Evaluating Modes of Influenza Transmission

NCT01710111 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 127

Last updated 2014-01-15

No results posted yet for this study

Summary

The ways in which influenza is transmitted between people are uncertain; for example, we do not know if large droplets or fine particles (aerosols) matter most; both are produced by coughing and sneezing. This means we cannot say what precautions work best in real life. Improving our understanding is vital to allow the development of guidelines and policies to help reduce the transmission of both pandemic and seasonal flu.

The aim of this study is to explore how influenza is spread, specifically by looking at the importance of spread via small particles (aerosols/droplet nuclei) that are carried in respiratory sprays e.g. produced by coughing and sneezing.

The primary objective of this study is:

To estimate the contribution of aerosols/droplet nuclei to influenza transmission by determining the secondary attack rate (SAR) of influenza in Recipients randomised to a control arm (no intervention - allowing all modes of transmission) compared to Recipients randomised to an intervention arm (face shield and hand hygiene - allowing only transmission by aerosols/droplet nuclei) when both groups of Recipients are exposed to Donor volunteers infected with influenza via intranasal drops.

The hypothesis is that:

The SAR will be lower in Recipients exposed only to aerosols/droplet nuclei (intervention arm) compared to those exposed to all modes of transmission (the control arm): aerosols/droplet nuclei, droplet spray (larger respiratory droplets) and transmission through contact.

Conditions

  • Influenza, Human

Interventions

DEVICE

Intervention Recipients Face Shield

Face shield and repeat hand hygiene measures

Sponsors & Collaborators

  • Retroscreen Virology Ltd.

    collaborator INDUSTRY
  • Wake Forest University Health Sciences

    collaborator OTHER
  • University of Maryland

    collaborator OTHER
  • University of Leeds

    collaborator OTHER
  • Building Services Research and Information Association (BSRIA)

    collaborator UNKNOWN
  • University College, London

    collaborator OTHER
  • Mount Sinai Hospital, New York

    collaborator OTHER
  • Imperial College London

    collaborator OTHER
  • University of Glasgow

    collaborator OTHER
  • Sydney Children's Hospitals Network

    collaborator OTHER
  • University of Nottingham

    lead OTHER

Principal Investigators

  • Jonathan S Nguyen-Van-Tam, BM, BS, DM · University of Nottingham

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-07-31
Completion
2013-07-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01710111 on ClinicalTrials.gov