NCT05959564

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
456

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2023

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
19 days until next milestone

First Posted

Study publicly available on registry

July 25, 2023

Completed
1 day until next milestone

Study Start

First participant enrolled

July 26, 2023

Completed
13 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 8, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 8, 2023

Completed
1.2 years until next milestone

Results Posted

Study results publicly available

October 21, 2024

Completed
Last Updated

October 21, 2024

Status Verified

July 1, 2024

Enrollment Period

13 days

First QC Date

July 6, 2023

Results QC Date

July 23, 2024

Last Update Submit

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

EXPERIMENTAL

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).

Behavioral: Personalized Chatbot Intervention

Non-Personalized Chatbot Condition

EXPERIMENTAL

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.

Behavioral: Non-Personalized Chatbot Intervention

No Chatbot Control Condition

ACTIVE COMPARATOR

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

Behavioral: No Chatbot Control

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.

Personalized Chatbot Condition

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.

Non-Personalized Chatbot Condition

In this intervention, participants will see a standard CDC HPV vaccine message only and will not interact with any chatbot.

No Chatbot Control Condition

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Uterine Cervical NeoplasmsAnus NeoplasmsPenile Neoplasms

Condition Hierarchy (Ancestors)

Uterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by SiteNeoplasmsUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesRectal NeoplasmsColorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsDigestive System DiseasesGastrointestinal DiseasesIntestinal DiseasesAnus DiseasesRectal DiseasesGenital Neoplasms, MaleGenital Diseases, MalePenile DiseasesMale Urogenital Diseases

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

  • Xiaoli Nan

    University of Maryland, College Park

    PRINCIPAL INVESTIGATOR

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

We will share anonymized data on data repositories such as the Open Science Framework.

Shared Documents
STUDY PROTOCOL
Time Frame
After the study is published, for 5 years.
Access Criteria
All information is open to the public.

Locations