- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06812962
A Pilot RCT on the Feasibility of an Online Quiz Game to Promote Tobacco-related Knowledge, Attitudes and Behaviours Among Primary School Students
The goal of this pilot RCT is to test the feasibility of an online quiz game to promote tobacco-related knowledge, attitudes and behaviours in local primary 5-6 school students. The main question it aims to answer is:
- Feasibility of intervention
- Acceptance of intervention by schools, teachers, parents and teachers
- Adherence to the 4-week intervention
- Functional online quiz platform
- Satisfaction of students and parents towards intervention Researchers will compare the questionnaire results from students to see if students doing tobacco-related questions on the online quiz platform will have better tobacco-related knowledge, higher anti-tobacco attitudes and lower intention to smoke.
Students will engage in an online quiz competition for 4 weeks on tobacco-related topics for the intervention group and on healthy eating for the control group. They will complete pre-test and post-test questionnaires before and after the online quiz competition.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Hong Kong, Hong Kong
- Local primary schools
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Primary 5-6 students from local primary schools
- Able to read and communicate in Chinese
- Have a digital device for online access to the quiz game at home
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
Students will engage in an online quiz competition for 4 weeks on tobacco-related topics.
Each day, students could answer a maximum of 5 questions.
|
The intervention and control students participated in an online quiz game on tobacco and healthy eating topics, respectively.
Each day, students could answer a maximum of 5 questions randomly selected from the respective pool of questions by the platform.
The students logged onto the online platform and played the quiz competition on weekdays for 4 weeks (i.e. total of 20 days).
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|
Active Comparator: Control
Students will engage in an online quiz competition for 4 weeks on healthy eating-related topics.
Each day, students could answer a maximum of 5 questions.
|
The intervention and control students participated in an online quiz game on tobacco and healthy eating topics, respectively.
Each day, students could answer a maximum of 5 questions randomly selected from the respective pool of questions by the platform.
The students logged onto the online platform and played the quiz competition on weekdays for 4 weeks (i.e. total of 20 days).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of intervention
Time Frame: During the post-questionnaire at 5th-6th weeks and during the phone interview at 10th-16th weeks.
|
Students and parents will be asked their comments towards intervention in the phone interview: [Students] 1) Did you find the quiz platform interesting or engaging? Why? 2) On a scale of 0 to 10, how much did you enjoy using the quiz platform? [Parents] 1) Do you think using a quiz competition format increases your child's motivation to learn? 2) Are there specific features or functionalities you think would enhance the platform for both parents and students? Students will be asked 'Do you think the interface of the online quiz competition platform is easy to use?' We will measure the number of times that the website developer or the students reported technical problems. We will also measure the participation rate of students during the online quiz competition period. |
During the post-questionnaire at 5th-6th weeks and during the phone interview at 10th-16th weeks.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effectiveness of intervention on tobacco-related knowledge (including ASPs)
Time Frame: During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
|
Students reported their opinions towards 5 statements in pre and post tests: [Pre-test] 1) Tar causes addiction; 2) Exposure to secondhand smoke increases the risk of cancer; 3) The harm from e-cigarettes is less than that of traditional cigarettes; 4) Tobacco companies use various flavours to attract children to use e-cigarettes; 5) The Hong Kong government has already banned the sale of heated tobacco products.
[Post-test] 1) Occasional smoking is harmless to health; 2) Exposure to secondhand smoke increases the risk of death; 3) E-cigarettes contain carcinogens; 4) Tobacco companies promote heated tobacco products through social media platforms; 5) The Hong Kong government has already banned the sale of e-cigarettes.
All the statements have 5 options from definitely no to definitely yes.
The options were recoded, as appropriate, with higher scores indicating knowing more about the harms and misleading marketing strategies of ASPs.
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During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Effectiveness of intervention on tobacco-related attitudes (including ASPs)
Time Frame: During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Students will report their opinions towards 5 statements: 1) Smokers are more stylish; 2) Adults should have the freedom to smoke in their homes; 3) Using e-cigarettes can bring a bit of enjoyment; 4) Tobacco companies have a contribution to society; 5) The government should implement a total ban on smoking.
All the statements have 5 options from definitely no to definitely yes.
The options will be recoded, as appropriate, with higher scores indicating knowing more about the harms and misleading marketing strategies of ASPs.
|
During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Effectiveness of intervention on tobacco-related intentions (including ASPs)
Time Frame: During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Students were asked: If one of your good friends offers you an 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?
There will be 5 options from definitely no to definitely yes.
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During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Effectiveness of intervention on SHS and THS exposure at home
Time Frame: During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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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?
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During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Effectiveness of intervention on tobacco use
Time Frame: During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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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?
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During the pre-questionnaire right before the intervention and post-questionnaire at 5th-6th weeks.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- coshdrama2324
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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