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A Chatbot Intervention for Reducing HPV Vaccine Hesitancy

Primary Purpose

Cervical Cancer, Anal Cancer, Penile Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Personalized Chatbot Intervention
Non-Personalized Chatbot Intervention
No Chatbot Control
Sponsored by
University of Maryland, College Park
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cervical Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: 18 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 Exclusion Criteria: 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

Sites / Locations

  • University of Maryland, College Park (Online Survey-Experiment)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Personalized Chatbot Condition

Non-Personalized Chatbot Condition

No Chatbot Control Condition

Arm Description

After 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).

After 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.

Participants will read a standard CDC HPV vaccine message without interacting with any chatbot that delivers additional messages.

Outcomes

Primary Outcome Measures

Attitudes toward HPV vaccination
Participants' attitudes toward HPV vaccination will be measured by seven questions such as ""The HPV vaccine is beneficial for adolescents."
Intentions toward HPV vaccination
Participants' intentions toward vaccinating their children against HPV will be measured by three questions such as "I am likely to get my child/children the HPV vaccine."

Secondary Outcome Measures

Ratings of the Chatbot
Participants in the chatbot conditions will rate the chatbot on a number of characteristics such as engagingness, relevance, and trustworthiness.

Full Information

First Posted
July 6, 2023
Last Updated
August 17, 2023
Sponsor
University of Maryland, College Park
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1. Study Identification

Unique Protocol Identification Number
NCT05959564
Brief Title
A Chatbot Intervention for Reducing HPV Vaccine Hesitancy
Official Title
A Chatbot Intervention for Reducing HPV Vaccine Hesitancy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
July 26, 2023 (Actual)
Primary Completion Date
August 8, 2023 (Actual)
Study Completion Date
August 8, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Maryland, College Park

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.
Detailed Description
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 survey-experiment will be conducted. In the survey-experiment, participants will first answer questions related to their attitudes toward childhood vaccines and see a brief CDC message about HPV vaccine. Then they will be directed to interact with a chatbot designed to deliver personalized HPV vaccine messages (tailored to the participant's personality) or a similar chatbot with non-personalized messages. There will also be a control condition where participants will see the brief CDC message about HPV vaccine but will not interact with any chatbot. All participants will answer questions related to their attitudes toward HPV vaccination, intentions to vaccinate their children, as well as other message response measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer, Anal Cancer, Penile Cancer

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
456 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Personalized Chatbot Condition
Arm Type
Experimental
Arm Description
After 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).
Arm Title
Non-Personalized Chatbot Condition
Arm Type
Experimental
Arm Description
After 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.
Arm Title
No Chatbot Control Condition
Arm Type
Active Comparator
Arm Description
Participants will read a standard CDC HPV vaccine message without interacting with any chatbot that delivers additional messages.
Intervention Type
Behavioral
Intervention Name(s)
Personalized Chatbot Intervention
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Non-Personalized Chatbot Intervention
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
No Chatbot Control
Intervention Description
In this intervention, participants will see a standard CDC HPV vaccine message only and will not interact with any chatbot.
Primary Outcome Measure Information:
Title
Attitudes toward HPV vaccination
Description
Participants' attitudes toward HPV vaccination will be measured by seven questions such as ""The HPV vaccine is beneficial for adolescents."
Time Frame
Immediately after the intervention
Title
Intentions toward HPV vaccination
Description
Participants' intentions toward vaccinating their children against HPV will be measured by three questions such as "I am likely to get my child/children the HPV vaccine."
Time Frame
Immediately after the intervention
Secondary Outcome Measure Information:
Title
Ratings of the Chatbot
Description
Participants in the chatbot conditions will rate the chatbot on a number of characteristics such as engagingness, relevance, and trustworthiness.
Time Frame
Immediately after the intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 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 Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaoli Nan
Organizational Affiliation
University of Maryland, College Park
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Maryland, College Park (Online Survey-Experiment)
City
College Park
State/Province
Maryland
ZIP/Postal Code
20742
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We will share anonymized data on data repositories such as the Open Science Framework.
IPD Sharing Time Frame
After the study is published, for 5 years.
IPD Sharing Access Criteria
All information is open to the public.

Learn more about this trial

A Chatbot Intervention for Reducing HPV Vaccine Hesitancy

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