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Clinical Trials/NCT01772901
NCT01772901
Completed
Not Applicable

A Randomized Controlled Trial of a Brief Educational Intervention to Increase Uptake of Influenza Vaccine Among Pregnant Women

The University of Hong Kong4 sites in 1 country321 target enrollmentOctober 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Influenza
Sponsor
The University of Hong Kong
Enrollment
321
Locations
4
Primary Endpoint
The proportion of influenza vaccination
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The investigators will conduct a brief educational intervention to pregnant women who have not yet received the influenza vaccine in this pregnancy to improve the uptake of seasonal influenza vaccine.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
July 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marie Tarrant

Associate Professor

The University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • singleton pregnancy
  • 18 years of age or older
  • in at least the second trimester of pregnancy
  • Cantonese speaking
  • Hong Kong resident
  • no serious medical or obstetrical complications
  • have not yet received the influenza vaccine in this pregnancy
  • staying in Hong Kong for at least two weeks after delivery.

Exclusion Criteria

  • not entitled to health benefits in Hong Kong (NEP)

Outcomes

Primary Outcomes

The proportion of influenza vaccination

Time Frame: 2 weeks postpartum

The proportion of influenza vaccination in the control and intervention groups

Secondary Outcomes

  • the proportion of participants initiating discussion about influenza vaccine with their health care provider(2 weeks postpartum)
  • The influenza and influenza vaccine knowledge of participants(2 weeks postpartum)
  • the proportion of participants seeking out influenza vaccine(2 weeks postpartum)

Study Sites (4)

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