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NOT YET RECRUITING
NCT07756515
NA
Chatbot Implementation In The Clinical Informed Consent Process
Sponsor: M.D. Anderson Cancer Center
View on ClinicalTrials.gov
Summary
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.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
100
Start Date
2027-01-01
Completion Date
2031-12-17
Last Updated
2026-08-10
Healthy Volunteers
No
Conditions
Interventions
OTHER
CoCo Chatbot
A patient-facing chatbot designed to obtain informed consent
Locations (1)
UT MD Anderson
Houston, Texas, United States