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Clinical Trials/NCT02097914
NCT02097914
Completed
Not Applicable

Brief Interventions to Create Smoke-Free Home Policies in Low-Income Households: Texas Effectiveness Trial

The University of Texas Health Science Center, Houston1 site in 1 country508 target enrollmentMarch 2014
ConditionsChronic Disease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Disease
Sponsor
The University of Texas Health Science Center, Houston
Enrollment
508
Locations
1
Primary Endpoint
Presence of a total home smoking ban
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The burden of tobacco use falls disproportionately on low-income populations, through high rates of primary smoking and exposure to secondhand smoke. The remarkable progress in creating smoke-free environments in the U.S over the past two decades has left smoker's homes as one of the primary sources of exposure to secondhand smoke for both children and nonsmoking adults. Intervention research that identifies effective and practical strategies for reaching the minority of households that still allow smoking in the home has considerable potential to reduce smoke exposure, but suitable channels to reach low-income families are limited.

The proposed research will systematically test an intervention designed to create smoke-free homes in low income households among 2-1-1 callers. During this randomized control trial, researchers will disseminate and evaluate a brief smoke-free homes intervention through the established infrastructure of a Texas 2-1-1 call center. 2-1-1 is a nationally designated 3-digit telephone exchange, similar to 9-1-1 for emergencies or 4-1-1 for directory assistance, that links callers to community-based health and social services. The main hypothesis to be tested is that a higher proportion of households in the intervention group will establish and maintain a smoke-free home than in the measures-only control group.

Registry
clinicaltrials.gov
Start Date
March 2014
End Date
November 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Patricia Dolan Mullen

Professor - Health Prom & Behavioral Sci - SPH

The University of Texas Health Science Center, Houston

Eligibility Criteria

Inclusion Criteria

  • Must be 18 years of age or older.
  • Must speak and understand English.
  • Must smoke and live with at least one other non-smoking person OR be a non-smoker who lives with a smoker(s).
  • Must not have a total smoking ban in their home.

Exclusion Criteria

  • Participants who are in immediate crisis
  • Participants who are calling to be transferred to the TIERS program
  • Participants who are homeless or facing homelessness

Outcomes

Primary Outcomes

Presence of a total home smoking ban

Time Frame: Change from baseline in reported total home smoking bans at 3-month and 6-month follow-up

Secondary Outcomes

  • Cessation (for smokers)(Change from baseline in cessation (for smokers) at 3-month and 6-month follow-up)
  • Stage of change to quit smoking (for smokers)(Change from baseline in stage of change to quit smoking (for smokers) at 3-month and 6-month follow-up)
  • Weekly secondhand smoke exposure for non-smokers(Change from baseline in reported secondhand smoke exposure for non-smokers at 3-month and 6-month follow-up)
  • Cessation attempts (for smokers)(Change from baseline in reported cessation attempts (for smokers) at 3-month and 6-month follow-up)
  • Number of cigarettes smoked (for smokers)(Change from baseline in reported number of cigarettes smoked (for smokers) at 3-month and 6-month follow-up)

Study Sites (1)

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