Promoting Home Smoking Restrictions: Biomarker Feedback to Smoking and Non-Smoking Adults

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University of Minnesota - Clinical and Translational Science Institute
ClinicalTrials.gov Identifier:
NCT01497158
First received: December 20, 2011
Last updated: August 21, 2014
Last verified: August 2014

December 20, 2011
August 21, 2014
June 2007
February 2012   (final data collection date for primary outcome measure)
  • Comparison of Self-Reported Home Smoking Restrictions - Active Counseling [ Time Frame: From baseline to week 12 ] [ Designated as safety issue: No ]
    Received self-help brochure and biomarker feedback from urine collected from non-smoking adult in home. Outcome criteria categorized into 3 areas: establishment of a complete ban (defined as no one allowed to smoke anywhere, ever), some restrictions (smoking allowed in some places or some time), and no restrictions (smoking permitted anywhere, no rules).
  • Comparison of Self-Reported Home Smoking Restrictions - Control Group [ Time Frame: From baseline to week 12 ] [ Designated as safety issue: No ]
    Received only self-help brochure on home ETS exposure. Outcome criteria categorized into 3 areas: establishment of a complete ban (defined as no one allowed to smoke anywhere, ever), some restrictions (smoking allowed in some places or some time), and no restrictions (smoking permitted anywhere, no rules).
Same as current
Complete list of historical versions of study NCT01497158 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Promoting Home Smoking Restrictions: Biomarker Feedback to Smoking and Non-Smoking Adults
Promoting Home Smoking Restrictions: Biomarker Feedback to Cohabitating Smoking and Non-Smoking Adults

This study is directed at decreasing home environmental tobacco smoking (ETS) exposure with a novel approach of adoption of home smoking restrictions. This will be done by providing the cohabitating smoker and non-smoker with biomarker feedback documenting exposure to ETS. The intent is to identify an intervention strategy(ies) to reduce ETS exposure.

This is a two-group interventional trial targeting cohabitating smokers and non-smokers. Participants will be randomized to the control condition or biomarker feedback group.

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
  • Smoking Cessation
  • Tobacco Use Disorder
  • Other: Self-help brochure
    Self help brochure given at baseline visit.
  • Other: Biomarker feedback
    Biomarker feedback from urine of adult non-smoker in the home.
  • Active Comparator: Control Group
    Participants who received only self-help brochure regarding environmental tobacco smoking (ETS) exposure in the home.
    Intervention: Other: Self-help brochure
  • Active Comparator: Active Group
    Participants who received self-help brochure regarding environmental tobacco smoking (ETS) exposure in the home and biomarker feedback from the urine of cohabitating adult non-smoker in the home.
    Interventions:
    • Other: Self-help brochure
    • Other: Biomarker feedback
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
122
February 2012
February 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Must be at least 18 years of age
  • Cohabitating Non-Smoker (control) and smoker (active)
  • Smoker must test > 6ppm on carbon dioxide (CO) test and non-smoker < 6ppm
  • General good health
  • Written informed consent
  • Live within Twin Cities 7 county metropolitan area (Minnesota)
  • Plan to live in same home for 6 months and be willing for researchers to come to their home

Exclusion Criteria:

  • Individuals that live in a treatment facility or shelter
  • Individuals endorsing current domestic violence
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01497158
2007NT053
No
University of Minnesota - Clinical and Translational Science Institute
University of Minnesota - Clinical and Translational Science Institute
Not Provided
Principal Investigator: Janet Thomas, M.D. University of Minnesota - Clinical and Translational Science Institute
University of Minnesota - Clinical and Translational Science Institute
August 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP