Opting In vs Opting Out

Completed · Not applicable

Conditions studied: Influenza Vaccination

In brief

The purpose of this study is to compare methods for consenting (opting in vs opting out) on influenza vaccine uptake rate in pregnant women. This study is designed to learn about the impact of influenza vaccination in pregnant women. This study will help gather knowledge about influenza vaccine side effects (if given) and whether the vaccine reduces the number of respiratory infection in mothers and their infants.

Key facts

Study ID

NCT01233804

Run by

The University of Texas Health Science Center, Houston

People needed

280

Starts

2010-11-01

Expected to finish

2011-08-01

Last updated by the study team

2018-05-31

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• pregnant female age >17 years
• presenting for routine PNC at UT Houston or UT Galveston
• pregnant during influenza season
• pregnant when influenza vaccine available

You may not qualify if…

• influenza vaccine contraindication

Where it is running

• University of Texas Medical Branch, Women's Clinics — Galveston, Texas, United States
• University of Texas Health Science Center at Houston, Professional Building — Houston, Texas, United States

Full record on ClinicalTrials.gov

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