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NICU Asthma Education and Secondhand Smoke Reduction Study

Not Applicable
Completed
Conditions
Respiratory Illness
Interventions
Behavioral: Secondhand Smoke Reduction and Smoking Cessation Counseling
Behavioral: Asthma Education
Registration Number
NCT00499915
Lead Sponsor
University of Rochester
Brief Summary

Premature infants have a significantly increased risk for developing respiratory illnesses and asthma. Secondhand smoke (SHS) also is clearly associated with increased breathing problems in children, thus exposure to smoke makes it substantially more likely for a premature infant to develop wheezing. The overall goal of this study is to test whether comprehensive asthma education combined with a home-based secondhand smoke reduction program can reduce exposure to smoke and prevent respiratory illness among premature infants. Our hypotheses are:

* More premature infants whose families receive asthma education combined with a SHS reduction intervention will live in smoke-free environments compared to infants receiving only asthma education (control group).

* Caregivers receiving the SHS reduction program will have higher rates of quit attempts and less relapse into smoking compared to caregivers in the control group.

* Infants whose families receive the combined intervention will experience less respiratory illness compared to infants in the control group.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
165
Inclusion Criteria
  • ≤32 weeks gestation
  • Planned discharge to home from the Neonatal Intensive Care Unit
  • Parent or caregiver must consent to the intervention
  • The first sibling discharged, for twins or infants from a multiple birth pregnancy
Exclusion Criteria
  • Inability to speak and understand English
  • No access to a working phone for follow-up surveys (either at the subject's home or an easily accessible alternate home)
  • Family residence outside the greater Rochester area (more than 30 miles away)
  • Children in foster care or other situations in which guardian consent cannot be obtained
  • The child having significant medical conditions, including serious heart disease, cystic fibrosis, or other conditions that could interfere with the assessment of respiratory-related outcome measures

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Secondhand Smoke Reduction and Asthma EducationAsthma EducationParents of children in the experimental group will receive asthma education at NICU discharge as well as a secondhand smoke reduction program.
Secondhand Smoke Reduction and Asthma EducationSecondhand Smoke Reduction and Smoking Cessation CounselingParents of children in the experimental group will receive asthma education at NICU discharge as well as a secondhand smoke reduction program.
Asthma EducationAsthma EducationParents of children in the active comparator group will receive asthma education at NICU discharge.
Primary Outcome Measures
NameTimeMethod
Infants Living in Smoke-free Environments.5 months post baseline

Infants living in homes with a "home smoking ban" rule

Secondary Outcome Measures
NameTimeMethod
Respiratory Morbidity Assessed Through Respiratory Symptoms as Well as Health Care Utilization for Respiratory Illnesses.2, 5, and 7-9 months post baseline

Trial Locations

Locations (1)

University of Rochester

🇺🇸

Rochester, New York, United States

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