Human Papilloma Virus Clinical Trial
Official title:
Increasing Human Papillomavirus (HPV) Vaccine Uptake Via General Health Messaging
NCT number | NCT03759236 |
Other study ID # | 48789 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 25, 2018 |
Est. completion date | February 19, 2020 |
Verified date | February 2020 |
Source | University of California, Los Angeles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Prevention of cervical cancer and genital warts could be achieved by immunization
with the prophylactic human papillomavirus (HPV) vaccines commercially available. However, in
the U.S. only 38% of females and 14% of males in the recommended age group (9-26 years)
receive the complete, three-dose HPV vaccine. Because the HPV vaccine is covered under the
Vaccine for Children Program, the underinsured and uninsured have no-cost access.
Nonetheless, data from Los Angeles county suggest that HPV vaccination rates among the
uninsured and underinsured groups are significantly lower than the national average, likely
related to knowledge of the vaccine, transportation, number of doses and concern of side
effects.
Aim: To evaluate the efficacy of health oriented text messaging to increase HPV vaccine
uptake versus standard health messaging (Center for Disease Control and Prevention (CDC) HPV
vaccine information flyers).
Hypothesis: The investigators hypothesize that receiving general health messaging, including
messages regarding the benefits of the HPV vaccine, will increase HPV vaccine uptake. Text
messaging will also be more successful in reaching the uninsured and underinsured populations
than will traditional flyers/information pamphlets used in clinics.
Methods: A cluster randomized trial design will be used to recruit participants from four
clinics in Los Angeles County which offer pediatric vaccination to uninsured and underinsured
children. The sample will include women aged 18-45 years of age. Two of the sites will be
randomized to the text messaging arm and the other clinic will be randomized to the control
arm (standard messaging: CDC flyers and pamphlets available for patients at the clinic).
Outcome measures will be HPV vaccinations rates at those clinics. Rates will be defined into
groups who received 1 dose, 2 doses and 3 doses.
Anticipated Results: The investigators expect to find statistically significant higher HPV
vaccination rates among children and women in the text messaging study arm compared to the
control arm.
Implications and Future Studies: This pilot study will give us preliminary data to submit a
larger randomized controlled trial to examine the efficacy of text messaging.
Status | Completed |
Enrollment | 3 |
Est. completion date | February 19, 2020 |
Est. primary completion date | February 19, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Women who are patients at the clinic - Age 18+ - Have a working mobile phone with SMS capability Exclusion Criteria: - Male - <18 years of age - Do not have a working mobile phone with SMS capability |
Country | Name | City | State |
---|---|---|---|
United States | University of California Los Angeles | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Los Angeles | Cedars-Sinai Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | HPV Vaccination Rate | In both arms of the study, we will collect data on the number of females aged 9- 26 years who made any visit to the clinic (denominator) and the number of females aged 9-26 vaccinated (numerator). Vaccination rates will be defined into groups who received at least 1 dose, compared to receiving none. We will also examine those receiving at least 2 doses vs 1 vs none. | 1 year |
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