Smoking Cessation Programme in Workplaces in Hong Kong (Phase III)

Not Applicable

Completed

• Conditions: Smoking Cessation
• Interventions: Behavioral: Health talk plus intensive social media intervention; Behavioral: Health talk plus less intensive social media intervention

• Registration Number: NCT03142555
• Lead Sponsor: The University of Hong Kong

Brief Summary

Smoking causes cardiovascular and respiratory diseases, cancers and diabetes, and it has been a leading risk factor for death globally. Despite the availability of smoking cessation services locally, most smokers do not use such services. Workplace is one of the most convenient platforms to provide smoking cessation services and over 55% of smokers are employed according to the local population-based survey. However, the effectiveness of a smoking cessation programme conducted in workplace is yet to be examined in Hong Kong, and the attitudes and practices of corporations in promoting smoking cessation are not clear. Thus, this study aims to examine the employers'/managerial staff's knowledge, attitudes and practices in promoting smoking cessation in workplace and evaluate the smoking behaviours of participants before and after attending a smoking cessation intervention.

Detailed Description

This study will separate into two phases. Phase I is a large scale cross-sectional survey to corporations in Hong Kong to examine the employers' knowledge, attitudes and practices in promoting smoking cessation in the workplace. Phase II is a randomized controlled trial study to evaluate the effectiveness of a smoking cessation intervention to assess the subjects' smoking behaviors, knowledge on smoking and satisfaction of the smoking cessation services. The investigators are interested to know if the intervention package including health education,social media and telephone follow-up would trigger higher quit rate or other changes in smoking behaviors. The investigators will also monitor the smoking status of the subjects regularly through telephone follow-ups, understand the company's practices about smoke-free policy as well as evaluate the outcomes of the intervention.

The primary outcome of the study is to measure participated smokers' self-reported 7-day point prevalence quit rate at 26 weeks follow-ups. The secondary outcomes include participated smokers' (i) self-reported reduction rate at 52 weeks follow-ups; (ii) self-reported quit attempt at 26 and 52 weeks follow-ups; (iii) self-reported reduction rate at 26 and 52 weeks follow-ups; (iv) Engagement in social media intervention.

Data of the above outcomes will be collected through telephone interviews (follow-ups) by the investigators. Descriptive statistics will be used to measure the (1) basic info of the participants, including the total number of employees and smoking employees; (2) knowledge on smoking of employers/managerial staff; (3) attitudes on smoking cessation of employers/managerial staff; (4) practices of the corporations with respect to smoking cessation. Logistic regression, linear regression and spearman correlation coefficient will be used to examine the relationships between corporates' policy in smoking cessation and the knowledge and attitudes of employers/ managerial staff. Chi square and t-test will also be used to compare the quit rates between groups and logistic regression will be used to predict quitting. Data will be entered and analyzed using IBM SPSS version 23.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2017-04-24
• Study First Submitted QC: 2017-05-03
• Study First Posted: 2017-05-05
• Study Start: 2017-05-11
• Primary Completion: 2019-06-30
• Study Completion: 2021-06-30
• Status Verified: 2021-09
• Last Update Submitted: 2021-09-20
• Last Update Posted: 2021-09-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 679

Inclusion Criteria

• Hong Kong residents aged 18 or above
• Cantonese speaker
• Smoke at least one cigarette per day in the past 30 days
• Stay in Hong Kong during the intervention and follow-up periods (12 months)

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Exclusion Criteria

• Smokers who are psychologically or physically unable to communicate
• Currently following other smoking cessation programme(s)
• Smokers with diagnosed psychiatric illnesses

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Health talk plus intensive social media intervention	Health talk plus intensive social media intervention	Subjects in this group will receive: 1. General health talk; 2. Phone follow-up/counselling service (15 - 30 minutes); 3. Social media (intensive reminders); 4. Regular personalized what's app interaction ( up to 2 months duration)
Health talk plus less intensive social media intervention	Health talk plus less intensive social media intervention	Subjects in this group will receive: 1. General health talk; 2. Phone follow-up/counselling service (15 - 30 mintues); 3. Social media ( less intensive reminders)

Primary Outcome Measures

Name	Time	Method
Self-reported 7-day point prevalence quit rate	26 weeks	Smokers who did not smoke even a puff in the 7 days preceding the follow-up

Secondary Outcome Measures

Name	Time	Method
Engagement in social media intervention	26 weeks	Self-reported engagement in social media intervention in the two groups
Self-reported 7-day point prevalence quit rate	52 weeks	Smokers who did not smoke even a puff in the 7 days preceding the follow-up
Self-reported reduction rate	26 and 52 weeks	Smokers' who reduced tobacco use (in term of daily cigarette consumption) in the follow-up when comparing with the baseline
Self-reported quit attempt rate	26 and 52 weeks	Smokers' who refrained from smoking for 24 hours in the 7 days preceding the follow-up

Trial Locations

Locations (1)

School of Nursing, The University of Hong Kong; 🇭🇰 Hong Kong, Hong Kong