Chatbot Implementation In The Clinical Informed Consent Process

Authors
Category Primary study
Registry of TrialsClinicalTrials.gov
Year 2026
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.
Epistemonikos ID: e10c2f567087b0cbebd8e40911be542d718e971e
First added on: Aug 11, 2026