Real-time Influenza Vaccine Surveillance

Completed

Conditions studied: Vaccine Safety

In brief

The aim of this proposal is to pioneer the implementation and evaluation of a novel patient centered text messaging vaccine adverse event surveillance network.

Key facts

Study ID

NCT01233388

Run by

Columbia University

People needed

400

Starts

2010-11-01

Expected to finish

2012-05-01

Last updated by the study team

2012-06-12

Who can join

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

You may qualify if…

• Have an active cell phone with text messaging capability
• Presents for care at participating sites
• Fluent in English or Spanish

Where it is running

• Columbia University Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.