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NCT Number: NCT06451081

Brief Behavioural Economic Intervention for Smoking Cessation

The goal of this clinical trial is to test the effectiveness of brief behavioural economic intervention in promoting smoking cessation among smokers in the community.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Community sites

Hong Kong

Location status: Recruiting

Location contact

Tzu Tsun Luk

CONTACT

About this study

Smoking cessation services are free and effective but underused in Hong Kong. Active referral to smoking cessation services has consistently been found effective in promoting service use and successful quitting as a stand-alone strategy or when combined with other interventions. Participants who received active referral are introduced about the cessation services in Hong Kong and offered connection to the services of their choices. Contacts of participants who agreed to be referred are transferred to the selected cessation providers, who will subsequently contact the participants for further treatment.

The current active referral intervention uses an opt-in approach, where participants are required to actively choose to be connected to the services. By leveraging behavioural economic principles, a simple yet promising strategy to strengthen the active referral intervention is to utilize an "opt-out" approach, where participants are automatically referred to the service unless they actively decline the referral. By making referral to smoking cessation services as the default choice, the investigators aim to increase the uptake of these services and thus improve smoking cessation outcomes. Additionally, mobile messaging informed by behavioural economics principles can serve as nudges to prompt smokers to initiate quitting and utilise cessation services.

The clinical trial aims to test the effectiveness of opt-out referral, with or without behavioural economic-based mobile messaging, compared to opt-in referral, in promoting smoking cessation. The trial will be nested within the 15th "Quit to Win" Smoke-free Community Campaign organised by the Hong Kong Council on Smoking and Health.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hong Kong residents aged 18 years or above
  • Smoke cigarette or heated tobacco product or e-cigarette daily in the past 3 months
  • Exhaled carbon monoxide level ≥4 parts per million or a positive salivary cotinine test
  • Able to communicate in and read Chinese
  • Own a smartphone with a mobile instant messaging app installed

Exclusion criteria

  • Participating in another smoking cessation programme or using any smoking cessation drug or nicotine replacement therapy

Treatment and study plan

Brief cessation advice

Behavioral

Participants will receive brief cessation advice following the AWARD (ask, warn, advise, refer, do-it-again) model:

A: Ask about the tobacco use status; W: Warn about the hazards of tobacco use; A: Advise the smokers to quit; R: Refer the smokers to cessation services; D: Do-it-again

Opt-out active referral

Behavioral

Participants will be automatically referred to a smoking cessation service upon joining the trial, unless they choose to opt out. Contacts of participants will be delivered to a service provider of their choice or based on their living district and preferred treatment modality

Behavioral economic mobile messaging

Behavioral

Participants will receive behavioural economics-informed messages via mobile instant messaging for 3 months

Opt-in active referral

Behavioral

Participants will be offered a referral to a smoking cessation service. Contacts of participants who opt-in will be delivered to a service provider of their choice

Primary outcomes

  1. Biochemically validated tobacco abstinence

    Time frame: 6 months after randomisation

    Verified by an exhaled carbon monoxide level of <4 parts per million and a negative salivary cotinine test

Secondary outcomes

  1. Biochemically validated tobacco abstinence

    Time frame: 3 months after randomisation

    Verified by an exhaled carbon monoxide level of <4 parts per million and a negative salivary cotinine test

  2. Self-reported 7-day point-prevalence tobacco abstinence

    Time frame: 3 months after randomisation

    Tobacco abstinence in the past 7 days

  3. Self-reported 7-day point-prevalence tobacco abstinence

    Time frame: 6 months after randomisation

    Tobacco abstinence in the past 7 days

  4. Self-reported 24-hour quit attempt

    Time frame: 3 months after randomisation

    Tobacco abstinence for at least 24 hours

  5. Self-reported 24-hour quit attempt

    Time frame: 6 months after randomisation

    Tobacco abstinence for at least 24 hours

  6. Self-reported use of smoking cessation service

    Time frame: 3 months after randomisation

    Use of any smoking cessation service during the follow-up period

  7. Self-reported use of smoking cessation service

    Time frame: 6 months after randomisation

    Use of any smoking cessation service during the follow-up period

Other outcomes

  1. Self-reported reduction of tobacco consumption

    Time frame: 3 months after randomisation

    Smoking reduction by at least half of the baseline daily number of cigarettes

  2. Self-reported reduction of tobacco consumption

    Time frame: 6 months after randomisation

    Smoking reduction by at least half of the baseline daily number of cigarettes

Study contacts

Contact information is provided by the study sponsor or research team.

Tzu Tsun Luk, PhD, RN

CONTACT

[email protected]

39177574

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Collaborators

  • Hong Kong Council on Smoking and Health

Registry information

Official study title

Building Capacity and Promoting Smoking Cessation in the Community Via "Quit to Win" Contest 2024: a Randomised Controlled Trial of a Brief Behavioural Economic Intervention

Acronym: QTW2024

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jun 10, 2024
Registry last updated
Jul 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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