Actively Recruiting
Effectiveness of Vaccine Chatbot on HPV Vaccine Awareness and Vaccination in China
Led by Fudan University · Updated on 2024-06-12
1800
Participants Needed
2
Research Sites
27 weeks
Total Duration
On this page
Sponsors
F
Fudan University
Lead Sponsor
T
The University of Hong Kong
Collaborating Sponsor
AI-Summary
What this Trial Is About
This interventional study targets female students in junior middle school. It goal is to evaluate the effectiveness of a vaccine chatbot on HPV vaccine awareness and vaccination. The main questions it aims to answer are: 1. How will the novel digital tool, a vaccine chatbot, impact eligible parents' awareness and knowledge of HPV vaccines, their willingness to vaccinate their daughters, and vaccination status of female students. 2. How is the vaccine chatbots accepted by all stakeholders, and what are the facilitators of and barriers to implementing vaccine chatbot promotion campaign. The intervention group will go through the intervention measure while the control group will not: 1. The intervention group will be invited to use the HPV 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 HPV vaccine and get validated answers from the chatbot immediately. The intervention lasts two weeks, with invitations sent every four days to reinforce the intervention. 2. The control group will not use the chatbot during the intervention duration. Researchers will compare participants' HPV vaccine awareness, and vaccination intention and status after intervention between intervention group and control group to evaluate if the vaccine chatbot improves HPV vaccine awareness and vaccination.
CONDITIONS
Official Title
Effectiveness of Vaccine Chatbot on HPV Vaccine Awareness and Vaccination in China
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Parents of female students in middle school
- Female students not vaccinated or scheduled for HPV vaccination and without contraindications
- Participants without mental disorders or visual/reading impairments and able to cooperate with study activities
- Participants who have given informed consent and are willing to participate
You will not qualify if you...
- Students already vaccinated or scheduled for HPV vaccination or with contraindications to HPV vaccines
- Participants with mental disorders or visual/reading impairments unable to cooperate with study activities
- Participants unwilling to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Chizhou Health Center for Disease Control and Prevention
Chizhou, Anhui, China, 247100
Actively Recruiting
2
Jiading District Center for Disease Control and Prevention
Shanghai, Shanghai Municipality, China
Actively Recruiting
Research Team
Z
Zhiyuan Hou, PhD
CONTACT
L
Leesa Lin, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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