Effectiveness of Comics to Promote Tobacco-related Knowledge, Attitudes and Behaviours Among Primary School Students

April 28, 2026 updated by: Au Yeung, Shiu Lun Ryan, The University of Hong Kong

A Pilot Randomised Controlled Trial (RCT) on the Effectiveness of Comics to Promote Tobacco-Related Knowledge, Attitudes and Behaviours Among Primary School Students

The goal of this pilot RCT is to evaluate the effectiveness of comics containing tobacco-related content in improving tobacco-related knowledge and attitudes among Hong Kong primary school students. The main questions it aims to answer are:

  • Is the intervention (i.e. comics) effective in improving tobacco-related knowledge (including alternative smoking products (ASPs) and tobacco control development in the world and Hong Kong) compared to controls (i.e. information sheets)?
  • Is the intervention (i.e.comics) effective in improving tobacco-related attitudes and intentions (including ASPs and tobacco control development in the world and Hong Kong) compared to controls (i.e. information sheets)?

Researchers will compare the questionnaire results from students to see if intervention groups (students reading comics) will have better tobacco-related knowledge, higher anti-tobacco attitudes and lower intention to smoke compared to the control group (students reading information sheets).

Study Overview

Status

Active, not recruiting

Conditions

Study Type

Interventional

Enrollment (Estimated)

1000

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Hong Kong, Hong Kong
        • Local primary schools

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Primary 5-6 students from local primary schools
  • Able to read Chinese

Exclusion Criteria:

- None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Intervention group students will receive a series of five tobacco-related comics during the 2-week study period.
A series of five comics are developed specifically for this study. The comics will address five key themes which we found could be reinforced based on our previous project. This includes [1] the harms of tobacco use, [2] secondhand smoke (SHS), [3] thirdhand smoke (THS), [4] alternative smoking products (ASPs), and [5] the tobacco industry and tobacco-related policies in Hong Kong and worldwide.
Active Comparator: Control
Control group students will receive five conventional health leaflets or related educational materials.
The selected leaflets will be based on information from existing tobacco prevention leaflets routinely distributed by the Tobacco and Alcohol Control Office and the Student Health Service and specifically targeting students.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effectiveness of intervention on tobacco-related intentions (including ASPs and tobacco control development in the world and Hong Kong)
Time Frame: Right before the intervention and at 12-16th days.

Students were asked: If one of your good friends offers you a traditional cigarette, e-cigarette or heated tobacco product, ask you to have a few puffs, and no one will know about this as no more smoking in the future. Will you use them?

Students' intention will be assessed using a 5-point Likert scale, with each item rated on a 5-point Likert scale ranging from 1 (Definitely no) to 5 (Definitely yes). Lower scores indicate a lower intention to use ASPs.

Right before the intervention and at 12-16th days.
Effectiveness of intervention on tobacco-related knowledge (including ASPs and tobacco control development in the world and Hong Kong)
Time Frame: Right before the intervention and at 12-16th days

Students reported their opinions towards 5 statements in both pre-test and post-test:

1) Smoking accelerates skin ageing; 2) Secondhand smoke can trigger asthma and middle ear infections in children; 3) Opening windows or using a fan can eliminate the effects of thirdhand smoke; 4) E-cigarettes with added flavors are harmless to the body; 5) Hong Kong prohibits smoking while queuing for public transport.

Questions may be subject to change, as they will be adjusted according to the leaflets/comics, while maintaining a similar format.

Students' knowledge will be assessed using a 3-point Likert scale, with each item rated on a 3-point Likert scale ranging from -1 (wrong) to 1 (correct).

Right before the intervention and at 12-16th days
Effectiveness of intervention on tobacco-related attitudes (including ASPs and tobacco control development in the world and Hong Kong)
Time Frame: Right before the intervention and at 12-16th days.

Students will report their opinions towards 5 statements: 1) Banning smoking in all places would harm smokers' rights; 2) I will actively avoid secondhand smoke; 3) Using e-cigarettes is safer than smoking traditional cigarettes; 4) Tobacco companies use various methods to encourage people to smoke; 5) The government should ban the sale of flavored smoking products.

Questions may be subject to change, as they will be adjusted according to the leaflets/comics, while maintaining a similar format.

Students' attitudes will be assessed using a 5-point Likert scale, with each item rated on a 5-point Likert scale ranging from 1 (Strongly disagree) to 5 (Strongly agree). Item scores will be recoded as appropriate, so that higher scores consistently reflect more negative attitudes.

Right before the intervention and at 12-16th days.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effectiveness of intervention on SHS and THS exposure at home
Time Frame: Right before the intervention and at 12-16th days.

Students were asked: In the past 7 days, how many days (0-7) 1) was someone smoking next to you when you were at home? 2) do you smell secondhand smoke drifting in from outside when you were at home? 3) was someone smoking next to you when you were outside home? 4) you can smell cigarette smoke on objects or people when you are at home and no one is smoking, and you don't see any smoke?

Each item was rated on an 8-point scale ranging from 0 (0 days) to 7 (7 days), with higher scores indicating more frequent exposure to secondhand smoke (i.e., a worse outcome).

Right before the intervention and at 12-16th days.
Effectiveness of intervention on tobacco use
Time Frame: Right before the intervention and at 12-16th days.
Students were asked: 1) Which of the following tobacco products have you ever used? 2) In the past 30 days, which of the following tobacco products have you used?
Right before the intervention and at 12-16th days.
Adherence to the 5-day intervention
Time Frame: At 12-16th days
Students will report their adherence to the intervention. Students were asked: In the past two weeks, how many comics / leaflets did you read in total?
At 12-16th days
Satisfaction of students towards intervention
Time Frame: At 12-16th days

Students were aksed:

  1. Do you find the content of the comics / leaflets engaging?
  2. Do you think the content of the comics / leaflets is easy to understand?
  3. What do you think about the length of the comic/leaflet?
  4. If the comics / leaflets include more new information about tobacco in the future, would you like to read them?
At 12-16th days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Shiu Lun Ryan Au Yeung, School of Public Health, The University of Hong Kong

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 20, 2026

Primary Completion (Estimated)

July 31, 2026

Study Completion (Estimated)

August 31, 2026

Study Registration Dates

First Submitted

February 27, 2026

First Submitted That Met QC Criteria

February 27, 2026

First Posted (Actual)

March 6, 2026

Study Record Updates

Last Update Posted (Actual)

May 4, 2026

Last Update Submitted That Met QC Criteria

April 28, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • coshrct2526

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified individual participant data underlying the results in this article, including text, tables, figures, and appendices, along with the study protocol and statistical analysis plan, will be available for sharing. Data access will be granted starting three months after publication and will remain available for up to five years. Researchers with a methodologically sound proposal aligned with the approved study objectives may request access by contacting the principal investigator(PI) (Ryan Au Yeung) at ayslryan@hku.hk. Approved data requestors will be required to sign a data-access agreement.

IPD Sharing Time Frame

Starting three months after publication and will remain available for up to five years.

IPD Sharing Access Criteria

Researchers with a methodologically sound proposal aligned with the approved study objectives may request access by contacting the PI (Ryan Au Yeung) at ayslryan@hku.hk. Approved data requestors will be required to sign a data-access agreement.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Tobacco Prevention

Clinical Trials on Tobacco-related comics

Subscribe