NCT01772901
Completed
Not Applicable
A Randomized Controlled Trial of a Brief Educational Intervention to Increase Uptake of Influenza Vaccine Among Pregnant Women
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.
Investigators
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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