (64.4%), operational complexity (52.3%), and effectiveness of online interaction (59.3%) in eIC. Statistically significant relationships were observed between participants' attitude scores and their age, gender, type of participation, and frequency of involvement in clinical research. Additionally, a positive and statistically significant correlation was found between participants' knowledge scores and their attitude scores.

Conclusion: The results of this study indicate that most participants have a good understanding of eIC-related knowledge and hold a positive attitude toward its implementation. However, they also express concerns about data protection and privacy security in eIC. These findings provide a foundation for developing targeted strategies to enhance the adoption and acceptance of eIC among diverse populations.

探讨中国临床试验参与者对电子知情同意的知识和态度:一项横断面研究。
背景:随着数字技术在临床研究中的广泛融合,智能化、虚拟化、去中心化逐渐转变为新兴的临床研究模式,知情同意电子化成为临床试验信息化发展不可或缺的一部分,使用电子知情同意(electronic informed consent, eIC)的倾向日益增强。作为获得知情同意的对象,研究参与者关于eIC的知识和看法至关重要。然而,很少有研究对这些问题进行实证探讨。方法:横断面研究于2022年7 - 9月在中国中南部三家综合医院进行。通过微信调整和管理了一份在线调查问卷,以调查感兴趣的问题。结果:共回收有效问卷388份。结果显示,问卷知识部分的总体答复率超过70%。受访者中,53.1%曾听说“电子知情同意书”一词,但只有43.2%曾使用电子知情同意书。大多数受访者(68%)表示倾向于使用eIC,并表现出积极的态度。然而,一些与会者对电子商务中的安全性和保密性(64.4%)、操作复杂性(52.3%)和在线互动的有效性(59.3%)表示担忧。被试的态度得分与其年龄、性别、参与类型、参与临床研究的频率之间存在显著的统计学关系。此外,被试的知识得分与态度得分之间存在显著的正相关。结论:本研究结果显示,大部分被试对电子商务相关知识有较好的了解,并对实施电子商务持积极态度。然而,他们也对电子商务中的数据保护和隐私安全表示担忧。这些发现为制定有针对性的策略提供了基础,以提高不同人群对eIC的采用和接受程度。
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来源期刊
BMC Medical Ethics
BMC Medical Ethics MEDICAL ETHICS-
CiteScore
5.20
自引率
7.40%
发文量
108
审稿时长
>12 weeks
期刊介绍: BMC Medical Ethics is an open access journal publishing original peer-reviewed research articles in relation to the ethical aspects of biomedical research and clinical practice, including professional choices and conduct, medical technologies, healthcare systems and health policies.
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