Promoting Smoking Cessation in the Community Via Quit to Win Contest 2012

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Prof. Sophia Siu-chee Chan, The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT01670864
First received: August 17, 2012
Last updated: July 22, 2013
Last verified: July 2013
  Purpose

Background According to the report of Census & Statistics Department, there are still 659,300 daily smokers (11.1%) in Hong Kong and smoking kills over 7,000 people per year. The Quit and Win programme provided another opportunity to reach large group of smokers, and it aims to widespread quit attempts among smokers via incentives in order to boost up the number of quitters. Although such competitions appear to reach large cohorts of smokers, there is still insufficient evidence of its effectiveness in helping smokers to achieve complete cessation.

Aim This project aims to promote and evaluate community-based smoking cessation services through the Quit to Win Contest organised in the 18 districts of Hong Kong. The specific objectives of the study are (1) to build capacity in the community on smoking cessation through a training programme; (2) to empower the participated NGOs (a) to raise the awareness of smoking cessation in the community level; (b) to reach as many smokers as possible; (c) to arouse the interest of smokers to quit, through organizing the Quit to Win Contest; (3) to test the effectiveness of community-based on-site face-to-face counselling and Short Message Service (SMS) message vs. self-help booklet to assist current smokers to quit smoking; and (4) to build-up a community-based participatory research (CBPR) model in smoking cessation intervention at a district level in Hong Kong.

Methods A community-based participatory (CBP) approach, which is an effective way to engage public health researchers and community members (NGOs, other major stakeholders, and participants), will be used. Two domains of outcome will be assessed: (1) Effectiveness of smoking cessation interventions, (2) process evaluation of the recruitment activities including number of eligible participants and amount of publicity.

Procedure At the recruitment sites, after screening for eligibility of participants for the Quit to Win Contest, smoking counselor will measure eligible participant's level of carbon monoxide (CO) on expired air, and provide the self-help smoking cessation materials developed by the Hong Kong Council on Smoking and Health (COSH). Then the counselor will explain and invite the participants to join the cluster randomized controlled trial on smoking cessation intervention. Participants will be allocated to one of the groups of the smoking cessation intervention. 3- and 6-month follow-ups will be conducted

Hypothesis We hypothesize that the on-site brief smoking cessation advice will lead to significant increases in rates of smoking cessation in the intervention group than the control group (with the self-help materials only). Another hypothesis to be tested is that the intervention of sending SMS messages of smoking cessation advice is effective to increase the quit rate comparing to the control group.


Condition Intervention
Comparative Effectiveness Research
Community-Based Participatory Research
Behavioral: Counseling group
Behavioral: SMS intervention group

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Promoting Smoking Cessation in the Community Via Quit to Win Contest 2012: Aa Cluster Randomized Controlled Trial of 18 Districts in Hong Kong

Resource links provided by NLM:


Further study details as provided by The University of Hong Kong:

Primary Outcome Measures:
  • The self-reported 7-day point prevalence (pp) quit rate of smoking at 3 months [ Time Frame: Three months ] [ Designated as safety issue: No ]
    Whether the participant has quitted smoking in the past seven days at the time point of 3 months


Secondary Outcome Measures:
  • Biochemical validated and self-reported smoking habit at 3 and 6 months [ Time Frame: 3 and 6 months after recruitment ] [ Designated as safety issue: No ]
    • Test the cotinine level in the saliva provided by the participants
    • Self-reported quit rate at 6 months
    • Rate of smoking reduction by at least of half
    • Number of quit attempts at 3 and 6 months

  • Service output of the community-based smoking cessation intervention [ Time Frame: Whole project ] [ Designated as safety issue: No ]
    Assessed by a Process Evaluation onsite observation form, and a series of checklists including participants record list, proposal and final report from NGOs. The components of process evaluation, including context, reach, dose delivered, dose received, fidelity and recruitment will be assessed.


Enrollment: 1193
Study Start Date: July 2012
Study Completion Date: September 2012
Primary Completion Date: September 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Counseling group
Study participants in the counseling group will receive a brief on-site face-to-face smoking cessation counseling from our trained smoking cessation counselor on the study site after signing the consent form. They will receive advice on quitting smoking and specific warning about the hazardous effects of smoking on health. A special designed health education card, based on the health education model, will be also provided to the participants. Additional telephone follow-up counseling (reminder) at 1-week & 1-month will be made to the participants in this group.
Behavioral: Counseling group
The content for the brief counseling group adopts a AWARD approach including asking the smoking habit, warning about the health risks associated with smoking, advising the smokers to quit, referring to specialized service, and repeating the above messages. A special designed health education card, based on the health education model, will be also provided to the participants. Additional telephone follow-up counseling (reminder) at 1-week & 1-month will be made to the participants in this group.
Experimental: SMS intervention group
Study participants in the SMS group will receive SMS text messages on smoking cessation advice and warning on the hazardous effects of smoking on health. The participants will receive a total of 16 tailored SMS messages after recruitment.
Behavioral: SMS intervention group
The text messages are divided into two groups which target to smokers who are ready to quit and those who are not ready to quit. For smokers who are ready to quit, messages would be focused on practical advice and emotional support. For smokers who are not ready to quit, messages would be focused on motivating the smokers to have quit attempt.
No Intervention: Control group
Study participants in the control group will not receive any quitting assistance other than the self-help materials from the recruitment sites.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

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 and read Chinese
  • Have a local network mobile phone
  • Exhaled carbon monoxide (CO) 4 ppm or above, assessed by a validated CO smokerlyzer

Exclusion Criteria:

  • Smokers who have difficulties (either physical or cognitive condition) to communicate
  • Currently following other forms of smoking cessation programme
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01670864

Locations
China
The University of Hong Kong
Hong Kong SAR, China
Sponsors and Collaborators
The University of Hong Kong
  More Information

No publications provided

Responsible Party: Prof. Sophia Siu-chee Chan, Professor, The University of Hong Kong
ClinicalTrials.gov Identifier: NCT01670864     History of Changes
Other Study ID Numbers: QTW2012
Study First Received: August 17, 2012
Last Updated: July 22, 2013
Health Authority: Hong Kong: Ethics Committee

ClinicalTrials.gov processed this record on April 22, 2014