A Chatbot Intervention for Reducing HPV Vaccine Hesitancy
1 other identifier
interventional
456
1 country
1
Brief Summary
The goal of this project is to test the efficacy of a chatbot intervention for reducing HPV vaccine hesitancy among African American parents. An online experiment will be conducted to test the effectiveness of the chatbot intervention with African American parents. Results of this project will inform future communication interventions for reducing vaccine hesitancy among African American parents.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 6, 2023
CompletedFirst Posted
Study publicly available on registry
July 25, 2023
CompletedStudy Start
First participant enrolled
July 26, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 8, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 8, 2023
CompletedResults Posted
Study results publicly available
October 21, 2024
CompletedOctober 21, 2024
July 1, 2024
13 days
July 6, 2023
July 23, 2024
July 23, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
Attitudes Toward HPV Vaccination
Participants' attitudes toward HPV vaccination were measured by seven questions such as "The HPV vaccine is beneficial for adolescents." The responses were recorded on 1 (strongly disagree) to 5 (strongly agree) scales. Final score was the average of all 7 questions.
baseline posttest (test took approximately 5 minutes to complete)
Intentions Toward HPV Vaccination
Participants' intentions toward vaccinating their children against HPV were measured by three questions such as "I am likely to get my child/children the HPV vaccine." Responses were indicated on 1 (strongly disagree) to 5 (strongly agree) scales. The final score was the average of the three questions.
baseline posttest (test took approximately 5 minutes to complete)
Secondary Outcomes (1)
Ratings of the Chatbot
baseline posttest (test took approximately 5 minutes to complete)
Study Arms (3)
Personalized Chatbot Condition
EXPERIMENTALAfter reading a standard CDC HPV vaccine message, participants will interact with a chatbot designed to deliver personalized HPV vaccine messages (i.e., tailored to their personalities).
Non-Personalized Chatbot Condition
EXPERIMENTALAfter reading a standard CDC HPV vaccine message, participants will interact with a chatbot designed to deliver HPV vaccine messages, which are not tailored to their personalities.
No Chatbot Control Condition
ACTIVE COMPARATORParticipants will read a standard CDC HPV vaccine message without interacting with any chatbot that delivers additional messages.
Interventions
In this intervention, participants will first see a standard CDC HPV vaccine message. After that they will be invited to interact with a chatbot designed to deliver additional HPV vaccine messages, which are tailored to their personalities.
In this intervention, participants will first see a standard CDC HPV vaccine message. After that they will be invited to interact with a chatbot designed to deliver additional HPV vaccine messages, which are not tailored to their personalities.
In this intervention, participants will see a standard CDC HPV vaccine message only and will not interact with any chatbot.
Eligibility Criteria
You may qualify if:
- years or older
- Self-identify as Black or African American
- Parents of children under 18 years old
- Access to computer/laptop/mobile device and the Internet
You may not qualify if:
- Under 18 years
- Does not self-identify as Black or African American
- Not a parent of at least a child under 18 years old
- No access to computer/laptop/mobile device or the Internet
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Maryland, College Park (Online Survey-Experiment)
College Park, Maryland, 20742, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Limitations and Caveats
The online survey-experiment may not fully reflect how individuals typically encounter health messages in the real world. There is concern about ecology validity. Also the long-term effects of message exposure were not determined.
Results Point of Contact
- Title
- Xiaoli Nan
- Organization
- University of Maryland, College Park
Study Officials
- PRINCIPAL INVESTIGATOR
Xiaoli Nan
University of Maryland, College Park
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 6, 2023
First Posted
July 25, 2023
Study Start
July 26, 2023
Primary Completion
August 8, 2023
Study Completion
August 8, 2023
Last Updated
October 21, 2024
Results First Posted
October 21, 2024
Record last verified: 2024-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- After the study is published, for 5 years.
- Access Criteria
- All information is open to the public.
We will share anonymized data on data repositories such as the Open Science Framework.