- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05482581
The Impact of Policies Regarding E-cigarette on Adolescents and Young Adults' Cognition and Behavior for E-cigarette
The Impact of Policies Regarding E-cigarette(Trial) on Adolescents and Young Adults' Cognition and Behavior for E-cigarette: A Convergent Parallel Mixed-method Study Based on KABP Model.
Study Overview
Detailed Description
Mixed method will be used: the cross-sectional surveys will be conducted on the demographic characteristics, e-cigarette use intentions, e-cigarette use behaviors, attitudes towards e-cigarette , knowledge of e-cigarette harm, reasons for using e-cigarette and the degree of understanding of the new regulations on e-cigarette control ; semi-structured interviews will be conducted with some young people and adolescents interviewed by using phenomenology and qualitative research methods, and the content of the interview will be summarized and analyzed. The primary and secondary categories and dimensions are coded; the analysis results of quantitative data and qualitative data are combined to explain the influencing mechanism of the trial implementation of e-cigarette regulatory regulations on youth and adolescents' cognition of electronic cigarettes and changes in their use behaviors.
Using the network epidemiological method, use the "drop-down word deep mining function" of the 5188 marketing big data website to obtain the relevant keywords of "electronic cigarette", and use the Baidu index and 360 index tools to explore the retrieval behavior of electronic cigarettes and related electronic cigarettes Event trace changes.
Combined with online epidemiological data and mixed method study results, summarize the changes in youth and adolescents' cognition and use of e-cigarettes before and after the promulgation of the new regulations, and provide a theoretical basis for formulating e-cigarette control policies in the future.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Guangdong
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Guangzhou, Guangdong, China, 510080
- Recruiting
- XIAW
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 14-35 years old;
- Being able to read and write in Chinese.
Exclusion Criteria:
- Those who are unable to communicate due to serious mental or physical illnesses such as deafness, unclear consciousness due to mental illness, etc.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Questionnaires assessed adolescents and young adults
①14-35 years old; ②Being able to read and communicate in Chinese.
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Participants will be asked to respond to the demographic information sheet,e-cigarette using characteristics sheet,awareness of e-cigarettes sheet;,willingness to use e-cigarettes sheet, knowledge, attitudes and cognitions related to e-cigarettes sheet, awareness of new regulations on e-cigarette control sheet.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of e-cigarette use
Time Frame: Baseline
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Measured by the questionnaire including the following items:e-cigarette use, the daily amount of e-cigarette, the age of first e-cigarette use, the reasons for first e-cigarette use, the place where participant first smoked e-cigarette, e-cigarette dependence , the type and amount of other tobacco products used and the daily smoking place.
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Baseline
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Change of e-cigarette use
Time Frame: 6 month follow up
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Measured by the questionnaire including the following items:e-cigarette use, the daily amount of e-cigarette, the age of first e-cigarette use, the reasons for first e-cigarette use, the place where participant first smoked e-cigarette, e-cigarette dependence , the type and amount of other tobacco products used and the daily smoking place.
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6 month follow up
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Change of knowledge,attitudes and cognitions related to e-cigarette
Time Frame: Baseline
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The questionnaire items were compiled according to the literature review content, and the questionnaire contained 20 items in total.
Six items were related to e-cigarette knowledge, five items are related to the susceptibility of e-cigarettes,eight items are related to the perceived harmfulness of e-cigarettes, one item is related to the perceived relative risk.
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Baseline
|
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Change of knowledge,attitudes and cognitions related to e-cigarette
Time Frame: 6 month follow up
|
The questionnaire items were compiled according to the literature review content, and the questionnaire contained 20 items in total.
Six items were related to e-cigarette knowledge, five items are related to the susceptibility of e-cigarettes,eight items are related to the perceived harmfulness of e-cigarettes, one item is related to the perceived relative risk.
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6 month follow up
|
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Change of awareness of new regulations on e-cigarette control
Time Frame: Baseline
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Measured by a yes-or-no question in the questionnaire,and those who answered yes can be considered to be aware of e-cigarette regulations.
|
Baseline
|
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Change of awareness of new regulations on e-cigarette control
Time Frame: 6 month follow up
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Measured by a yes-or-no question in the questionnaire,and those who answered yes can be considered to be aware of e-cigarette regulations.
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6 month follow up
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
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
Keywords
Other Study ID Numbers
- wjn-ChiCTR2200060895
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- SAP
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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