Skip to content

Randomized Trial to Reduce Environmental Tobacco Smoke in Children With Asthma

Randomized Trial to Reduce Environmental Tobacco Smoke in Children With Asthma

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00006565
Enrollment
225
Registered
2000-12-01
Start date
2000-09-30
Completion date
2004-04-30
Last updated
2016-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, Lung Diseases

Keywords

asthma, HEPA, ETS

Brief summary

The purpose of this study is to test the effects of reducing indoor environmental tobacco smoke (ETS) on unscheduled asthma visits, asthma symptoms, airway inflammation, and exposure to tobacco smoke measured using air nicotine dosimeters, serum and hair cotinine.

Detailed description

BACKGROUND: Asthma, a disease characterized by increased airway reactivity and inflammation in response to a variety of stimuli, is emerging as the most prevalent and serious environmental health problem among children in the United States. Numerous studies, both prospective and cross-sectional, suggest that exposure to ETS is one of the predominate risk factors for childhood asthma, but this has not been confirmed in a controlled trial. DESIGN NARRATIVE: The randomized, double-blind prospective trial involving 225 children with doctor-diagnosed asthma who are exposed to environmental tobacco smoke tests the efficacy of reducing such exposure on unscheduled asthma visits and asthma symptoms. The intervention consists of placement of 2 high efficiency air filtration with activated carbon, potassium permanganate and zeolite filter insert to reduce exposure to ETS in the experimental homes and inactive (placebo) units in the control group homes. The following hypotheses are tested. (1.0) Children assigned to the ETS reduction group will have a greater than 20 percent reduction in unscheduled asthma visits during one-year follow-up compared with those in the control group. (1.1) Children assigned to the ETS reduction group will have significant improvements in asthma symptoms compared with children in the control group. (1.2) Children assigned to the ETS reduction group will have greater than 10 percent reduction in ETS exposure and exhaled nitric oxide, a measure of airway inflammation during one year of follow-up compared with the control group.

Interventions

Placement of two active HEPA air cleaners in the homes of children

DEVICEPlacebo Filtration Unit

Placement of inactive filtration unit in the homes

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Age 6-12 years at enrollment * Doctor diagnosed asthma by ICD-9 billing codes (from billing records) * Greater than 1 exacerbation(s) in the past year requiring an unscheduled asthma visit * Exposed to the smoke of greater than or equal to 5 cigarettes in and around the house per day * Lived within a 9-county area surrounding the city of Cincinnati

Exclusion criteria

* Already using a HEPA air cleaner * Lacked electricity * Had a coexisting medical problem * Family planned to move in the next year

Design outcomes

Primary

MeasureTime frame
Unscheduled asthma visitsMeasured at 12 months

Secondary

MeasureTime frame
Asthma symptomsMeasured at 12 months
Exhaled nitric oxideMeasured at 12 months
Tobacco smoke exposure, measured using air nicotine dosimeters, serum cotinine and hair cotinineMeasured at 12 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026