Gardasil Administration

Not Applicable

Withdrawn

• Conditions: Vaccine Administration Rates
• Interventions: Behavioral: Appointment reminders

• Registration Number: NCT03123419
• Lead Sponsor: St. Louis University

Brief Summary

The purpose of the Gardasil study is to increase the rates of Gardasil vaccination at a maternal fetal Care Center. This will be done by reminding patients via text to come for follow up vaccine appointments.

Detailed Description

Patients will be screened in center for history of Gardasil vaccination. If the patient has not received the vaccination series they will be counseled/educated (standard of care \[SOC }) and offered the vaccine series. If the patient agrees to the vaccination, they will then be offered participation in this study, (consent will be reviewed and signed) and they will receive the first vaccination at this visit, administered according to standard protocol. The patient will then be scheduled for two follow up vaccination appointments. The second vaccination will be given 2 months after the first vaccine and the third will be given 4 months after the second vaccination in accordance with the Gardasil vaccine guidelines. -SOC

The patients will receive a total of two texts during the study entirety. The two texts will be appointment reminders for the second and third vaccination, sent 1 week prior to the next appointment. This is study related.

Data collection Data will be collected using a data collection sheet. The investigators will record date of first vaccine administration and adherence to follow up.vaccinations.

Study Timeline

• Study First Submitted: 2017-04-10
• Study First Submitted QC: 2017-04-18
• Study First Posted: 2017-04-21
• Study Start: 2018-02-01
• Status Verified: 2018-03
• Last Update Submitted: 2018-03-05
• Last Update Posted: 2018-03-07
• Primary Completion: 2019-03-01
• Study Completion: 2019-04-01

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Vaccine	Appointment reminders	All patients who consent to be in the study will receive Appointment reminders.

Primary Outcome Measures

Name	Time	Method
Increase HPV-9 vaccine administration rates	through study completion, an average of 1 year	The text reminder messages will increase HPV-9 vaccine administration rates

Trial Locations

Locations (1)

St. Mary's Health Center; 🇺🇸 Saint Louis, Missouri, United States