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A Randomized, Controlled, Unblinded, Clinical Trial of the Acceptability and Efficacy of Non-Pharmaceutical Methods in Preventing Spread of Influenza Within the Family
This study is not yet open for participant recruitment.
Verified by Ministry of Health, Israel, December 2006
First Received: December 11, 2006   No Changes Posted
Sponsored by: Ministry of Health, Israel
Information provided by: Ministry of Health, Israel
ClinicalTrials.gov Identifier: NCT00410176
  Purpose

The proposed study will evaluate whether the use of non-pharmaceutical methods, such as surgical masks, isolation of patients and personal hygiene, are acceptable and effective in preventing the spread of influenza within the family.This will be achieved by conducting a randomized, controlled, unblinded, clinical trial. Family members of an index case with influenza like illness, will be randomly allocated to two groups. In the intervention group, family members will receive comprehensive guidance about sanitation and hygiene, as well as surgical masks to wear whenever in close contact (3 feet / 1 meter) with the index case. In addition, they will be asked to isolate the index case as much as possible. In the control group, family members will receive only standard guidance about sanitation and hygiene relevant for reducing the transmission of influenza. The primary end-point of the study will be secondary infection of influenza of at least one of the family members in order to asses the efficacy of the interventions. In addition, the compliance to those interventions will be evaluated. The study hypothesis is that use of non-pharmaceutical methods will be acceptable and will reduce the secondary infection rate among them by 50%.


Condition Intervention
Influenza
Behavioral: sanitation and personal hygiene

MedlinePlus related topics: Flu Germs and Hygiene
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study

Further study details as provided by Ministry of Health, Israel:

Primary Outcome Measures:
  • secondary infection of influenza within the family

Secondary Outcome Measures:
  • compliance of non-pharmaceutical interventions

Estimated Enrollment: 400
Study Start Date: January 2007
  Eligibility

Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Family members of an index case with influenza-like illness (ILI) during the first two days of his illness.
  • No limitations will be given regarding the number of family members.

Exclusion Criteria:

  • Presence of another household member with ILI during the previous two weeks.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00410176

Contacts
Contact: Manfred S Green, PhD, M.D 972-3-7371500 ext 203 m.green@icdc.health.gov.il

Sponsors and Collaborators
Ministry of Health, Israel
Investigators
Principal Investigator: Manfred S Green, PhD, M.D ICDC
  More Information

No publications provided

Study ID Numbers: 4335CTIL
Study First Received: December 11, 2006
Last Updated: December 11, 2006
ClinicalTrials.gov Identifier: NCT00410176     History of Changes
Health Authority: Israel: Ethics Commission;   Israel: Ministry of Health

Study placed in the following topic categories:
Virus Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Influenza, Human
Orthomyxoviridae Infections

Additional relevant MeSH terms:
Virus Diseases
RNA Virus Infections
Respiratory Tract Diseases
Respiratory Tract Infections
Influenza, Human
Orthomyxoviridae Infections

ClinicalTrials.gov processed this record on May 06, 2009