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A Digital Health Application to Assess Decisional Capacity to Provide Informed Consent: Randomized Controlled Trial Protocol (Preprint)
2018
JMIR Research Protocols
Any study with human subjects must have a robust consent process to ensure that participants understand the study and can decide whether they want to be involved. Investigators must determine whether a potential study participant is able to make an informed decision and what modifications or supports are needed to maximize participation in decision making. A variety of approaches have been used to modify consent forms and the consent process to increase the research participants' decisional
doi:10.2196/10360
pmid:30455171
pmcid:PMC6277828
fatcat:c3udczvb2rdyzaaupssfyqruty