Chatbot Implementation In The Clinical Informed Consent Process
The purpose of this study is to determine the feasibility of implementing the chatbot "CoCo" in the IC process for research studies. We hypothesize that implementing a chatbot into the IC process will facilitate accurate information delivery and enhance participant comprehension and process satisfaction compared to traditional remote consent methods.
NCI-CTRP Clinical Trials Registry
Can the SurgInfoBot Improve the Consent Process for Endoscopy? A Randomised Controlled Trial
Patient-centered Development of the Cancer Support Community's Open to Options ®Chatbot Program