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Provider Training + Interactive Texting for HPV Vaccination (Text&Talk Trial)

N/A
Waitlist Available
Led By Stephanie Staras, PhD
Research Sponsored by University of Florida
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights

Text&Talk Trial Summary

This trial will test if sending texts or training clinicians can increase HPV vaccination rates for 11-12 year olds in Florida.

Who is the study for?
This trial is for parents of 10- to 12-year-olds who haven't had the HPV vaccine and visit participating Florida clinics. It's also for providers giving primary care to this age group at these clinics. Adolescents outside this age range, those opted-out of texts, or without a cell number on file can't join.Check my eligibility
What is being tested?
The study tests two methods to increase HPV vaccination rates: one sends educational text messages to parents, and the other provides brief training to clinicians. The goal is to see if these approaches encourage vaccinations in 11-12 year olds.See study design
What are the potential side effects?
Since the interventions involve education and communication rather than medical treatments, there are no direct side effects from medications or procedures. However, participants may experience an increased volume of communications.

Text&Talk Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Initiation of the HPV Vaccine
Up to date for the HPV Vaccine
Secondary outcome measures
Frequency of Provider recommendations
Other outcome measures
Visited the clinic

Text&Talk Trial Design

9Treatment groups
Experimental Treatment
Active Control
Group I: Deferred-clinician training and bundled text messagesExperimental Treatment1 Intervention
Clinicians will receive training after the study and parents will receive bundled text messages.
Group II: Deferred-clinician training and benefits text messagesExperimental Treatment1 Intervention
Clinicians will receive training after the study and parents will receive benefits text messages.
Group III: Bundled clinician training and no text messagesExperimental Treatment1 Intervention
Clinicians will receive bundled approach training and parents will not receive any intervention text messages.
Group IV: Bundled clinician training and bundled text messagesExperimental Treatment2 Interventions
Clinicians will receive bundled approach training and parents will receive bundled text messages.
Group V: Bundled clinician training and benefits text messagesExperimental Treatment2 Interventions
Clinicians will receive bundled approach training and parents will receive benefits text messages.
Group VI: Benefits clinician training and no text messagesExperimental Treatment1 Intervention
Clinicians will receive benefits approach training and parents will not receive any intervention text messages.
Group VII: Benefits clinician training and bundled text messagesExperimental Treatment2 Interventions
Clinicians will receive benefits approach training and parents will receive bundled text messages.
Group VIII: Benefits clinician training and benefits text messagesExperimental Treatment2 Interventions
Clinicians will receive benefits approach training and parents will receive benefits text messages.
Group IX: Deferred-clinician training and no text messagesActive Control1 Intervention
Clinicians will receive training after the study and parents will not receive intervention text messages.

Find a Location

Who is running the clinical trial?

National Cancer Institute (NCI)NIH
13,654 Previous Clinical Trials
40,912,043 Total Patients Enrolled
University of FloridaLead Sponsor
1,340 Previous Clinical Trials
694,586 Total Patients Enrolled
Stephanie Staras, PhDPrincipal InvestigatorUniversity of Florida
3 Previous Clinical Trials
7,034 Total Patients Enrolled

Media Library

Bundled clinician training and benefits text messages Clinical Trial Eligibility Overview. Trial Name: NCT05006833 — N/A
Human Papillomavirus Research Study Groups: Bundled clinician training and benefits text messages, Bundled clinician training and no text messages, Benefits clinician training and no text messages, Deferred-clinician training and bundled text messages, Benefits clinician training and benefits text messages, Deferred-clinician training and benefits text messages, Bundled clinician training and bundled text messages, Benefits clinician training and bundled text messages, Deferred-clinician training and no text messages
Human Papillomavirus Clinical Trial 2023: Bundled clinician training and benefits text messages Highlights & Side Effects. Trial Name: NCT05006833 — N/A
Bundled clinician training and benefits text messages 2023 Treatment Timeline for Medical Study. Trial Name: NCT05006833 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are we enrolling people in this research project at the moment?

"That is correct. Currently, this trial is recruiting patients as the most recent update on clinicaltrials.gov was on 6/30/2022. The study requires 21110 individuals from 2 locations and it was initially posted 11/18/2021."

Answered by AI

What is the total number of participants for this research project?

"That is correct, the online clinicaltrial.gov registry shows that this study is recruiting patients. The listing was first made on November 18th, 2021 and updated as recently as June 30th, 2022. They are looking for a total of 21110 people to participate at 2 sites."

Answered by AI
~5413 spots leftby Feb 2025