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• W2508346741 abstract "ABSTRACTHuman subjects research generally requires the informed consent of participants. Investigators often conduct the informed consent process using printed documents and physical signatures, which can be logistically complex in large-scale educational studies. Although the medical community has begun routinely using electronic consent systems as part of the international movement from paper-based to electronic health records, educational researchers have been slower to adopt this approach due, perhaps, to concerns about the legality of collecting consent online. This article clarifies the issue for educational researchers and, by extension, others engaged in human subjects research, by discussing whether conducting the informed consent process online complies with the US Federal Policy for the Protection of Human Subjects [US Department of Health and Human Services, n.d.-b, Code of federal regulations (45 CFR 46). Retrieved from http://www.hhs.gov/ohrp/humansubjects/guidance/45cfr46.html] as well as t..." @default.
• W2508346741 created "2016-09-16" @default.
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• W2508346741 date "2015-01-02" @default.
• W2508346741 modified "2023-09-23" @default.
• W2508346741 title "Implementing electronic informed consent in educational research: benefits and barriers†" @default.
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• W2508346741 doi "https://doi.org/10.1080/18340806.2015.1222645" @default.
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