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NCT02907580 Clinical Trial

Influenza Vaccine Attitudes, Intent, and Receipt: Pediatric

Influenza Clinical Trial

Official title:
Influenza Vaccine Attitudes, Intent, and Receipt

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02907580
Other study ID # AAAQ9636
Secondary ID
Status Completed
Phase N/A
First received September 8, 2016
Last updated July 26, 2017
Start date September 13, 2016
Est. completion date June 1, 2017

Study information
Verified date July 2017
Source Columbia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Influenza vaccine is recommended as routine care for all individuals who are at least 6 months of age and older. Recently, questions about vaccine safety and concerns for side effects have increased, contributing to both influenza vaccine hesitancy and refusal. In an effort to educate parents and patients, public health entities and physicians give informational handouts in various forms. However, recent publications have found that pro-vaccine messages can have paradoxical effects on vaccine intentions, therefore further studies on vaccine related public health communication is needed. Few, if any, studies have analyzed the relationship between influenza vaccine attitudes and intention with actual vaccine receipt in the pediatric population. These results will help to understand the relationship between parent's vaccine perception and the intent to vaccinate versus the child's receipt of the influenza vaccine, as well as to optimize educational information given to families regarding the influenza vaccine.

Recruitment information / eligibility
Status Completed
Enrollment 400
Est. completion date June 1, 2017
Est. primary completion date May 31, 2017
Accepts healthy volunteers No
Gender All
Age group 6 Months and older
Eligibility Inclusion Criteria:

- Age at least 6 months

Exclusion Criteria:

- Receipt of influenza vaccination that season

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Local educational information
Participants in this arm receive educational information regarding influenza vaccination based on local educational information.
• National educational information
Participants in this arm receive educational information regarding influenza vaccination based on national educational information.

Locations
Country Name City State
United States Columbia University Medical Center New York New York

Sponsors (1)
Lead Sponsor Collaborator
Columbia University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of children who receive influenza vaccination on day of intervention Receipt of influenza vaccination by the child on the day of the educational intervention Day 0
Secondary Number of children who receive influenza vaccination during the influenza vaccine season Receipt of influenza vaccination by the child by April 2017 Up to 7 months
Secondary Number of parents who anticipate influenza vaccination during the influenza vaccine season Parents report planned receipt of influenza vaccination by themselves by April 2017 Up to 7 months
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