Text Reminders for Immunization Compliance in Kids (TRICKS) Pilot Study

March 9, 2012 updated by: Carolyn R. Ahlers-Schmidt, PhD, University of Kansas

Text Reminders for Immunization Compliance in Kids

As a participant in these research program you will be a parent of a child born at Wesley Medical Center who plan to use Carriage Park Pediatric Clinic for your child's care. Mobile phone text messages will be sent to remind you of your child's immunizations.

The long term research goal is to increase childhood immunization rates by improving parental health literacy through an innovative text messaging system regarding immunization schedules for children under the age of six.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

90

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

    • Kansas
      • Wichita, Kansas, United States, 67214
        • Kansas University School of Medicine-Wichita

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • parent or caregiver of a well child born at Wesley Medical Center;
  • planning to utilize the Carriage Park Pediatric Clinic for his/her child's medical home; (
  • adult (> 18 years of age);
  • present use of a mobile phone for sending and receiving text messages;
  • English or Spanish speaking;
  • able to provide informed consent.

Exclusion criteria include:

  • personal or religious beliefs against immunizations;
  • inability to complete enrollment information.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Standard of care
You will receive an immunization handout and verbal instructions regarding your child's next apt. Your child's immuniztion records will also be checked through KSWebIZ an internet based system that tracks immunizations for kids in Kansas.
Experimental: Text Messaging
You will receive text message reminders prior to your child's two, four and six month immunization due dates. You will be asked to take part in a phone interview and your child's immuniztion records will be checked through KSWebIZ an internet based system that tracks immunizations for kids in Kansas.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the first aim is to assess our ability to enroll at least 70% (N=90) of eligible parents in a text messaging program
Time Frame: up to 1 year
This will be accomplished through recruitment of parents of newborns at Wesley Medical Center who will receive care from Carriage Park Clinic.
up to 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the second aim is to implement the TRICKs intervention with parents of newborns.
Time Frame: up to 1 year
SMSCaster software will be assessed for its ability to send appointment reminders and to collect follow-up data from parents regarding whether immunization appointments were scheduled.
up to 1 year
the third aim is to collect immunization information on participant's children.
Time Frame: up to 1 year
This will be accomplished using the Kansas Immunization Registry (KSWebIZ), a web-based centralized birth to death database that maintains complete, accurate, and secure immunization records for all Kansas residents.
up to 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

July 1, 2010

Primary Completion (Actual)

December 1, 2011

Study Completion (Actual)

December 1, 2011

Study Registration Dates

First Submitted

July 17, 2011

First Submitted That Met QC Criteria

July 18, 2011

First Posted (Estimate)

July 19, 2011

Study Record Updates

Last Update Posted (Estimate)

March 12, 2012

Last Update Submitted That Met QC Criteria

March 9, 2012

Last Verified

March 1, 2012

More Information

Terms related to this study

Other Study ID Numbers

  • 10-018

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.

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