- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03182764
Tobacco Control-Related Policy Survey
Policy-Related Survey - Territory-wide Telephone Survey on Tobacco Control
Aim: to collect further information on issues related to tobacco control which should be addressed and advocated in further tobacco control measures in Hong Kong
The objectives of this policy-related survey are as follows:
- to update information on trends and prevalence of secondhand smoke, smoking attributable health effects, cessation services, and e-cigarette;
- to investigate the level of public support on current and future tobacco control measures and taxation;
- to address the timely impacts of smoke-free policies, public support for further tobacco control measures and assist COSH in shaping policy direction for government.
Current study is a cross-sectional retrospective telephone survey based on questionnaires. In total, 5,104 subjects will be randomly selected for a telephone interview. The subjects will be categorized into three groups, i.e. never smokers (1,700), ex-smokers (1,700) and current smokers (1,704). They will be required to answer a questionnaire via telephone. All data shall be collected using a Computer Assisted Telephone Interview (CATI) system, which allows real-time data capture and consolidation. All interviews shall be conducted anonymously. Analysis of survey data will aim to identify current opinion on tobacco control policies and implications for future policies. Analyses will be controlled for confounding variables as required by stratification into sub-groups based on important pre-defined characteristics and/or by multivariate analysis. Comparison with past trends and, where possible, extrapolation of future trends will be explored. Weights will be applied to adjust for the sex and age of Hong Kong population, and to handle the over-sampling issues of current smokers. The data analysis will be conducted by statisticians.
Study Overview
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
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Hong Kong, Hong Kong
- Recruiting
- Public Opinion Programme, the University of Hong Kong
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Contact:
- Joyce Chan
- Phone Number: +852 39177700
- Email: joyce.chan@hkupop.hku.hk
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged 15 or above
- Cantonese or Mandarin speakers
Exclusion Criteria:
- Unable to provide a consent form
- Speak language other than Cantonese and Mandarin
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
never smokers
Never smokers are those who have never consumed cigarettes in their lifetime.
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No intervention
|
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Ex-smokers
Ex-smokers are those who consumed cigarettes previously but do not smoke at the time of the survey.
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No intervention
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Current smokers
Current smokers are those who, at the time of the survey, consume cigarettes daily or occasionally.
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No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attitudes towards tobacco control policies
Time Frame: Finish all telephone survey by Sep 2017
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Topics included the awareness, use and perception of e-cigarettes, and public support for future tobacco control policies such as enlargement of graphic health warnings on cigarette packaging, tobacco tax increase and endgame.
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Finish all telephone survey by Sep 2017
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2017 Policy Survey
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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