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Enrolling by invitation NCT07129265

Understanding Vape Marketing Study

Observational E-cigarette Vaping Tobacco Nicotine

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Working group, Focus group.
Who it may be relevant to
Registry conditions: E-cigarette, Vaping, Tobacco, Nicotine. Basic parameters: from 13 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Countering E-cigarette Marketing in the Retail Environment Among Adolescents and Young Adults

Overview

The purpose of this study is to develop an electronic cigarette (e-cigarette) counter-marketing lesson for adolescents. The lesson will involve short videos designed to improve adolescents' cognition of e-cigarette marketing in the retail environment with the overall goal of reducing their susceptibility to use, intent to use, and actual use of e-cigarettes. Through this study, the study team will identify and refine the key messages that would make this lesson acceptable, feasible to implement, and effective in altering e-cigarette-related perceptions and potentially behaviors.

Detailed description

This research comprises of 2 qualitative activities:

1. Working group: The study team will purposively invite a convenience sample of expert members (including middle/high school students, young adults, an educator, a parent, and curriculum design experts) to convene multiple times over several weeks (3 meetings via videoconference). The working group will convene to view preliminary results from formative research, collaborate on the development of this lesson curriculum, and otherwise offer meaningful input on study materials. 2. Focus groups: A convenience sample of adolescents/young adults will be enrolled to participate in a focus group via videoconferenc . Each participant will only participate in a single focus group. There will be \~4 participants in each focus group, and 9 focus groups overall. Before their focus group, each participant will complete a brief online survey that collects sociodemographics and outcome measures data. During their focus group, each participant will be asked to view and describe their opinion about broad counter-marketing strategies, messages, and participate in viewing mood-boards and video-storyboards using these messages. A trained facilitator will follow a standardized discussion guide to lead the focus groups.

These activities will occur sequentially over about 6 months. At the 6-month time point, the study team will have met the study's primary aim of having developed the e-cigarette counter-marketing lesson.

Interventions

  • Other Working group
    Participants will: 1) take a 10-min demographic survey; 2) join 3 x 60-min working group meetings in which they will review preliminary results, collaborate on curriculum design, and provide feedback; and 3) respond to prompts in 3 emails (approx 5-10 mins each).
  • Other Focus group
    Participants will take a 10-min demographic survey and join 1 x 30-min focus group meeting in which they will provide feedback on the curriculum in development.

Primary outcome measures

  • Development of an e-cigarette counter-marketing lesson focused on the retail environment [Time frame: At 6 months]

Eligibility criteria

WORKING GROUP MEMBERS

\*Inclusion criteria

Youth participants:

  • Middle school students may be 13-15 years
  • High schoolers may be 16-18 years
  • Young adults may be 19-29 years
  • Provide a phone number for at least one backup contact (e.g, parent/guardian)

Curriculum design experts:

  • Experience of at least 1 year in tobacco prevention or relevant public health field

Parent:

  • Parent of a child who has e-cigarette use history or is currently using (preferred, but not essential)

Educator:

  • Currently employed as teacher at a middle/high school All participants
  • Provide their cell phone number and email address
  • Fluent in English

\*Exclusion criteria

  • Express inability to participate consistently across study working group meetings.

FOCUS GROUP PARTICIPANTS

\*Inclusion criteria

  • Adolescents and young adults ages 13-21 years
  • Fluent in English
  • Provide their cell phone number and email address
  • Provide a phone number for at least one backup contact

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Boston Children's Hospital — Boston

Identifiers

NCT: NCT07129265 · 25-232 · 5R00CA267477

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗