Understanding Risk Perception Behaviour and Attitudes Related to Other New Tobacco Products Among Youth

  • STATUS
    Recruiting
  • participants needed
    390
  • sponsor
    The University of Hong Kong
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Updated on 5 August 2020
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tobacco product

Summary

To understand the risk perception, behaviour, and attitudes related to electronic cigarettes and other tobacco products among youth.

Description

Phase I Individual qualitative interviews will be conducted to understanding the needs and concerns of youth smokers of e-cigarette or other new tobacco products, including their risk perceptions, and the behaviour, attitudes, and experiences related to these products.

Phase II The findings from the interview in phase I will guide the development of a structure questionnaire for a cross-sectional survey to further explore the behaviour, attitudes, and experiences related to e-cigarette or other new tobacco products among youth.

The findings of this study have important implications for research and clinical practice. Understanding how youth smokers perceive the risks of using e-cigarette and other new tobacco products, and their behaviour, attitudes, experiences related to smoking to help them achieve smoking abstinence. Moreover, the results of this study can understand the misconceptions about e-cigarette and other new tobacco product among youth, increase their perception of the risks of continued smoking and benefits of quitting.

Details
Condition Smoking Cessation, Smoking Cessation
Age 12years - 25years
Treatment Individual qualitative interview, cross-sectional survey study
Clinical Study IdentifierNCT04416698
SponsorThe University of Hong Kong
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Youth smokers who contacted the Youth Quitline will be eligible to be included in this study if they (1) are ethnic Chinese; (2) are aged 25 years; (3) are ever user of e-cigarette or any new tobacco products; and (4) spoke Cantonese

Exclusion Criteria

psychologically or physically unable to communicate
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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