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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02968199
Other study ID # Smoking_1
Secondary ID
Status Completed
Phase N/A
First received November 16, 2016
Last updated March 28, 2017
Start date January 2006
Est. completion date February 2014

Study information

Verified date March 2017
Source The University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study describes the development of a community-based network to promote smoking cessation among female smokers in Hong Kong.


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.


Recruitment information / eligibility

Status Completed
Enrollment 457
Est. completion date February 2014
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
A brief intervention
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.

Locations

Country Name City State
China The University of Hong Kong Hong Kong SAR

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary self-reported 7-day point prevalence of abstinence 6 months
Secondary self-reported reduction of = 50% in cigarette consumption 6 months
Secondary Levels of self-efficacy at baseline baseline
Secondary Levels of self-efficacy at six months six months
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