Background Electronic approaches are becoming more widely used to obtain informed
consent for research participation. Electronic consent (e-consent) provides an accessible …

Background The increasing integration of digital health tools into care may result in a greater
flow of personal health information (PHI) between patients and providers. Although privacy …

Introduction: The updated common rule, for human subjects research, requires that consents
“begin with a 'concise and focused'presentation of the key information that will most likely …

Background Newborn screening (NBS) occupies a unique space at the intersection of
translational science and public health. As the only truly population-based public health …

The concept of health literacy is increasingly being recognised as not just an individual trait,
but also as a characteristic related to families, communities, and organisations providing …

The Covid‐19 pandemic required rapid changes to research protocols, including immediate
transitions to recruiting research participants and conducting the informed consent process …

Changes in the clinical trials landscape have been driven by advancements in digital
technology. The use of electronic informed consent to inform research participants and to …

Preterm delivery remains a critical global health concern, with numerous adverse
consequences for both neonate and healthcare systems. Understanding the relationship …

Background Electronic informed consent (eIC) is increasingly used in clinical research due
to several benefits including increased enrollment and improved efficiency. Within a learning …

Background When the COVID-19 pandemic hit in 2020, researchers in the P30 Center for
the Study of Symptom Science, Metabolomics, and Multiple Chronic Conditions at Emory …