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Making Decisions About the Measles-Mumps-Rubella Vaccine

Primary Purpose

Measles, Mumps, Rubella

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Behavioral: Computer-based tailoring system
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Measles focused on measuring Measles, Mumps, Rubella, MMR, Prevention, Tailoring, Persuasive communication, Children

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Parent is greater than or equal to 18 years of age
  • Parent has a child 6 years of age or younger
  • When asked to describe how he/she feels about getting child vaccinated against MMR, parent responds "I don't want to get my child vaccinated" or "I'm unsure if I want my child to get vaccinated"

Exclusion Criteria:

  • Cannot read/speak English

Sites / Locations

  • UMHS Outpatient Pediatrics

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tailored information

Untailored information

Arm Description

Individuals assigned to the experimental group will receive individually-tailored educational messages.

Individuals assigned to the control group will receive generic, untailored educational messages.

Outcomes

Primary Outcome Measures

Parent's intention to vaccinate child against MMR
Parent will rate his/her intention to have child vaccinated against MMR using a Likert scale before and after the intervention.

Secondary Outcome Measures

Use of the intervention
We will assess the number of pages viewed and time spend per page for each participant viewing the intervention.

Full Information

First Posted
June 7, 2011
Last Updated
December 8, 2014
Sponsor
University of Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT01369394
Brief Title
Making Decisions About the Measles-Mumps-Rubella Vaccine
Official Title
Developing a Computer-based Intervention That Provides Individually-tailored Educational Information for MMR Vaccine-hesitant Parents
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to determine whether a computer-based intervention that delivers individually-tailored educational messages about the MMR vaccine increases MMR vaccine-hesitant parents' intentions to have their children vaccinated.
Detailed Description
This will be a randomized controlled intervention trial for MMR vaccine-hesitant parents of children ages six years and younger who have not yet received the MMR vaccine. Parents will complete a three-item measure that assesses their baseline intentions for having their children vaccinated with MMR. Participants will then fill out a short, computer-based survey that assesses demographic factors, prior experience with MMR, and views about a variety of potential barriers to MMR vaccination. Following the survey, the intervention group (40 parents) will view a series of tailored educational messages resembling web pages that uses their survey data to address at an individual level their specific concerns about the MMR vaccine. The control group (40 parents) will view a series of generic educational messages resembling web pages that is similar in appearance to the intervention, but contains only untailored information about the vaccine. After navigating through these educational messages, MMR vaccination intention will be reassessed using the same three-item measure as for the baseline assessment of vaccination intention. The vaccine administration records of the children of these parents will be accessed after parents' participation in the study to assess whether the MMR vaccine was provided to the child.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Measles, Mumps, Rubella, MMR Vaccination
Keywords
Measles, Mumps, Rubella, MMR, Prevention, Tailoring, Persuasive communication, Children

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
79 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tailored information
Arm Type
Experimental
Arm Description
Individuals assigned to the experimental group will receive individually-tailored educational messages.
Arm Title
Untailored information
Arm Type
Active Comparator
Arm Description
Individuals assigned to the control group will receive generic, untailored educational messages.
Intervention Type
Other
Intervention Name(s)
Behavioral: Computer-based tailoring system
Intervention Description
Both the intervention and control groups will use a computer-based tailoring system to respond to survey questions. The computer-based tailoring system will generate educational messages based on participants' responses to survey questions. The intervention group will receive tailored educational messages, whereas the control group will receive generic educational messages. The tailored and generic educational messages will be presented as to look like web pages. However, the messages will only exist on the study computer, and will not be linked to any "live" server or website.
Primary Outcome Measure Information:
Title
Parent's intention to vaccinate child against MMR
Description
Parent will rate his/her intention to have child vaccinated against MMR using a Likert scale before and after the intervention.
Time Frame
Date of intervention (one day)
Secondary Outcome Measure Information:
Title
Use of the intervention
Description
We will assess the number of pages viewed and time spend per page for each participant viewing the intervention.
Time Frame
At the time of intervention participation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Parent is greater than or equal to 18 years of age Parent has a child 6 years of age or younger When asked to describe how he/she feels about getting child vaccinated against MMR, parent responds "I don't want to get my child vaccinated" or "I'm unsure if I want my child to get vaccinated" Exclusion Criteria: Cannot read/speak English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amanda Dempsey, MD, PhD, MPH
Organizational Affiliation
Children's Outcomes Research Program
Official's Role
Principal Investigator
Facility Information:
Facility Name
UMHS Outpatient Pediatrics
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Making Decisions About the Measles-Mumps-Rubella Vaccine

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