- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03380234
A Cluster-RCT of SHS Among Primary School Students (SHS-cRCT)
Reducing Exposure to Tobacco Smoke Among Primary School Students - a Cluster Randomised Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Around 12 primary schools in Hong Kong will be randomly selected and recruited and the 3 grades (P2-4) in each of the recruited schools will be randomly allocated to intervention or control arms. After the consenting process and baseline survey, we will conduct a 3-month intervention and then 2-month boosters which include 8 worksheets, around 15 online question quizzes and 30 WhatsApp messages. After 3-month and 6-month follow-up periods, we will assess the differences of children's exposure to environmental tobacco smoke (including SHS and THS at home, SHS at home from neighbours and SHS outside home), children's SHS-related knowledge and attitude, intention to smoke, respiratory symptoms, parents' smoking cessation, and family happiness. According to the results of baseline survey, we will also invite all the students exposed to SHS at home to provide their hair samples before intervention and at the 6th month in order to obtain objective results (hair nicotine measurements).
Aims of this study: (1) To reduce children's exposure to environmental tobacco smoke. (2) To reduce objectively measured exposure to tobacco smoke (hair nicotine) among children who are exposed to SHS at home at baseline. (6-month, laboratory test). (3) To promote SHS-related knowledge and attitudes, and avoidance of SHS among children. (4) To reduce children's intention to smoke. (5) To reduce children's respiratory symptoms. (6) To promote smoking cessation (past 7 days) of parents. (child report) (7) To promote children's perception of family happiness.
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
Genders Eligible for Study
Description
We will invite all P2-4 students from 12 schools randomly selected from the 100 schools (which watched the performance by Hong Kong Council on Smoking and Health) to participate in this cluster RCT, as they are able to understand simple questionnaires and other self-help intervention materials, yet remain very receptive to intervention activities from our experience.
Inclusion criteria for hair nicotine test:
1) exposed to secondhand smoke at home from smokers inside home in any of the past 7 days; 2) living with at least 1 smoker; 3) Never smoking or using e-cigarettes.
Study Plan
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
8 worksheets and around 15 online quizzes and 30 WhatsApp messages.
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Worksheets will be distributed to students for them and their parents to complete together.
During the first 3 months, the teachers will distribute 1 worksheet every two weeks to the intervention grades, and 1 worksheet in the 4th and 5th months as boosters.
The worksheets will deliver information about tobacco smoke, SHS and THS, inviting students and their family members to complete other interesting tasks together.
A mobile phone number of this study is also provided on the worksheets, through which participants can receive WhatsApp/WeChat/instant messages (1-2 times every week) designed to encourage behavioural change [15].
They can then forward selected messages to other members of their household, especially smokers.
At the end of each worksheet, a QR code is inserted.
By scanning this code, students or parents will be invited to answer 2-3 simple quizzes which allow us to assess students' knowledge obtained from the intervention materials and their avoidance of environmental tobacco smoke.
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Other: Control
Control students will receive the following minimal intervention to reduce their intention to smoke and SHS - a leaflet on smoking and SHS published by the Department of Health.
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A leaflet on smoking and SHS published by the Department of Health will be mailed to the control grades.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
To reduce children's exposure to environmental tobacco smoke.
Time Frame: 3 and 6-month
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In the 3th and 6th month, students will conduct a survey to assess their exposure to environmental tobacco smoke.
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3 and 6-month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
To reduce the hair nicotine levels of students who are exposed to SHS at home at baseline.
Time Frame: 6-month
|
At the 6th months, parents will be invited to post their children's hair for laboratory test and identify the change of the nicotine levels (objective measurement) before and after intervention.
|
6-month
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To promote SHS-related knowledge and attitudes, and avoidance of SHS among children.
Time Frame: 3 and 6-month
|
In the 3th and 6th month, students will conduct a survey to assess their SHS-related knowledge and attitudes, and avoidance of SHS.
|
3 and 6-month
|
To reduce children's intention to smoke.
Time Frame: 3 and 6-month
|
In the 3th and 6th month, students will conduct a survey to assess children's intention to smoke.
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3 and 6-month
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To reduce children's respiratory symptoms.
Time Frame: 3 and 6-month
|
In the 3th and 6th month, students will conduct a survey to assess children's respiratory symptoms.
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3 and 6-month
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To promote smoking cessation (past 7 days) of parents. (child report)
Time Frame: 6-month and 12-month3 and 6-month
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In the 3th and 6th month, students will conduct a survey to report their parents' smoking cessation.
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6-month and 12-month3 and 6-month
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To promote children's perception of family happiness.
Time Frame: 3 and 6-month
|
In the 3th and 6th month, students will conduct a survey to report their perception of family happiness.
|
3 and 6-month
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Sai Yin Ho, PhD, School of Public Health, The University of Hong Kong
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
- coshshs
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
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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