Smoking Reduction and Cessation Interventions for Chinese

Not Applicable

Completed

• Conditions: Smoking Cessation
• Interventions: Behavioral: Expert System Only; Behavioral: Enhanced Expert System

• Registration Number: NCT00714532
• Lead Sponsor: University of California, San Francisco

Brief Summary

This study aims at developing and testing a stage-based scheduled smoking intervention that targets to encourage smokers to reduce smoking and to facilitate smoking abstinence. We hypothesize that smokers who receive the staged-based scheduled smoking intervention will be more likely to report smoking abstinence, quit attempts, and smoking reduction at 12 months.

Detailed Description

The objective of the study is to document and systematically investigate the use of smoking reduction and cessation strategies targeting Chinese American smokers at various level of readiness to quit smoking.

Using a randomized controlled study design, the experimental intervention will be compared to a control group that will receive the expert system intervention only at 3-, 6- and 12-month follow-up. The primary aim is to test the following hypotheses:

1. Participants receiving the experimental intervention will be more likely to achieve at least a 50% reduction from baseline at 3-month (end of treatment), 6- and 12-month follow-up than participants in the control condition.

2. Participants receiving the experimental intervention will be more likely to report a 24- hour quit attempt at 3-, 6- and 12-month follow-up.

3. Participants receiving the experimental intervention will be report a longer length of abstinence in their quit attempts at 3-, 6- and 12-month follow-up.

4. The experimental condition will yield a higher rate of smoking abstinence at 3-, 6- and 12-month follow-up.

The secondary aim is to examine the feasibility of the proposed intervention which will be assessed by recruitment efficiency, refusal rates, adherence, usage, safety data, and perceived helpfulness of the intervention components. In addition, analyses will be pursued to explore both short- and long-term maintenance of smoking reduction achieved, the association between smoking reduction and changes in self-efficacy of resisting from smoking, stage movements (changes in readiness for quitting), and the use of coping strategies for smoking at follow-ups. The study will provide important empirical data for developing effective smoking cessation strategies that are culturally and linguistically appropriate for the Chinese American population.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2007-04
• Study First Submitted: 2008-07-09
• Study First Submitted QC: 2008-07-09
• Study First Posted: 2008-07-14
• Primary Completion: 2009-06
• Study Completion: 2009-06
• Status Verified: 2013-07
• Last Update Submitted: 2013-07-09
• Last Update Posted: 2013-07-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 298

Inclusion Criteria

• Self-identified ethnic Chinese men and women
• 18 years or older
• report smoking cigarettes daily with at least 5 cigarettes per day in the last 7 days
• reside in California
• be able to read written English or Chinese

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Exclusion Criteria

• Currently engaging in assisted smoking cessation efforts
• Have health conditions that have contraindications of using nicotine replacement treatment (NRT) such as pregnancy, within 6 months post MI, severe or unstable angina

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Expert System Only	Expert system only, which includes a stage-matched manual, and a series of 3 individualized tailored feedback reports at baseline, 1, and 3 months.
2	Enhanced Expert System	The intervention consists of 3 components: * Expert system which includes a stage-matched manual, and a series of 3 individualized tailored feedback reports at baseline, 1, and 3 months * scheduled smoking intervention, which includes a tailored-made 3-week smoking reduction schedule and a stage-matched tip guide to explain why and how to use the smoking reduction intervention * telephone check-in calls to provide brief counseling and technical support to motivate participants to use the intervention materials * a 2-week supply of nicotine gum or lozenge per participants' choice to use during smoking reduction

Primary Outcome Measures

Name	Time	Method
self-report 7-day smoking abstinence	12 months

Secondary Outcome Measures

Name	Time	Method
self-report a 24-hour quit attempt	12 months
50% or more reduction in smoking from baseline	12 months

Trial Locations

Locations (1)

UCSF Langley Porter; 🇺🇸 San Francisco, California, United States