Address Tobacco Use Among Adolescents in Hong Kong

The University of Hong Kong (HKU)

Status: Unknown

Conditions: Tobacco Use

Treatments: Behavioral: Social norms campaign

Study type: Interventional

Funder types: Other

Identifiers

NCT03264144

17629016

Details and patient eligibility

About

This study will examine the effectiveness of a social norms campaign in correcting smoking misperceptions, reducing smoking susceptibility and changing smoking-related behaviours in Hong Kong adolescents.

Full description

The study involves a behavioural intervention with social norms approaches to correct smoking misperceptions, reduce smoking susceptibility and change smoking-related behaviours in Hong Kong adolescents. A 2-arm stratified clustered randomised controlled trial (RCT) will be conducted to evaluate the effectiveness of the intervention. A total of 18 secondary schools will be randomly selected from the 5 regions in Hong Kong and invited to the RCT. The schools will then be randomly allocated to intervention or control group in the ratio of 1:1. Secondary 1 to 5 (US Grade 7 to 11) students will be invited. Students in both intervention and control group will complete a baseline survey, and the intervention group will receive the intervention after the baseline. Intervention materials includes posters and table tents at school, flyers to students, and online banner on school website. The intervention adopts social norms approaches, and will highlight the prevalence of adolescents who do not smoke and have no intention to smoke. It will last for 2 months. Both intervention and control groups will complete follow-up surveys at 3 and 9 months. The control group will receive the intervention materials after the RCT.

Enrollment: 12,868 estimated patients

Sex: All

Ages: 11 to 20 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Local secondary schools that cover grades 1-6

Exclusion criteria

• International secondary schools
• Special schools for adolescents with visual, hearing or other physical impairments or disabilities

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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12,868 participants in 2 patient groups

Intervention

Experimental group

Description:

Students in the schools assigned to the intervention group will receive the intervention after the baseline survey. The intervention will be a social norms campaign involving posters, table tents, flyers and an online banner.

Treatment:

Behavioral: Social norms campaign

Control

No Intervention group

Description:

Students in the schools assigned to the control group will not receive anything during the randomised controlled trial. They will receive the intervention materials after the trial.