🏛️ Verified NIH Record • Updated 2024-03-04

The MARVIN Chatbots to Provide Information for Different Health Conditions (NCT05789901)

A Master Research Protocol to Adapt and Evaluate an Artificial Intelligence Based Conversational Agent to Provide Information for Different Health Conditions: the MARVIN Chatbots

🟢 Recruiting Observational / Diagnostic 📋 Clinical Research Protocol Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre

🩺 Plain-English Summary (8th-Grade Level)

This research is a continuation of a usability study with the MARVIN chatbot. The investigators aim to adapt the MARVIN chatbot to open it to other health domains (e.g. breast cancer) and populations (e.g. pharmacists). Therefore, this protocol constitutes a master research protocol that will englobe different research projects with individual chatbots. The investigators adopt an adaptive platform trial design, which will allow flexibility in handling multiple interventions adapted to different populations while retaining the characteristics of a platform trial design allowing early withdrawal of ineffective trial arms based on interim data (implementation outcomes) and introduction of new trial arms.

Who can join: Review the eligibility criteria below.

Location: Centre hospitalier de l'Université de Montréal (CHUM) — Montreal, Quebec

Age range: 14 Years

🧪 Interventions in This Study

  • MARVIN (OTHER)
  • MARVIN-Pharma (OTHER)
  • MARVINA (OTHER)
  • MARVIN-CHAMP (OTHER)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (2 Sites)

  • Centre hospitalier de l'Université de Montréal (CHUM) — Montreal, Quebec
  • McGill University Health Centre (MUHC) — Montreal, Quebec

📞 Contact the Study Coordinator

Phone: (514) 843-2090

Email: bertrand.lebouche@mcgill.ca

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.

Explore by condition: All HIV Infections clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗