Smoking Cessation Clinical Trial
Official title:
Building Capacity and Promoting Smoking Cessation in the Community Via "Quit to Win" Contest 2016: a Single-blind Cluster Randomized Controlled Trial on High Intensity Active Referral and Simple Text Messaging to Achieve Abstinence
Verified date | October 2016 |
Source | The University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present study will examine (1) the effectiveness of personalised active referral to smoking cessation (SC) services and text messaging on encouraging SC services (2) explore the use of CBPR model to build capacity and to engage community partners in taking on this important public health issue for sustainability in the community. In addition, process evaluation will be conducted to assess the effectiveness of the recruitment activity and how it is linked with the overall program outcomes.
Status | Completed |
Enrollment | 1200 |
Est. completion date | August 31, 2017 |
Est. primary completion date | April 30, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Hong Kong residents aged 18 or above - Smoke at least 1 cigarette per day in the past 3 months - Able to communicate in Cantonese - Exhaled carbon monoxide (CO) 4 ppm or above, assessed by a validated CO smokerlyzer - Have Intention to quit / reduce smoking Exclusion Criteria: - Smokers who have difficulties (either physical or cognitive condition) to communicate - Currently following other smoking cessation programs |
Country | Name | City | State |
---|---|---|---|
China | The Hong Kong Council on Smoking and Health (COSH) | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong | Hong Kong Council on Smoking and Health (COSH) |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | smoking quit rate change from baseline at 3-month follow-up | The primary outcomes are self-reported 7-day point prevalence (pp) quit rate at 3 month among the three groups | 3-month follow-up | |
Primary | smoking quit rate change from baseline at 6-month follow-up | The primary outcomes are self-reported 7-day point prevalence (pp) quit rate at 3 month among the three groups | 6-month follow-up | |
Secondary | Biochemical validated quit rate | biochemically validated quit rates at 3 month in the three groups | 3-month follow-up | |
Secondary | Biochemical validated quit rate | biochemically validated quit rates at 6 month in the three groups | 6-month follow-up | |
Secondary | Smoking reduction rate change from baseline at 3-month follow-up | rate of smoking reduction by at least half of baseline amount in the three groups | 3-month follow-up | |
Secondary | Smoking reduction rate change from baseline at 6-month follow-up | rate of smoking reduction by at least half of baseline amount in the three groups | 6-month follow-up | |
Secondary | Smoking quit attempt change from baseline at 3-month follow-up | number of quit attempts at 3 month among the three groups | 3-month follow-up | |
Secondary | Smoking quit attempt change from baseline at 6-month follow-up | number of quit attempts at 6 month among the three groups | 6-month follow-up | |
Secondary | quit rate for all subjects change from baseline at 3- and 6-month follow-up | the above cessation and reduction outcomes of all subjects participating in Quit to Win contest 2016 | 3 and 6 months follow-up | |
Secondary | Reduction rate for all subjects change from baseline at 3- and 6-month follow-up | the above cessation and reduction outcomes of all subjects participating in Quit to Win contest 2016 | 3 and 6 months follow-up | |
Secondary | Use of smoking cessation service | use of smoking cessation at 3 and 6 month follow-up among three groups | 3 and 6 months follow-up | |
Secondary | Use of smoking cessation service for all subjects | Use of smoking cessation service for all subjects participating in Quit to Win contest 2016 | 3 and 6 months follow-up |
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