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NCT03053674 Clinical Trial

Impact of Explanation Given to Parents on Rate of Post-partum Influenza Vaccination

Newborn Morbidity Clinical Trial

Official title:
Impact of Explanation Given to Parents on Rate of Post-partum Influenza Vaccination

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03053674
Other study ID # HYMC104-16
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 13, 2017
Last updated February 13, 2017
Start date February 20, 2017
Est. completion date July 1, 2017

Study information
Verified date February 2017
Source Hillel Yaffe Medical Center
Contact Amit Hochberg, MD
Email amith@hy.health.gov.il
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine whether an explanation to parents for the need for post-partum influenza vaccination will influence their compliance.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 208
Est. completion date July 1, 2017
Est. primary completion date April 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- All parents discharged from well-baby nursery

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Oral and written explanation
Oral and written explanation on importance of post-partum influenza vaccination for the health of their newborn infant
• Follow-up questionnaire
Follow-up questionnaire to determine whether participants have receive post-partum vaccination

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of post-partum influenza vaccination Telephone questionnaire to parents to determine compliance with vaccination 2 months
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