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CompletedNCT03182790Updated Mar 4, 2019

Promoting Smoking Cessation in the Community Via "Quit to Win" Contest 2017

An interventional study of Instant Messaging IM and Regular messages in Smoking Cessation, sponsored by The University of Hong Kong. Completed at 1 site in Hong Kong. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-03-04.

Sponsored by The University of Hong Kong · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
1,311
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The present study will examine (1) the effectiveness of regular messages and semi-personalized instant messaging with AWARD brief advice and active referral to smoking cessation (SC) services and (2) explore the use of CBPR model to build capacity and to engage community partners in taking on this important public health issue for sustainability in the community. In addition, a process evaluation will be conducted to assess the effectiveness of the recruitment activity and how it is linked with the overall program outcomes.

Read the detailed description

Although smoking prevalence is decreasing in Hong Kong, there are still 641,300 daily smokers (10.5%) and half will be killed by smoking which accounts for over 7,000 deaths per year. Smoking also accounts for a large amount of medical cost, long-term care and productivity loss of US$688 million (0.6% Hong Kong GDP). Smoking is a highly addictive behavior and it is difficult for smokers with strong nicotine dependence to quit without assistance. On the other hand, reaching and helping the many smokers who have no intention to quit is a challenge, because they are unlikely to seek professional help from smoking cessation services.

The Quit and Win programme provides an opportunity to reach and encourage a large group of smokers to make quit attempt and maintain abstinence. The Quit and Win model posits that smokers participating in the contest will have higher motivation to quit with incentives and better social support. Studies have found that such quitting contests or incentive programs appeared to reach a large number of smokers and demonstrated a significantly higher quit rate for the quit and win group than for the control group.

Smoking cessation services in Hong Kong are under-used with most of the adult daily smokers (79.6%) who had never used smoking cessation services. Among these smokers, only 2.4% were willing to use the services. Our previous RCT in previous QTW Contest 2015 evaluated the effects of low-intensity active referral (LAR) vs. very brief general SC advice (VBA) on quitting. LAR included onsite AWARD counselling and collection of smokers' personal contact information for SC services providers to connect with the smokers. Findings at 3-month follow-up of this RCT suggested the LAR intervention resulted in significantly higher self-reported quit rate than VBA in the control group (18.7% vs. 14.0%. P\<0.001). Our RCT in previous QTW Contest 2016 evaluated the effects of a higher intensity and personalized active referral (HAR) vs. low intensity text messaging (SMS) vs. very brief SC advice (VBA; control group) on encouraging smoking cessation (SC) service use and increasing the quit rate. Findings at 6-month follow-up of the QTW 2016 RCT showed that the intervention group with HAR had a significantly higher self-reported quit rate than VBA (the control group) (17.0% vs. 11.2%, P = 0.02). Text messaging group also had significantly higher self-reported quit rate than the control group (17.1 % vs. 11.2%, P = 0.02).

However, these SMS-based RCTs could not provide real-time responses from the counsellors, which might weaken the smokers' intention to quit and lower the intensity of social support. In the present proposal, we hope to enrich the SMS-based intervention by using social media such as WhatsApp or WeChat etc., which can provide an interactive platform and develop a semi-personalized interactive IM system that can tailor for the smokers according to their characteristics, needs and demand.

Therefore, the present study will examine (1) the effectiveness of regular messages and semi-personalized instant messaging with AWARD brief advice and active referral to smoking cessation (SC) services and (2) explore the use of CBPR model to build capacity and to engage community partners in taking on this important public health issue for sustainability in the community. In addition, a process evaluation will be conducted to assess the effectiveness of the recruitment activity and how it is linked with the overall program outcomes.

02

Conditions studied

  • Smoking Cessation

Keywords

  • Smoking Cessation
  • Quit to Win
  • Brief intervention
  • Semi-personalized Instant messaging
  • Incentives
  • AWARD model
  • Smoking Cessation Intervention
  • Regular messages
03

In context

Lead sponsor

The University of Hong Kong is the lead sponsor of 1,262 studies on the registry; 340 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Hong Kong residents aged 18 or above
  • Smoke at least 1 cigarette per day in the past 3 months
  • Able to communicate in Cantonese (including reading Chinese)
  • Exhaled carbon monoxide (CO) 4 ppm or above, assessed by a validated CO Smokerlyzer.
  • Intent to quit / reduce smoking
  • Using a cell phone with instant messaging tool (e.g. WhatsApp, WeChat)
  • Able to use instant messaging tool (e.g. WhatsApp, WeChat) for communication

Exclusion criteria

Exclusion Criteria:

  • Smokers who have communication barrier (either physically or cognitively)
  • Have participation in other smoking cessation programmes or services
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
1,311 participants (actual)

Study arms

  • Experimental
    Group A

    Instant Messaging IM + regular messages +AWARD advice + warning leaflet + referral card

    Behavioral: Instant Messaging IM · Behavioral: Regular messages · Behavioral: AWARD advice · Behavioral: Referral card · Behavioral: COSH booklet · Behavioral: Warning Leaflet

  • Experimental
    Group B

    COSH booklet + general brief advices +Placebo Messages

    Behavioral: Brief advice · Behavioral: COSH booklet · Behavioral: Placebo Messages

Interventions

  • BehavioralInstant Messaging IM

    Smokers can communicate with counsellors in real-time through instant messaging (social media). Our counsellors will trigger the conversation and invite the smokers to response after initial contact. Counsellors will keep contact with the smokers to offer help, positive encouragement, reflections and reminders about SC according to smokers' personal needs and to encourage them to seek SC services. Details of successfully booked SC appointment (e.g. SC services address, contact information, date, appointment number etc.) will be delivered to the smokers using IM. All smokers will receive a reminder-to-attend IM messages 1-3 days before the appointment date.

    Also known as: Instant messaging interaction

  • BehavioralRegular messages

    Regular messages, including: harm of smoking, benefit of smoking cessation, importance of adherence to smoking cessation appointment and encouragement on abstinence will be sent to smokers after initial contact via social media.

    Also known as: Regular messages focusing active referral and encouragement

  • BehavioralAWARD advice

    Ask about smoking history, Warn about the high risk of smoking, Advise to quit as soon as possible, Refer to the smoking cessation services, and Do it again (if the smokers refused to set quit date).

    Also known as: Ask, Warn, Advise, Refer, Do-it-again

  • BehavioralReferral card

    The 3-folded "Smoking Cessation Services" card consists of brief information and highlights of existing smoking cessation services, contact methods, motivation information and strong supporting messages or slogans

    Also known as: Smoking Cessation Service Card

  • BehavioralBrief advice

    Very brief, minimal and general smoking cessation advice

    Also known as: Brief smoking cessation advice

  • BehavioralCOSH booklet

    A general smoking cessation self-help booklet

    Also known as: COSH self-help smoking cessation booklet

  • BehavioralPlacebo Messages

    Placebo messages will be sent via smart phones (e.g. social media) to remind subjects to take follow-up calls before each follow-up time points.

  • BehavioralWarning Leaflet

    The leaflet will include the information about the health risks of smoking.

06

What researchers measure

Primary outcomes

  1. Biochemical validated quit rate at 6-month follow-up

    Biochemically validated quit rates at 6-month in the two groups

    Time frame: 6-month follow-up

Secondary outcomes

  1. Biochemical validated quit rate

    Biochemically validated quit rates at 3-month in the two groups

    Time frame: 3-month follow-up

  2. Smoking quit rate change from baseline at 3-month follow-up

    The primary outcomes are self-reported 7-day point prevalence (pp) quit rate at 3-month between the two groups

    Time frame: 3-month follow-up

  3. Smoking quit rate change from baseline at 6-month follow-up

    The primary outcomes are self-reported 7-day point prevalence (pp) quit rate at 6-month between the two groups

    Time frame: 6-month follow-up

  4. Smoking reduction rate change from baseline at 3-month follow-up

    Rate of smoking reduction by at least half of baseline amount in the two groups

    Time frame: 3-month follow-up

  5. Smoking reduction rate change from baseline at 6-month follow-up

    Rate of smoking reduction by at least half of baseline amount in the two groups

    Time frame: 6-month follow-up

  6. Smoking quit attempt change from baseline at 3-month follow-up

    Number of quit attempts at 3-month in the two groups

    Time frame: 3-month follow-up

  7. Smoking quit attempt change from baseline at 6-month follow-up

    Number of quit attempts at 6-month in the two groups

    Time frame: 6-month follow-up

  8. Quit rate for all subjects change from baseline at 3- and 6-month follow-up

    the above cessation and reduction outcomes of all subjects participating in Quit to Win contest 2017

    Time frame: 3 and 6 months follow-up

  9. Reduction rate for all subjects change from baseline at 3- and 6-month follow-up

    the above cessation and reduction outcomes of all subjects participating in Quit to Win contest 2017

    Time frame: 3 and 6 months follow-up

  10. Use of smoking cessation service

    Use of smoking cessation at 3 and 6 month follow-up in the two groups

    Time frame: 3 and 6 months follow-up

  11. Use of smoking cessation service for all subjects

    Use of smoking cessation service for all subjects participating in Quit to Win contest 2017

    Time frame: 3 and 6 months follow-up

07

Study locations

1 site
  • Hong Kong Council on Smoking and Health (COSH)
    Hong Kong, 852, Hong Kong
08

References and documents

Publications

  • Wang MP, Luk TT, Wu Y, Li WH, Cheung DY, Kwong AC, Lai V, Chan SS, Lam TH. Chat-based instant messaging support integrated with brief interventions for smoking cessation: a community-based, pragmatic, cluster-randomised controlled trial. Lancet Digit Health. 2019 Aug;1(4):e183-e192. doi: 10.1016/S2589-7500(19)30082-2. Epub 2019 Jul 31. PubMed 33323188 ↗

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03182790
Lead sponsor
The University of Hong Kong
Collaborators
Hong Kong Council on Smoking and Health
Responsible party
Dr. Wang Man-Ping (Assistant Professor, The University of Hong Kong) — Principal investigator
First posted
Jun 9, 2017
Start date
Jun 18, 2017
Primary completion
Jun 30, 2018
Completion
Sep 30, 2018
Last update
Mar 4, 2019

Study contacts

Man Ping Kelvin Wang, PhD
principal investigator · The University of Hong Kong

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

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