Actively Recruiting

Phase Not Applicable
Age: 14Years +
All Genders
Healthy Volunteers
ID05789901

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

Led by McGill University Health Centre/Research Institute of the McGill University Health Centre · Updated on 2024-03-06

400

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

Sponsors

M

McGill University Health Centre/Research Institute of the McGill University Health Centre

Lead Sponsor

C

Centre hospitalier de l'Université de Montréal (CHUM)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a master research protocol to adapt and evaluate the MARVIN chatbot, an artificial intelligence-based conversational agent, for providing information across different health conditions such as HIV infections, breast cancer, and pediatric infectious conditions. This study uses an adaptive platform trial design to allow multiple chatbot interventions tailored to various populations, enabling early withdrawal of ineffective arms and introduction of new ones. The goal is to develop, adapt, and assess the usability and implementation outcomes of these chatbots through co-construction with participants and research teams. The study involves four chatbot interventions delivered via Meta (Facebook) Messenger: MARVIN for HIV patients, MARVIN-Pharma for community pharmacists, MARVINA for breast cancer patients, and MARVIN-CHAMP for pediatric patients with infectious conditions. Participants will be involved in co-constructing the chatbots, usability studies, implementation, evaluation of outcomes, and continuous improvements. This ongoing process allows the chatbots to be progressively refined to meet the needs of each user group. Participants aged 14 and older who understand the study requirements and have access to a smartphone, tablet, or computer with internet or data plan will engage with the chatbots over time. Researchers will assess usability using tools like the Usability Metric for User eXperience (UMUX-Lite) and Acceptability E-Scale (AES) immediately and at intervals over 12 months. They will also evaluate implementation outcomes such as intervention appropriateness and compatibility. Throughout the study, participants' interaction with the chatbots and their experience will be continuously monitored and improved.

CONDITIONS

Brief Title

The MARVIN Chatbots to Provide Information for Different Health Conditions

Who Can Participate

Age: 14Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 14 years of age or older
  • Fluent in English and/or French
  • Able to understand study requirements and provide informed consent
  • Have access to a smartphone, tablet, or computer at home or workplace
  • Have internet access or a data plan on their device
  • Willing to use a Facebook Messenger-based chatbot
  • Agree to use or create a personal Facebook account
  • Accept Facebook's privacy and data security policies
Not Eligible

You will not qualify if you...

  • Not meeting all inclusion criteria
  • Any condition judged by the investigator that makes participation inappropriate, such as cognitive deficits

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) to confirm eligibility and provide informed consent

Co-construction and Usability Testing

Duration - 1 month

Participants collaborate in adapting the chatbot and evaluate its usability in their specific healthcare context.

Initial baseline visit followed by usage over 1 month with remote check-ins

Implementation and Outcome Evaluation

Duration - Up to 12 months

Participants use the chatbot over time while researchers evaluate implementation fidelity and user outcomes such as acceptability and appropriateness.

Quarterly visits (every 3 months) for assessments over 12 months

Trial Site Locations

Total: 2 locations

1

Centre hospitalier de l'Université de Montréal (CHUM)

Montreal, Quebec, Canada, H2X 3E4

Actively Recruiting

2

McGill University Health Centre (MUHC)

Montreal, Quebec, Canada, H4A 3J1

Actively Recruiting

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Research Team

B

Bertrand Lebouché, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

4

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Published Research Related To This Trial

Adapting and Evaluating an AI-Based Chatbot Through Patient and Stakeholder Engagement to Provide Information for Different Health Conditions: Master Protocol for an Adaptive Platform Trial (the MARVIN Chatbots Study).

Yuanchao Ma, Sofiane Achiche, Marie-Pascale Pomey...

https://pubmed.ncbi.nlm.nih.gov/38349734