- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02968199
Building a Community-based Network to Promote Smoking Cessation
March 28, 2017 updated by: The University of Hong Kong
Development of a Community-based Network to Promote Smoking Cessation Among Female Smokers in Hong Kong
This study describes the development of a community-based network to promote smoking cessation among female smokers in Hong Kong.
Study Overview
Detailed Description
There is growing concern about the use of tobacco among women in Hong Kong.
Nevertheless, nearly all of them reported that they had not attended smoking cessation services provided by the government and other organizations, of which only 6.7% indicated that they would like to attend, demonstrating the need for population-based smoking cessation interventions targeting female smokers in Hong Kong.
In response to the increased number of female smokers and their low usage rates of smoking cessation services, the first smoking cessation hotline for female smokers in Hong Kong was established in 2006 by the University of Hong Kong.
The aim of this study was to describe the development of a community-based network to promote the smoking cessation hotline among female smokers in Hong Kong.
Study Type
Interventional
Enrollment (Actual)
457
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Hong Kong SAR, China
- The University of Hong Kong
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Female Hong Kong Chinese current smokers
- Aged 15 years or above
- Able to speak and understand Cantonese
- Willing to receive face-to-face or telephone counseling
Exclusion Criteria:
- Those who were participating in other smoking cessation programs or services
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Referred women
A brief intervention based on the'5 A' model developed by the Agency for Health Care Policy and Research in the United States.
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The content of the intervention includes: (1) asking about tobacco use; (2) advising cessation; (3) assessing willingness to quit; (4) assisting in the attempt to quit; and (5) arranging follow-up.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
self-reported 7-day point prevalence of abstinence
Time Frame: 6 months
|
6 months
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
self-reported reduction of ≥ 50% in cigarette consumption
Time Frame: 6 months
|
6 months
|
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Levels of self-efficacy at baseline
Time Frame: baseline
|
baseline
|
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Levels of self-efficacy at six months
Time Frame: six months
|
six months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: William, Ho Cheung LI, PhD, The University of Hong Kong
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2006
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
February 1, 2014
Study Registration Dates
First Submitted
November 16, 2016
First Submitted That Met QC Criteria
November 16, 2016
First Posted (Estimate)
November 18, 2016
Study Record Updates
Last Update Posted (Actual)
March 30, 2017
Last Update Submitted That Met QC Criteria
March 28, 2017
Last Verified
March 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- Smoking_1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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