Influenza Clinical Trial
Official title:
Tolerability and Measurability of the Efficacy of Non Pharmaceutical Measures to Prevent Seasonal Influenza
With this study the investigators will try to assess the tolerability and measurability of
the efficacy of non pharmaceutical measures to prevent seasonal influenza in individual
households. Households with an identified index case of influenza will be randomised into
one of three intervention arms: 1. group, where the household will receive general
information about transmission of influenza virus and means to prevent it (Controls); 2.
group, which will receive surgical masks and be asked to wear them whenever they are in
close contact with the index case or other persons of the household that became ill during
the observation period; 3. group, which will be given and asked to wear surgical masks as
well as to execute intensified hand hygiene.
In addition to assessing the secondary attack rate as our primary outcome measure, the
investigators will also try to evaluate compliance to those interventions by questionnaires.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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