Creating Smokefree Living Together for Chinese Household Pairs

This study is currently recruiting participants.
Verified May 2012 by University of California, Davis
Sponsor:
Collaborator:
University of California, San Francisco
Information provided by (Responsible Party):
University of California, Davis
ClinicalTrials.gov Identifier:
NCT01592682
First received: April 26, 2012
Last updated: May 8, 2012
Last verified: May 2012

April 26, 2012
May 8, 2012
April 2012
January 2014   (final data collection date for primary outcome measure)
  • Smoking cessation [ Time Frame: 12 months ] [ Designated as safety issue: No ]
  • Elimination of secondhand smoke exposure [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Nonsmoker
  • Urine NNAL (4-(Methylnitrosamine)-1-(3-pyridyl)-1-butanol) [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Smoker and nonsmoker; NNAL is a tobacco-specific carcinogen
Same as current
Complete list of historical versions of study NCT01592682 on ClinicalTrials.gov Archive Site
  • Cigarette consumption [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Smoker
  • Rule for no smoking in home [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Smoker and nonsmoker
  • Reduction in secondhand smoke exposure [ Time Frame: 12 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Creating Smokefree Living Together for Chinese Household Pairs
"Creating Smokefree Living Together": Smokefree Counseling Intervention for Chinese Smokers and Household Nonsmokers

This is a trial of household pairs of a Chinese smoker and nonsmoker randomized either to a smoke-free educational intervention or self-help control group. The smokefree educational intervention includes group education about smokefree environments and smoking cessation, follow-up phone calls, and tobacco exposure lab reports. The control group is referred to usual care with local in-language smoking cessation classes or quitline, and is otherwise assessment only. The investigators hypothesize that pairs in the intervention group will have higher rates of tobacco cessation and elimination of smoke exposure, compared to the control group.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Prevention
  • Smoking
  • Smoke Exposure
Behavioral: Smokefree counseling
Smokefree counseling intervention involves group education sessions, follow-up phone calls, tobacco exposure lab report. Comparison is usual care with referral to local in-language smoking cessation services including quitline.
  • No Intervention: Usual care
    Household pairs that are assessment only and receive usual care of local in-language smoking cessation resource referral including quitline.
  • Experimental: Smokefree counseling
    Household pairs assigned to smokefree counseling intervention, consisting of group education sessions, tobacco exposure lab report, individual follow-up phone calls.
    Intervention: Behavioral: Smokefree counseling
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
280
June 2014
January 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Self-identified Chinese Americans who primarily speak Chinese
  • Self-identified current smoker men and nonsmoker women
  • Pair lives in same household

Exclusion Criteria:

  • Current smoker women
  • Nonsmoker men
Both
18 Years and older
Yes
Contact: Elisa Tong, MD, MA 9167347005 elisa.tong@ucdmc.ucdavis.edu
Contact: Lei-Chun Fung, MSW, MPH 4153647908 lei_chun_fung@hotmail.com
United States
 
NCT01592682
261778, RSGT-10-114-01-CPPB
No
University of California, Davis
University of California, Davis
University of California, San Francisco
Principal Investigator: Elisa K Tong, MD, MA University of California, Davis
University of California, Davis
May 2012

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