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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02179424
Other study ID # LSTWPLACE
Secondary ID
Status Recruiting
Phase N/A
First received June 27, 2014
Last updated January 19, 2016
Start date December 2012
Est. completion date March 2017

Study information

Verified date January 2016
Source The University of Hong Kong
Contact Tai Hing Lam, MD
Phone +852 2819 9287
Email hrmrlth@hku.hk
Is FDA regulated No
Health authority Hong Kong: Department of HealthHong Kong: Ethics Committee
Study type Interventional

Clinical Trial Summary

Previous research shows a significant proportion of smokers work in full-time employment. Given that the majority of smokers do not aware of the smoking cessation services available in Hong Kong, implementing smoking cessation policy in the workplaces may assist a considerable number of smokers to stop or reduce smoking.

This study aims to:

1. examine the employers' knowledge, attitudes and practices in promoting smoking cessation in workplace.

2. test the effectiveness of a brief and an intensive smoking cessation interventions to help workers stop smoking

In Phase I of this study, a large scale cross-sectional survey will be conducted to 3000 corporate companies in Hong Kong. The questionnaire will examine the employers' knowledge, attitudes and practices in promoting smoking cessation in the workplaces.

In Phase II, a longitudinal study will be conducted to evaluate the effectiveness of a smoking cessation intervention offered by the Department of Psychology, the University of Hong Kong. Smokers from the participating companies will be interviewed before the intervention at baseline, immediately after the intervention, and at 1-, 4-, 12-, 26- and 52-week post-intervention follow-ups.

The follow-up assessments will consist of a biochemical validation for the self-reported quitters who report quitting in the past 7 days via exhaled carbon monoxide and saliva cotinine concentration tests. Participants' smoking behaviour, knowledge on smoking and satisfaction of the smoking cessation services will also be evaluated.

It is hypothesized that the smoking cessation intervention helps workers stop smoking. Employers' knowledge and attitudes are positively associated with the practices in promoting smoking cessation in workplace.

Process evaluation: Qualitative interviews, including in-depth interviews and/or focus group will be conducted after 6-month follow-up.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date March 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Hong Kong residents aged 18 or above

- Cantonese speaker and able to read in Chinese characters

- Smoke at least one cigarette per day

- Stay at Hong Kong during the intervention and follow-up periods (12 months)

Exclusion Criteria:

- Smokers who are psychologically or physically unable to communicate

- Smokers who are currently following other smoking cessation programme(s)

- Smokers with diagnosed psychiatric illnesses

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
Motivational intervention
Use motivational interview strategies to provide smoking cessation intervention

Locations

Country Name City State
China 2/F, 61 Lung Kong Rd, Kowloon City, Lok Sin Tong Benevolent Society Hong Kong

Sponsors (2)

Lead Sponsor Collaborator
The University of Hong Kong The Lok Sin Tong Benevolent Society Kowloon

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes of employers' KAP Employers' knowledge, attitudes and practices (KAP) in promoting smoking cessation in the workplace 1 year No
Primary smoking quit rate quit smoking rate as defined by the self-reported 7-day point prevalence abstinence 6 month follow-up and 12 month follow-up No
Secondary smoking reduction Reduced at least 50% of cigarette consumption 6 month follow-up and 12 month follow-up No
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