- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05204030
Hashtag HPV: HPV Vaccine Twitter Education Program
January 26, 2023 updated by: University of Arkansas, Fayetteville
Hashtag HPV: Engaging Parents Through Social Media to Increase HPV Vaccination
Parents use social media as an important parenting tool and source for health information.
Using social media data to examine public opinion has had an early impact in public health and in cancer control and prevention efforts, including about the human papillomavirus (HPV) vaccine.
A next step in this area of research is to develop and share messages on social media with parents to help inform and educate them about the HPV vaccine - ultimately assisting them with their decision to vaccinate their child.
This study will evaluate the efficacy of social media messages through Twitter, using a randomized controlled trial to determine what types of messages resonate with parents.
The investigators will examine differences between two types of messages - narrative messages (i.e., stories) and non-narrative messages (i.e., numbers and facts).
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Detailed Description
Approximately 80 million people in the United States - or about one in four - are infected with human papillomavirus (HPV).
HPV can cause cancer and there are vaccines that protect against cancer-related strains.
Evidence supporting vaccine efficacy and safety is robust, and vaccine availability is widespread; however coverage rates continue to fall short of the national goal of 80% (48.6% in 2017).
Understanding the barriers to vaccine acceptance, particularly related to parent resistance and their informational needs, is key to strengthening vaccine uptake among adolescents.
Communicating evidence to parents and engaging them through narrative strategies may address some of the barriers during the decision-making process.
Parents use social media as an important parenting tool and useful source for health information.
In 2015, 75% of all parents used social media, and of these 1 in 4 used Twitter - equating to millions of parent users.
The investigators know that using social media data for surveillance has had early impact in public health.
However, what is not known is the effectiveness of using large-scale social media data to inform a targeted social media intervention to support HPV vaccine uptake.
This study will advance the growing field by evaluating the efficacy of an innovative narrative-focused intervention designed to communicate evidence and information about the HPV vaccine for parents who use social media as a health information source.
The approach is informed by narrative engagement theory that posits narratives strengthen knowledge and promote engagement through storytelling by tapping into feelings of empathy, identification, and transportation.
The investigators will evaluate the efficacy of our Twitter-based pilot intervention in a randomized controlled trial that will enroll 600 parents/caregivers of children ages 9-14, whose child(ren) has not started the vaccine series.
Our central hypothesis is that exposure to narrative-focused exemplar messages will lead to greater intention to vaccinate, and subsequently increased rates of vaccination in the intervention group compared to parents in the comparison group, who receive non-narrative HPV vaccine information (i.e., existing HPV vaccine information developed for Twitter).
The investigators will use a Twitter-based Community Advisory Board, virtual focus groups, and existing Twitter messages developed by the HPV Roundtable to inform narrative-focused message development.
The proposed study will address three specific aims: 1) Develop narrative-focused scientific exemplars for HPV vaccine communication utilizing existing online messages and community engagement on Twitter; 2) Quantify differences in engagement, intention to vaccinate, and self-reported vaccination between parents exposed to the narrative-focused scientific exemplars and parents exposed to non-narrative scientific messages; 3) Collect and analyze longitudinal participant metadata to measure Twitter activity during the study period.
This study will impact the field of cancer prevention generally and HPV vaccination specifically by establishing the efficacy of narrative-focused health messaging campaign on social media, using a Twitter-based parent-engagement strategy.
Study Type
Interventional
Enrollment (Anticipated)
600
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Arkansas
-
Fayetteville, Arkansas, United States, 72701
- University of Arkansas
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria: The study population includes parents who have children ages 9-14. All participants will be 18 years of age or older, and we will specifically target parents ages 25 and older. Eligibility for enrollment in the study will be limited to the following criteria:
- Adults 18 years of age and older;
- Utilizes Twitter, a social media platform;
- Has a child aged 9-14;
- Child has not started the 2-dose HPV vaccination series;
- Has no child who has completed any dose HPV vaccination series;
- Has a well-care visit scheduled for their child before December, 2022.
Exclusion Criteria:
- Any adult who does not have a child 9-14 years of age;
- Any adult who does not indicate some level of participation in Twitter;
- Any adults who indicates a high level of anti-vaccine sentiment (assessed by vaccine hesitancy questions asked in the screener).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Narrative
The intervention condition will present narrative-focused messages about HPV and the HPV vaccine that includes important parent focused exemplar language and cultural norms on Twitter told through stories and characters (i.e., pseudo-parents).
|
This study will evaluate the efficacy of social media messages through Twitter, using a randomized controlled trial to determine what types of messages resonate with parents.
The investigators will examine narrative messages (i.e., stories).
The central hypothesis is that parents who read narrative-focused messages will be more likely to report narrative engagement, intention to vaccinate their child, and self-reported vaccination compared to parents who read non-narrative messages.
|
|
Active Comparator: Non-Narrative
The non-narrative condition will present scientific-focused messages about HPV and the HPV vaccine that includes important information relayed with numbers and facts.
|
This study will evaluate the efficacy of social media messages through Twitter, using a randomized controlled trial to determine what types of messages resonate with parents.
The investigators will examine non-narrative messages (i.e., scientific information - numbers and facts).
The central hypothesis is that parents who read narrative-focused messages will be more likely to report narrative engagement, intention to vaccinate their child, and self-reported vaccination compared to parents who read non-narrative messages.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in caregiver self-reported HPV vaccination status of child questionnaire
Time Frame: Change in caregiver self-reported HPV vaccination of child at 1-month follow-up from baseline
|
dependent variable; measure collects date of vaccination and number of vaccine doses to date
|
Change in caregiver self-reported HPV vaccination of child at 1-month follow-up from baseline
|
|
Change in caregiver self-reported HPV vaccination status of child questionnaire
Time Frame: Change in caregiver self-reported HPV vaccination of child at 1-year follow-up from 1-month follow-up
|
dependent variable; measure collects date of vaccination and number of vaccine doses to date
|
Change in caregiver self-reported HPV vaccination of child at 1-year follow-up from 1-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Caregiver self-reported empathy subscale adapted from Busselle & Bilandzic (2009) and Murphy, Frank, Chatterjee, Baezconde-Garbanati (2013).
Time Frame: only at 1-month post intervention
|
mediating/moderating variable
|
only at 1-month post intervention
|
|
Caregiver self-reported transportation subscale adapted from Murphy, Frank, Chatterjee, Baezconde-Garbanati (2013). Narrative versus Non-narrative: The Role of Identification, Transportation and Emotion in Reducing Health Disparities.
Time Frame: only at 1-month post intervention
|
mediating/moderating variable
|
only at 1-month post intervention
|
|
Caregiver self-reported identification subscale adapted from Murphy, Frank, Chatterjee, Baezconde-Garbanati (2013). Narrative versus Non-narrative: The Role of Identification, Transportation and Emotion in Reducing Health Disparities.
Time Frame: only at 1-month post intervention
|
mediating/moderating variable
|
only at 1-month post intervention
|
|
Change in caregiver self-reported intention to vaccinate their child questionnaire
Time Frame: Change in caregiver self-reported intention to vaccinate their child at 1-month follow-up from baseline
|
dependent variable; measures readiness and likeliness to receive HPV vaccination
|
Change in caregiver self-reported intention to vaccinate their child at 1-month follow-up from baseline
|
|
Change in caregiver self-reported intention to vaccinate their child questionnaire
Time Frame: Change in caregiver self-reported intention to vaccinate their child at 1-year follow-up from 1-month follow-up
|
dependent variable; measures readiness and likeliness to receive HPV vaccination
|
Change in caregiver self-reported intention to vaccinate their child at 1-year follow-up from 1-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: Philip M Massey, PhD, MPH, University of California, Los Angeles
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Massey PM, Kearney MD, Hauer MK, Selvan P, Koku E, Leader AE. Dimensions of Misinformation About the HPV Vaccine on Instagram: Content and Network Analysis of Social Media Characteristics. J Med Internet Res. 2020 Dec 3;22(12):e21451. doi: 10.2196/21451.
- Massey PM, Togo E, Chiang SC, Klassen AC, Rose M, Manganello JA, Leader AE. Identifying HPV vaccine narrative communication needs among parents on social media. Prev Med Rep. 2021 Jul 7;23:101488. doi: 10.1016/j.pmedr.2021.101488. eCollection 2021 Sep.
- Massey PM, Chiang SC, Rose M, Murray RM, Rockett M, Togo E, Klassen AC, Manganello JA, Leader AE. Development of Personas to Communicate Narrative-Based Information About the HPV Vaccine on Twitter. Front Digit Health. 2021 Aug 4;3:682639. doi: 10.3389/fdgth.2021.682639. eCollection 2021.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 13, 2021
Primary Completion (Anticipated)
August 30, 2023
Study Completion (Anticipated)
August 30, 2023
Study Registration Dates
First Submitted
December 9, 2021
First Submitted That Met QC Criteria
January 10, 2022
First Posted (Actual)
January 24, 2022
Study Record Updates
Last Update Posted (Estimate)
January 30, 2023
Last Update Submitted That Met QC Criteria
January 26, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2108351667
- 7R01CA229324-04 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
There is not a plan to make IPD available.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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