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Description

In the context of asking patients to share their health information for unspecified future research, we conducted a randomized trial comparing an interactive trust-enhanced broad e-consent to an interactive only and a standard consent. At six-month follow-up, participants who used the interactive, trust-enhanced e-consent consent reported higher satisfaction (b=0.86, p<0.0001) and understanding (b=31.94, p<0.0001). Broad e-consents may achieve better patient experiences by augmenting standard information with options to obtain more information and with trust-enhancing messages.

Learning Objective: After participating in this session, learners will be able to:

1. Identify different approaches to presenting broad e-consent electronically and their effect on decision making outcomes.
2. Discuss potential mechanisms for communicating consent information in ways that enhance patients' understanding and satisfaction with the consent process.

Authors:

Christopher Harle (Presenter)
Indiana University

Elizabeth Golembiewski, Indiana University
Kia Rahmanian, University of Florida
Babette Brumback, University of Florida
Janice Krieger, University of Florida
Kenneth Goodman, University of Miami
Arch Mainous , University of Florida
Ray Moseley, University of Florida

Presentation Materials:

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