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Evaluation of a Vaccine Chatbot on HPV Vaccine Confidence and Hesitancy
Evaluation of a Vaccine Chatbot on HPV Vaccine Confidence and Hesitancy

NCT07200570

Not Yet RecruitingNA

Sponsor: Fudan University

Conditions: HPV Vaccine

Interventions: LLM-Powered HPV Vaccine Chatbot

The goal of this clinical trial is to learn if a chatbot powered by artificial intelligence works to improve HPV vaccination among females aged 15 to 45 in China. A randomized controlled trial and implementation science study will be conducted targeting females as participants. The main questions it aims to answer are: 1. Does the vaccine chatbot influence women's confidence, literacy, hesitancy, and uptake of the HPV vaccine. 2. What are the public acceptance of chatbot and the facilitators and barriers to its implementation in a real-world setting. Researchers will compare a group of women who use the chatbot with a group who do not use it to see if the chatbot is effective at helping women feel confident and willing to get vaccinated against HPV. Participants will: 1. Be recruited and randomly allocated into one of two groups. One group will be invited to use the HPV vaccine chatbot and the other group will not get access to the vaccine chatbot until the end of the trial. 2. Complete a questionnaire survey on their confidence, literacy, and hesitancy on the HPV vaccine. 3. Have their vaccination status checked at the end of trial.

Eligibility overview

Sex: FEMALE

Age: 15 Years to 45 Years

Healthy volunteers: Yes

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Female, aged 15 to 45 years, inclusive.
* Not previously vaccinated against HPV.
* Reports no contraindications to HPV vaccination.
* Has no mental, visual, or reading impairments that would preclude cooperation with study activities.
* Is willing and able to provide informed consent.

Exclusion Criteria:

* Male.
* Age under 15 or over 45 years.
* Has a history of prior HPV vaccination.
* Has a known contraindication to HPV vaccination.
* Unable to comply with study procedures.
* Is unwilling or unable to provide informed consent.