This article reviews the peer-reviewed literature addressing the healthcare information
available on YouTube. Inclusion and exclusion criteria were determined, and the online …

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

Although experts have identified benefits to replacing paper with electronic consent
(eConsent) for research, a comprehensive understanding of strategies to overcome barriers …

Background: Telemedicine systems are gaining attention nationwide as a means for
providing care in remote areas and allowing a small number of providers to impact a large …

Lack of recruitment of qualified research participants continues to be a significant bottleneck
in clinical trials, often resulting in costly time extensions, underpowered results, and in some …

Objective Digital technologies create opportunities for improvement of consenting processes
in clinical care. Yet little is known about the prevalence, characteristics or outcomes of …

Purpose Ethical and legal requirements for healthcare providers in the United States,
stipulate that patients sign a consent form prior to undergoing medical treatment or …

Background: Implementation of patient preferences for use of electronic health records for
research has been traditionally limited to identifiable data. Tiered e-consent for use of de …

Background The COVID-19 pandemic has posed daunting challenges when conducting
clinical research. Adopting new technologies such as remote electronic consent (e-Consent) …

Electronic health records (EHRs) provide great promise for identifying cohorts and
enhancing research recruitment. Such approaches are sorely needed, but there are few …