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Article

Assessment of the understanding of informed consent including participants’ experiences, and generation of a supplemental consent decision aid for Gestational Diabetes Mellitus (GDM) research

2018-03-29

Abstract excerpt

<h4>Background: </h4> Informed consent is a basic ethical requirement of clinical research, yet deficiencies have been documented in the comprehension of its components among trial participants. Pregnancy research is sparsely conducted. Assessment of understanding of the informed consent among pregnant women suffering from Gestational Diabetes Mellitus enrolled in a randomized controlled trial, and their experienc...

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Literature Corpus work
964c13df-700e-5dc3-a06e-d39a3f90e135
DOI
10.12688/hrbopenres.12811.1
Open publication

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Assessment of the understanding of informed consent including participants’ experiences, and generation of a supplemental consent decision aid for Gestational Diabetes Mellitus (GDM) researchDOI 10.12688/hrbopenres.12811.1
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