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Clinical Trials/NCT00960596
NCT00960596
Unknown
Not Applicable

Preventive Medicine Study of Childhood Atopic Diseases

National Taiwan University Hospital1 site in 1 country100 target enrollmentJuly 2009
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
National Taiwan University Hospital
Enrollment
100
Locations
1
Primary Endpoint
urine cotinine level
Last Updated
16 years ago

Overview

Brief Summary

Under environmental intervention programs, to explore the associations between Environmental Tobacco Smoke (ETS) and changes of pulmonary function, cytokines and new-onset asthma between different groups.

Detailed Description

Environmental intervention programs: We will both interview by telephone and mail the health education leaflets, in order to achieve the following aims: -Smokers living with the children will change where smoking takes place for reducing the children's ETS exposure. Data collection: We will contact participants individually to get informed consent before data collection. No matter what intervention, non-intervention or reference group, all participants will test as follows: * Blood sample collection: We will test the total IgE, specific IgE, cytokines, such as IL-4, IL-13, TNF-α, ECP and EOS. * Questionnaire collection * Pulmonary function test After intervention programs applied, all participants will test pulmonary function, and total IgE, specific IgE and cytokines by blood sample after six months by school approaches. Then, we can compare the pulmonary function, total IgE, specific IgE and cytokines before and after intervention programs.

Registry
clinicaltrials.gov
Start Date
July 2009
End Date
June 2010
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Only one smokers living in the same household
  • Having smoking exposure during the past 12 months while questionnaire surveying
  • Child without smoking habit

Exclusion Criteria

  • None of above

Outcomes

Primary Outcomes

urine cotinine level

Time Frame: six months, one year

Study Sites (1)

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