A Message Framing Intervention for Increasing Parental Acceptance of Human Papillomavirus Vaccination

NCT ID: NCT03856437

Last Updated: 2024-03-15

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

1170 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-22

Study Completion Date

2022-04-15

Brief Summary

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The goal of this study is to determine the effects of message framing (gain vs. loss) on African American parents' acceptance of the HPV vaccine and how such effects are moderated by parents' salient beliefs prior to message exposure. Participants are randomized into gain and loss conditions in which they view either gain-framed or loss-framed HPV vaccination messages. Key outcome variables include parents' attitudes and intentions toward vaccinating their children against HPV.

Detailed Description

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The goal of this study is to determine the effects of message framing (gain vs. loss) on African American parents' acceptance of the HPV vaccine and how such effects are moderated by parents' salient beliefs prior to message exposure. Participants recruited from local communities and online panels will complete a computer-assisted survey. In the survey participants will first answer questions related to their beliefs about HPV and the HPV vaccine (e.g., perceived susceptibility, perceived severity, perceived efficacy, perceived safety, etc.), as well as other background information. Then they will be presented with either a gain-framed or loss-framed human papillomavirus vaccination message. After the message exposure, they will answer questions related to their attitudes toward HPV vaccination, intentions to vaccinate their children, as well as other message response measures. Eligible participants are at least 21 years old, self-identify as African American, and are custodial parents or caretakers of at least one child ages 9-17 who has not initiated the HPV vaccine series.

Conditions

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Cervical Cancer Anal Cancer Penile Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Gain-framed messages

Participants in this arm receive gain-framed HPV vaccination messages.

Group Type EXPERIMENTAL

HPV vaccination messages

Intervention Type BEHAVIORAL

Digital multimedia messages consisting of text and imagery conveying the benefits of being vaccinated against HPV, the costs of not being vaccinated against HPV, or neither benefits or costs but simply a call for action.

Loss-framed messages

Participants in this arm receive loss-framed HPV vaccination messages.

Group Type EXPERIMENTAL

HPV vaccination messages

Intervention Type BEHAVIORAL

Digital multimedia messages consisting of text and imagery conveying the benefits of being vaccinated against HPV, the costs of not being vaccinated against HPV, or neither benefits or costs but simply a call for action.

Control messages

Participants in this arm receive non-framed HPV vaccination messages.

Group Type ACTIVE_COMPARATOR

HPV vaccination messages

Intervention Type BEHAVIORAL

Digital multimedia messages consisting of text and imagery conveying the benefits of being vaccinated against HPV, the costs of not being vaccinated against HPV, or neither benefits or costs but simply a call for action.

Interventions

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HPV vaccination messages

Digital multimedia messages consisting of text and imagery conveying the benefits of being vaccinated against HPV, the costs of not being vaccinated against HPV, or neither benefits or costs but simply a call for action.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 18 years or older
* Self-identify as African American
* Custodial parent or caretaker of at least one child under the age of 18 who has not been fully vaccinated against HPV.
* Has access to Internet to complete the study

Exclusion Criteria

* Younger than 18 years
* Does not self-identify as African American
* Not a custodial parent or caretaker of at least one child under the age of 18 who has not been fully vaccinated against HPV.
* Has no access to Internet to complete the study
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

University of Maryland, College Park

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Xiaoli Nan

Role: PRINCIPAL_INVESTIGATOR

University of Maryland, College Park

Locations

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University of Maryland

College Park, Maryland, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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R01CA219060

Identifier Type: NIH

Identifier Source: secondary_id

View Link

1322177-1.1

Identifier Type: -

Identifier Source: org_study_id

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