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Interested participants were asked to complete a consent form using an e-consent process. At a convenient time for the participant, the research coordinator trained in collecting informed consent, called the participant on the phone to review the full consent form. The consent form listed the study procedures and risks and benefits involved with the study. Participants were reminded that their participation was voluntary and that they could ask to withdraw at any time.
JMIR Form Res 2025;9:e60495
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The e SCCIP/e SCCIP-SP and education control programs have been built in the most recent version of the Research Infrastructure Containing e-interventions system developed and maintained by the University of Virginia Center for Behavioral Health and Technology. This platform provides the tools to both deliver robust digital health interventions as well as to manage participants in research trials.
JMIR Res Protoc 2023;12:e46339
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