The Impact of Policies Regarding E-cigarette on Adolescents and Young Adults' Cognition and Behavior for E-cigarette

February 8, 2023 updated by: Wei XIA, PhD, Sun Yat-sen University

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.

Based on the Knowledge,Attitude,Belief and Practice model(KABP model), this study intends to use a mixed method to explore the influencing mechanism of youth and adolescents' cognition and behavior for e-cigarette before and after the promulgation of the new regulations on e-cigarette . Information from network epidemiology (including network links, text, images, audio, video, etc.) was captured to expand the data abundance, and the retrieval behavior of e-cigarettes and the trajectory changes of e-cigarette-related events were explored. Finally, summarize the data, integrate and explain the influencing mechanism of youth and adolescents' attention and cognition on e-cigarette, and provide ideas for subsequent e-cigarette control, as well as theoretical and practical basis for relevant departments to formulate corresponding policies.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

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

Observational

Enrollment (Anticipated)

453

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China, 510080
        • Recruiting
        • XIAW

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 35 years (ADULT, CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Using an online and offline multi-channel model, participants who meet the eligibility criteria are invited to join the study.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Questionnaires assessed adolescents and young adults
①14-35 years old; ②Being able to read and communicate in Chinese.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of e-cigarette use
Time Frame: Baseline
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.
Baseline
Change of e-cigarette use
Time Frame: 6 month follow up
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.
6 month follow up
Change of knowledge,attitudes and cognitions related to e-cigarette
Time Frame: Baseline
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.
Baseline
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.
6 month follow up
Change of awareness of new regulations on e-cigarette control
Time Frame: Baseline
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
Change of awareness of new regulations on e-cigarette control
Time Frame: 6 month follow up
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.
6 month follow up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 27, 2022

Primary Completion (ANTICIPATED)

January 1, 2024

Study Completion (ANTICIPATED)

February 1, 2024

Study Registration Dates

First Submitted

July 24, 2022

First Submitted That Met QC Criteria

July 29, 2022

First Posted (ACTUAL)

August 1, 2022

Study Record Updates

Last Update Posted (ACTUAL)

February 10, 2023

Last Update Submitted That Met QC Criteria

February 8, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The non-identified individual participant data will be shared after the outcomes have been published.

IPD Sharing Time Frame

After the publication of the study

IPD Sharing Access Criteria

Researchers should contact the PI for approval of the study protocol.

IPD Sharing Supporting Information Type

  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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