- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02231957
Text Message Vaccine Reminders for Adolescents With Chronic Medical Conditions
January 27, 2017 updated by: Annika Hofstetter, Columbia University
There are a growing number of adolescents with chronic medical conditions in the United States.
The Advisory Committee on Immunization Practices (ACIP) recommends HPV vaccination and annual influenza vaccination of all adolescents.
Pneumococcal polysaccharide vaccination is also recommended for certain high-risk patients.
Limited studies suggest that vaccination coverage of this population remains sub-optimal.
Text message vaccine reminder/recall has been shown to be effective in increasing uptake of select pediatric and adolescents vaccines, but has yet to be examined among patients with chronic medical conditions who may also face unique barriers to vaccination.
This intervention aims to implement and evaluate the use of text message vaccine reminders among urban low-income minority adolescents with chronic medical conditions.
This investigator-initiated study is supported in part by a grant from the Pfizer Medical Education Group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
416
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10032
- NewYork-Presbyterian Hospital/Columbia University Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
11 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Parent with
- adolescent aged 11-17 years;
- adolescent with ≥1 chronic medical condition;
- adolescent with clinic visit in last 12 months;
- cell phone number listed in hospital registration system
Exclusion Criteria:
Parent who:
- does not speak English or Spanish;
- is unwilling to receive text message vaccine reminders;
- anticipates moving from area in coming 12 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: educational text message reminders
receipt of education-embedded text message vaccine reminders
|
Other Names:
|
|
Active Comparator: conventional text message reminders
receipt of conventional text message vaccine reminders
|
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Percentage of eligible subjects who received HPV1, influenza, and/or pneumococcal vaccine(s)
Time Frame: 12 weeks after intervention start
|
12 weeks after intervention start
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Percentage of eligible subjects who received HPV1, influenza, and/or pneumococcal vaccine(s)
Time Frame: 4 weeks after intervention start
|
4 weeks after intervention start
|
|
Percentage of eligible subjects who received HPV1, influenza, and/or pneumococcal vaccine(s)
Time Frame: 24 weeks after intervention start
|
24 weeks after intervention start
|
|
Percentage of eligible subjects with missed opportunities for HPV1, influenza, and/or pneumococcal vaccination
Time Frame: 4 weeks after intervention start
|
4 weeks after intervention start
|
|
Percentage of eligible subjects with missed opportunities for HPV1, influenza, and/or pneumococcal vaccination
Time Frame: 12 weeks after intervention start
|
12 weeks after intervention start
|
|
Percentage of eligible subjects with missed opportunities for HPV1, influenza, and/or pneumococcal vaccination
Time Frame: 24 weeks after intervention start
|
24 weeks after intervention start
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Annika M Hofstetter, MD, PhD, MPH, Columbia University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2014
Primary Completion (Actual)
June 1, 2015
Study Completion (Actual)
January 1, 2017
Study Registration Dates
First Submitted
August 15, 2014
First Submitted That Met QC Criteria
September 2, 2014
First Posted (Estimate)
September 4, 2014
Study Record Updates
Last Update Posted (Estimate)
January 30, 2017
Last Update Submitted That Met QC Criteria
January 27, 2017
Last Verified
January 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AAAM3756
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Vaccination
-
University of Massachusetts, WorcesterRecruiting
-
University of TorontoWholehealth Pharmacy PartnersNot yet recruitingVaccination | Vaccination Reaction | Vaccination Pain | Vaccination PharmacyCanada
-
University of Roma La SapienzaCompletedVaccination Failure | Vaccination Adverse Events | Specific Antibody ResponseItaly
-
University of IowaNational Institute on Aging (NIA)CompletedVaccination | Vaccination Hesitancy | Vaccination Promotion | Psychological AspectsUnited States
-
Xiamen UniversityXiamen Center for Disease Control and PreventionNot yet recruitingHPV Vaccination Rates | HPV Vaccine Awareness | HPV Vaccination Intention
-
National Cancer Institute (NCI)CompletedHPV16 Anitbody Levels Post Vaccination | HPV18 Antibody Levels Post VaccinationUganda
-
Université de Reims Champagne-ArdenneRecruiting
-
University of EssexUniversity of Southern California; Kingston University; Department of Health...Completed
-
China National Biotec Group Company LimitedPeking University; Beijing Institute of Biological Products Co Ltd.; Sichuan... and other collaboratorsCompleted
-
China National Biotec Group Company LimitedSichuan Center for Disease Control and PreventionCompleted
Clinical Trials on educational text message reminders
-
Stanford UniversityCompletedCeliac DiseaseUnited States
-
University of RochesterRecruitingProstate Cancer | Benign Prostate Hyperplasia | Incontinence, Urinary StressUnited States
-
Children's Hospital of PhiladelphiaCompletedPelvic Inflammatory DiseaseUnited States
-
University of Texas Southwestern Medical CenterUniversity of California, DavisCompleted
-
Harvard School of Public Health (HSPH)Completed
-
Wake Forest University Health SciencesCompleted
-
Children's Hospitals and Clinics of MinnesotaUnknownMental Health Disorder | Mental and Behavioral Disorder | Self-inflicted Injury
-
Children's Hospital Medical Center, CincinnatiCMSTextCompleted
-
Wayne State UniversityAgency for Healthcare Research and Quality (AHRQ)CompletedHypertensionUnited States
-
University of Texas Southwestern Medical CenterCompletedSuicideUnited States