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Clinical Trials/NCT04079569
NCT04079569
Completed
Not Applicable

Empower Korean Families to End Tobacco Use & Smoking Exposure

University of California, San Francisco1 site in 1 country112 target enrollmentAugust 19, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Smoking Cessation
Sponsor
University of California, San Francisco
Enrollment
112
Locations
1
Primary Endpoint
Abstinence
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The goals of the study are to develop a culturally and linguistically appropriate intervention to promote smoking cessation and reduce secondhand smoke exposure for Korean Americans using a family-based intervention approach targeting Korean Americans ages 18 and above in the greater San Francisco Bay Area, CA, and to evaluate efficacy of the proposed intervention. The study is a randomized control trial targeting a total of 8 lay health workers (LHW) and 48 dyads of a daily smoker and a partner who will attend intervention sessions together. The research question is: Can a family-based lay health worker outreach intervention promote smoking cessation and reduce SHS exposure among Korean Americans?

Registry
clinicaltrials.gov
Start Date
August 19, 2019
End Date
March 31, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • reside in California, United States
  • for the smoker participants, they must have smoked at least 1 cigarette in the past 30 days, and have smoked either at least 1 cigarette and/or used e-cigarettes in the past 7 days, and self-identified as Korean or Korean American
  • for partner participants, they must be willing to attend intervention session together with a smoker participant
  • provide a valid contact telephone number and email address for pre- and post-intervention assessments

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Abstinence

Time Frame: 3 months

Biochemically verified 7-day point prevalence of cigarette abstinence at 3-month post baseline assessment (initiation of intervention)

Secondhand smoke (SHS) exposure of non-smokers

Time Frame: 3 months

Biochemically verified 7-day point prevalence of SHS exposure at 3-month post baseline assessment (initiation of intervention)

Percent attendance

Time Frame: 3-month

Percent of participants who attend at least 3 out of 4 planned contacts

Percentage of participants who rate the intervention as helpful

Time Frame: 3 months

Participants will rate their perception as to whether or not they found the intervention to be helpful at the 3 month assessment

Secondary Outcomes

  • Number of Quit attempts(3 months)

Study Sites (1)

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