CClinicalTrials.gg
CompletedNCT02196454Updated Jun 1, 2018

Video to Promote HPV Vaccination

An interventional study of Educational Video with Male or Female Narrator in Vaccine Acceptance, Social Acceptance and Acceptance Processes, sponsored by Children's Hospital of Philadelphia. Completed at 2 sites in United States. Open to participants aged 11 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-06-01.

Sponsored by Children's Hospital of Philadelphia · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Randomized
Ages
11 Years and older
Sex
All
01

Study summary

The purpose of this research study is to determine if video-based education will increase HPV vaccination rates among 11 - 17 year olds.

Read the detailed description

Human Papillomavirus (HPV) is a common sexually transmitted infection that has the potential to cause cancer. The vaccine is recommended because it prevents the HPV infections that most commonly cause cancer. HPV vaccines offer the best protection to girls and boys who receive the complete, three-vaccine series and have time to develop an immune response before being exposed to HPV. However, vaccination rates are low compared to other vaccines for teens.

Results from this study will help us learn why participants do or do not get the HPV vaccination and whether video-based education can help improve vaccination rates

02

Conditions studied

  • Vaccine Acceptance
  • Social Acceptance
  • Acceptance Processes
  • Health Behavior
  • Human Papillomavirus

Keywords

  • HPV vaccine
  • vaccination
  • immunization
  • video
  • health education
  • communication
03

In context

Lead sponsor

Children's Hospital of Philadelphia is the lead sponsor of 480 studies on the registry; 85 are open to participants now.

Of its 28 completed or terminated interventional studies of FDA-regulated products, 22 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
11 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Parent-child dyads in which the child is a male or female age 11 to 17 years who has not received the HPV vaccine

Exclusion criteria

Exclusion Criteria:

  • Parent-child dyads in which the child has received the HPV vaccine
  • Parent-child dyads in which the child is older than 18 at the time of enrollment
  • Non-English speakers
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
110 participants (actual)

Study arms

  • No intervention
    Vaccine Information Statement

    Study participants will receive the HPV Vaccine Information Statement (VIS) which is part of routine care.

  • Experimental
    Video & Vaccine Information Statement

    Participants will view an educational video about the HPV vaccine with a male or female narrator. Participants will also receive the HPV Vaccine Information Statement (VIS) which is part of routine care.

    Other: Educational Video with Male or Female Narrator

Interventions

  • OtherEducational Video with Male or Female Narrator

    Participants will watch an educational video about the quadrivalent HPV vaccine (Gardasil) narrated by either a male or female.

06

What researchers measure

Primary outcomes

  1. HPV Vaccination Series Initiation

    Number of HPV vaccine doses received among study participants

    Time frame: 90 days

  2. HPV Vaccine Series Initiation

    HPV Vaccine Receipt among study participants

    Time frame: 0 days

Secondary outcomes

  1. HPV Vaccine Series Initiation (depending on male versus female narrator)

    Difference in rate of HPV vaccine receipt between study participants who viewed a video narrated by a male versus a female

    Time frame: 0 days

  2. HPV Vaccine Series Initiation (depending on male versus female narrator)

    Difference in number of HPV vaccine doses between study participants who viewed a video narrated by a male versus a female

    Time frame: 90 days

Other outcomes

  1. HPV Vaccine Awareness

    Reported reason for HPV vaccine receipt or deferral

    Time frame: 0 days

07

Study locations

2 sites
  • Primary Care, Flourtown, Children's Hospital of Philadelphia
    Flourtown, Pennsylvania 19031, United States
  • Nicholas and Athena Karabots Pediatric Care Center
    Philadelphia, Pennsylvania 19139, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 1, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02196454
Lead sponsor
Children's Hospital of Philadelphia
Collaborators
Noble Medical, LLC
Responsible party
Sponsor
First posted
Jul 22, 2014
Start date
Jul 2014
Primary completion
Dec 2016
Completion
May 31, 2018
Last update
Jun 1, 2018

Study contacts

Kristen A. Feemster, MD MPH MSHP
principal investigator · Children's Hospital of Philadephia

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2018. You cannot join it, but the record below documents what was studied.

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