Chatbot Implementation In The Clinical Informed Consent Process (NCT07756515)
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: UT MD Anderson — Houston, Texas
Age range: 18 Years
🧪 Interventions in This Study
- CoCo Chatbot (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- UT MD Anderson — Houston, Texas
📞 Contact the Study Coordinator
Phone: (713) 794-1226
Email: fmeric@mdanderson.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Informed Consent
- Digital-Supported Versus Standard Consent for Advanced Therapeutic Endoscopy — Toronto, Ontario
- AI-Driven Consent Simplification Study — Los Angeles, California
Explore by condition: All Informed Consent clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.