Using a chat-based informed consent tool in large-scale genomic research.

Savage, Sarah K; LoTempio, Jonathan; Smith, Erica D; Andrew, E Hallie; Mas, Gloria; Kahn-Kirby, Amanda H; Délot, Emmanuèle; Cohen, Andrea J et al. · J Am Med Inform Assoc · 2024

prospective_cohort · Level II

Where this comes from

Abstract

We implemented a chatbot consent tool to shift the time burden from study staff in support of a national genomics research study. We created an Institutional Review Board-approved script for automated chat-based consent. We compared data from prospective participants who used the tool or had traditional consent conversations with study staff. Chat-based consent, completed on a user's schedule, was shorter than the traditional conversation. This did not lead to a significant change in affirmative consents. Within affirmative consents and declines, more prospective participants completed the chat-based process. A quiz to assess chat-based consent user understanding had a high pass rate with no reported negative experiences. Our report shows that a structured script can convey important information while realizing the benefits of automation and burden shifting. Analysis suggests that it may be advantageous to use chatbots to scale this rate-limiting step in large research projects.

Medical subject headings