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

The University of Hong Kong (HKU)

Status: Active, not recruiting

Conditions: Smoking Cessation

Treatments: Behavioral: Text message; Behavioral: Phone follow-up/counselling service; Behavioral: Personalized chat-based interactions; Behavioral: General health talk; Drug: Mailed nicotine replacement therapy (NRT)

Study type: Interventional

Funder types: Other

Identifiers

NCT04772521

LST SCPW P5

Details and patient eligibility

About

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. Moreover, The COVID-19 pandemic and new normal increase in mental health burden to people in the workplace. An online survey during the pandemic found 88% of Hong Kong employees suffered from stress at work during the past 7 days. Mental health can be both precursors and consequences of smoking. However, the effectiveness of a smoking cessation programme conducted in workplace is yet to be examined in Hong Kong, and the mental health support for smoking employees in promoting smoking cessation is not clear. Thus, this study aims to test, by a 2-arm RCT, the effectiveness of an intervention of which includes mobile phone-based intervention on reducing mental health symptoms and smoking cessation in workplaces in Hong Kong; identify facilitators and barriers of successful policy implementation and quitting; examine and evaluate the company environment and their policies in promoting smoking cessation.

Full description

This study will separate into two phases. Phase I is a large scale cross-sectional survey of corporations in Hong Kong to examine the employers' knowledge, attitudes and practices in promoting SC in the workplace. Phase II is a 2-arm randomized controlled trial that will be conducted to examine the effectiveness of mobile phone-based intervention combined with company health talk, brief phone counselling and nicotine replacement therapy sampling, for SC in workplaces.

Data analyses

Phase I:

Descriptive statistics will be used to analyze the (1) profile of the corporations, including the total number of employees and smoking employees; (2) employers/managerial staff's knowledge on smoking; (3) employers/managerial staff's attitudes on smoking cessation; (4) practices of the companies with respect to smoking cessation.

Phase II:

Primary outcome is self-reported abstinence in the past 7 days at 6-month follow-up. Secondary outcomes for smoking cessation include self-reported abstinence in the past 7 days at 9- and 12-month follow-ups, the biochemically validated abstinence (defined as exhaled CO level <4ppm and saliva cotinine level ≤30 ng/ml); smoking reduction (50% or above reduction in cigarette consumption compared with baseline. Secondary outcomes for mental health include stress (Perceived Stress Scale-10), depression (Personal Health Questionnaire for Depression), anxiety (Generalized Anxiety Disorder scale) and self-rated health.

Descriptive statistics such as frequency, percentage, and mean will be used to summarize the outcomes and other variables. Chi-square tests and t-tests will be used to compare outcome variables between subgroups. The intention-to-treat (ITT) analysis will be used such that those lost to contact and refused cases at the follow-ups will be treated as no reduction in cigarette consumption nor quitting. Multiple imputations will be used to compute missing data for outcome variables. The association between intervention adherence (e.g., engagement in the IM interaction) and the primary outcome within the participants in the intervention group will be examined. The intervention effect by subgroups will be assessed respectively, including sex, age, education level, company types, previous quit attempts, cigarette dependence, and intention to quit, although the statistical power would be lower due to smaller numbers.

Enrollment: 300 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Hong Kong residents aged 18 or above
2. Smoke at least 1 cigarette per day or use e-cigarette (EC) or heated tobacco product (HTP) daily
3. PSS-4 score ≥ 6, or GAD-2 score≥ 3, or PHQ-2 score≥ 3
4. Able to communicate in Cantonese/Mandarin and read Chinese
5. Able to use instant messaging tool (e.g. WhatsApp) for communication.
6. Stay in Hong Kong during the intervention and follow-up periods (12 months)

Exclusion criteria

1. Smokers who are psychologically or physically unable to communicate
2. Currently following other smoking cessation program(s)
3. Smokers who have severe mental illness

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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300 participants in 2 patient groups, including a placebo group

Intervention

Experimental group

Description:

Personalized chat-based support and nicotine replacement therapy sampling (NRT-S) for continued smokers at 6 months for intervention group

Treatment:

Behavioral: Phone follow-up/counselling service

Drug: Mailed nicotine replacement therapy (NRT)

Behavioral: Personalized chat-based interactions

Behavioral: General health talk

Control

Placebo Comparator group

Description:

Regular text-based support and nicotine replacement therapy sampling (NRT-S) for continued smokers at 6 months for control group

Treatment:

Behavioral: Text message

Behavioral: Phone follow-up/counselling service

Drug: Mailed nicotine replacement therapy (NRT)

Behavioral: General health talk