Text Message Reminder-Recalls For Early Childhood Vaccination
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Purpose
Although the investigators have reached the Healthy People 2010 goal of 80% coverage among U.S. children 19-35 months of age for the primary immunization series, 20% of children still remain underimmunized. In addition, pockets of low immunization coverage and outbreaks of vaccine preventable disease persist. Immunization reminder-recalls have been shown to be successful, but have been limited by the ability to identify and reach large target populations in a real-time, automated fashion. Reminder-recalls via text message may offer an innovative opportunity to improve vaccination coverage. Currently, 91% of Americans own a cell phone. Prior research by our team suggests that text messages reminder recalls may be an effective tool to remind parents about their children's vaccines. In this study, the investigators will demonstrate the effectiveness of tailored text message appointment and immunization reminders linked to a well-established and functional immunization registry to increase coverage rates and timeliness of the sentinel vaccines of MMR and HepA. The investigators will target parents of young children from an underserved population that is primarily Latino, with low socioeconomic status.
| Condition | Intervention |
|---|---|
|
Vaccination |
Other: Text message |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single Blind (Investigator) Primary Purpose: Health Services Research |
| Official Title: | Text 4 Health-Kids: Text Message Reminder-Recalls For Early Childhood Vaccination |
- Receipt of MMR1 [ Time Frame: by 13 and 16 months of age ] [ Designated as safety issue: No ]
- Timeliness of HepA vaccination post-recall [ Time Frame: 4,12, 24 weeks ] [ Designated as safety issue: No ]
- Attendance at appointments [ Time Frame: after appointment ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 3908 |
| Study Start Date: | June 2011 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | June 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Text message reminders |
Other: Text message
text message appointment and immunization reminders
|
|
Active Comparator: standard of care for MMR, letter reminder for Hep A
MMR: automated phone call appointment reminder Hep A: recall letter, automated phone call appointment reminder
|
Other: Text message
text message appointment and immunization reminders
|
Eligibility| Ages Eligible for Study: | 9 Months to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Parents of child >9 months to 25 months
- Child with at least one visit to one of the participating clinical sites in the previous 12 months
- Parental cell phone number recorded in the registration system
Contacts and Locations| Contact: Melissa S Stockwell, MD MPH | 212-342-5732 | mstockwell@columbia.edu |
| United States, New York | |
| Columbia University Medical Center | Recruiting |
| New York, New York, United States, 10032 | |
| Contact: Melissa S Stockwell, MD MPH 212-342-5732 mstockwell@columbia.edu | |
| Principal Investigator: Melissa S Stockwell, MD MPH | |
| Sub-Investigator: Annika Hofstetter, MD PHD MPH | |
| Principal Investigator: | Melissa S Stockwell, MD MPH | Columbia University |
| Study Director: | Annika Hofstetter, MD PhD MPH | Columbia University |
More Information
No publications provided
| Responsible Party: | Melissa Stockwell, MD, MPH, Asst Prof of Pediatrics and Population and Family Health, Columbia University |
| ClinicalTrials.gov Identifier: | NCT01199666 History of Changes |
| Other Study ID Numbers: | AAAF4263 |
| Study First Received: | September 9, 2010 |
| Last Updated: | February 11, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Columbia University:
|
Underimmunization, text message, vaccination Underimmunization |
ClinicalTrials.gov processed this record on May 21, 2013