Interactive, Health Literacy Promoting Text Messages and HPV Vaccine Completion In Minority Adolescents
- Conditions
- Human Papillomavirus
- Registration Number
- NCT02236273
- Lead Sponsor
- Columbia University
- Brief Summary
Emerging communication technologies, such as text messaging offer low-cost, scalable opportunities to improve health literacy and promote healthy behaviors, such as vaccination. While the investigators reported the success of text message vaccine reminders, effects were limited by their untailored approach. The trans-theoretical model of behavior change supports tailoring interventions to an individual's stage of decision-making. Human papillomavirus (HPV) is the most prevalent sexually transmitted virus in the U.S. and can lead to genital warts, and cervical, anal and penile cancer. The three-dose vaccine is 90-100% efficacious. Minorities are at greatest risk for such cancers but have low HPV vaccine completion rates. Limited health literacy regarding the vaccine can affect series completion. The investigators will compare the effects of enhancing text message vaccination reminders with interactive, vaccine health literacy-promoting information tailored to vaccine decision making-stage on HPV vaccine series completion. The effects of these messages represent a new paradigm in interactive health communications.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 956
- Parenting adult of adolescent age 11-17 years
- Adolescent received 1st dose of HPV at a study site within the last 2 weeks.
- Eligible parent's cell phone has text message capability
- Language other than English or Spanish only
- Parent already in the study
- Intends to move away from the New York City area in <12 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Number of Participants Who Completed HPV Vaccine Series 12 months receipt of 3 doses of HPV vaccine by 12 months after initiation
- Secondary Outcome Measures
Name Time Method Time Between 1st and 2nd Dose 12 months Time elapsed in days between first and second dose- for those in need of three doses
Time Between 1st and 3rd Dose 12 months Time elapsed (in days) between 1st and 3rd dose for those in need of three doses
Related Research Topics
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Trial Locations
- Locations (1)
Columbia University Medical Center
🇺🇸New York, New York, United States
Columbia University Medical Center🇺🇸New York, New York, United States