Vaccine Chatbot for Improving Influenza Vaccination Uptake

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-59
SponsorFudan University

About this trial

This study aims to assess the impact of a vaccine chatbot on improving influenza vaccination uptake among children aged between 6 and 59 months through a cluster randomized trial. Specifically, the main questions it seeks to answer are whether an AI-enabled vaccine chatbot will increase the uptake of influenza vaccine among children and their family members, and how it will influence parents' literacy and confidence towards influenza vaccine. It will explore the potential role of vaccine chatbot on vaccination services.

A cluster randomization will be used to assign children to the intervention and control groups. Parents of children in the intervention group will be invited to use the influenza vaccine chatbot online through WeChat, the mostly widely used social media platform in mainland China, or any web browsers. They can ask any questions related to the influenza vaccine and receive validated answers from the chatbot immediately. The intervention will last one and a half months, with invitations sent every ten days to reinforce the engagement. The control group will not use the chatbot during the intervention duration. After the intervention, the uptake, literacy, and confidence towards influenza vaccine will be compared between the intervention and control groups to evaluate the impact of vaccine chatbot.

Eligibility criteria

Qualifiers

Parents of the child visiting clinics.

Children aged between 6 and 59 months.

Children who have not received an influenza vaccine in both the current and previous flu seasons and have not yet made an appointment for an influenza vaccine.

Children who have no contraindications to receiving an influenza vaccine.

Disqualifiers

Children vaccinated or appointed for influenza vaccination or with any contraindication to influenza vaccine.

Parents with mental disorders or visual/reading impairments, and unable to cooperate with and undergo the intervention activities.

Unwilling to participate.

Trial design

Treatments tested in this trial

  • An AI-enabled chatbot tailored for influenza vaccine consultation

Treatment groups

1,200 Participants
are divided into 2 treatment groups

Sponsors and collaborators