Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07049757

Healthy Family Project: Ending Tobacco Use and Smoke Exposure in Asian American Communities

Led by University of California, San Francisco · Updated on 2026-06-04

760

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

U

University of California, San Francisco

Lead Sponsor

T

Tobacco Related Disease Research Program

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the Smokefree Family Living (SFL) intervention to see if it helps Chinese American smokers quit smoking and reduces exposure to third-hand smoke (THS) among smokers and their non-smoking household members. THS refers to tobacco contamination that remains on surfaces like carpets, walls, and furniture even after smoke clears. The study focuses on Chinese American males, particularly those with limited English skills, who have high smoking rates. The SFL program combines smoking cessation education with THS awareness and cleaning strategies. The study includes a family-based intervention development phase followed by a randomized clinical trial with 320 smoker-household member pairs from Chinese American communities. Participants are assigned to one of two groups: one group receives two educational sessions focused on quitting smoking plus THS education and cleaning strategies after six months; the other group receives the same educational sessions but with THS education and cleaning strategies included during the second session. Both groups receive follow-up phone calls, a Healthy Family Action Plan, smoking cessation resources, and urine sample collections. Non-smoking household members wear silicone wristbands for two days at each assessment to measure THS exposure. Participants attend educational sessions and follow-up calls, provide urine samples throughout the study, and non-smoking members wear wristbands to track exposure. Researchers measure smoking quit rates at six months as the primary outcome and assess tobacco smoke biomarker changes and quit rates at twelve months. The study also explores individual and social factors influencing cessation, the timing and long-term effects of the THS intervention, and the feasibility of wristbands for exposure measurement. Participants are followed for up to 12 months with assessments at six and twelve months after intervention completion.

CONDITIONS

Brief Title

Healthy Family Project: Tobacco Use and Smoke Exposure in Asian American Communities

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be 18 years of age or older
  • Must self-identify as Chinese or of Chinese descent
  • Must be able to understand spoken Chinese (Cantonese and/or Mandarin) or English
  • Able to attend educational sessions in person or via video conferencing
  • Willing and able to sign a written informed consent document
  • Have a mobile phone that can receive text messages or an email and phone number for contact
  • Lay Health Workers must have community outreach experience and language proficiency to deliver materials
  • Lay Health Workers must be affiliated with the Chinese Community Health Resource Center or recruited through community networks
  • Smokers must have smoked within the past 30 days, either daily or occasionally
  • Smokers must have a non-smoking household member
  • Family participants must live in the same household as the smoker
  • Family participants must not have used tobacco products in the past 30 days
  • Post-Trial Household Member Group Interview Participants must live with the smoker-household member dyad
Not Eligible

You will not qualify if you...

  • Currently participating in another smoking cessation program
  • Non-resident of California
  • Unwilling to provide follow-up contact for assessments at 6 and 12 months
  • Lay Health Workers unwilling or unable to complete required training or intervention delivery
  • Lay Health Workers unable to maintain confidentiality and professionalism
  • Active participation in conflicting research studies or programs by Lay Health Workers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Educational Sessions and Follow-up Calls

Duration - 6 weeks

Participants attend two Quit Smoking for a Healthy Family educational sessions about 45-60 minutes each one month apart, and receive two follow-up phone calls about 15-30 minutes each 1-2 weeks after each session over 6 weeks. Participants also receive a Healthy Family Action Plan, a smoking cessation resource guide, and set goals on study.

2 educational sessions (in-person or video conferencing) and 2 follow-up phone calls

Third-Hand Smoke Education and Cleaning Intervention

Duration - Up to 6 months

Participants receive third-hand smoke education and cleaning strategies either during the second educational session or at 6 months after the initial sessions depending on study arm.

1 visit for third-hand smoke education and cleaning strategies

Urine Sample Collection and Silicone Wristband Wear

Duration - Up to 12 months

Participants undergo urine sample collection at baseline and throughout the study. Non-smoking household members wear a silicone wristband for 2 days at each assessment to measure third-hand smoke exposure.

Urine samples collected at multiple assessments; silicone wristband worn for 2 days at each assessment by non-smokers

Follow-up Assessments

Duration - 6 to 12 months post-intervention

Participants are followed up at 6 and 12 months after completion of the intervention to assess smoking cessation and exposure to tobacco smoke.

2 follow-up visits at 6 and 12 months

Trial Site Locations

Total: 1 location

1

University of California, San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

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Research Team

E

Edgar Yu

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

PREVENTION

Number of Arms

3

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