Trial on the Effect of E-cigarette Advertising on Cigarette Perceptions in Adolescents

Sponsor
Dartmouth-Hitchcock Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT03786042
Collaborator
National Cancer Institute (NCI) (NIH), Dartmouth College (Other)
132
1
2
34.1
3.9

Study Details

Study Description

Brief Summary

This research aims to investigate how exposure to advertising for Electronic Nicotine Delivery Systems (commonly called e-cigarettes) may lead to combustible smoking initiation in adolescents.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: E-cigarette ad exposure
  • Other: non e-cigarette TV commercials
N/A

Detailed Description

[3/14/2020]: Study recruitment temporarily halted due to the COVID-19 pandemic

Study Design

Study Type:
Interventional
Actual Enrollment :
132 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Does Exposure to Electronic Nicotine Delivery Systems Advertising Affect Positive Smoking Expectancies and Social Normative Beliefs About Smoking?
Actual Study Start Date :
Feb 4, 2019
Actual Primary Completion Date :
Dec 9, 2021
Actual Study Completion Date :
Dec 9, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: E-cigarette ad exposure

Participants in the e-cigarette ad exposure condition will view e-cigarette ads on the computer screen while having their eye movements tracked

Behavioral: E-cigarette ad exposure
Participants view a series of e-cigarette TV commercials

Sham Comparator: non e-cigarette ad exposure

Participants in the non e-cigarette ad exposure condition will view non e-cigarette ads on the computer screen while having their eye movements tracked

Other: non e-cigarette TV commercials
Participants view a series of non e-cigarette TV commercials

Outcome Measures

Primary Outcome Measures

  1. change in baseline in implicit positive smoking expectancies, measured by the implicit association test [baseline, within 5 minutes post intervention]

    Scores are measured by recording the amount of time (reaction time) it takes to categorize smoking-related words with positive (e.g., cool) and negative (e.g., cancer) words. Faster reaction times when categorizing smoking-related words with positive words is evidence of higher positive smoking expectancies.

  2. Amount of time spent looking at static smoking cues in e-cigarette advertisements [approximately 30 minutes post intervention]

    Eye-tracking will be used to measure the amount of time spent looking at static smoking cues in screen shots taken from e-cigarette advertisements. The amount time spent looking at a smoking cue is a measure how much attention was given to the smoking cue. The longer the looking time, the greater amount of attention.

  3. 7-item explicit positive smoking expectancies scale [approximately 30 minutes post intervention]

    Scores are measured on a 7-item scale. Positive smoking expectancies will be assessed using the following questions that follow the lead-in, "Please tell me how you feel about the following statements." "I think I would enjoy smoking"; "I think smoking would give me something to do when I'm bored"; "I think smoking would help me deal with problems or stress"; "I think smoking would help me stay thin"; "I think smoking would help me to feel more comfortable at parties"; "I think smoking would be relaxing"; and "I think smoking would make me look older." Responses are yes/no. Responses are coded as "1" for yes and "0" for no. Responses are then summed for a maximum positive smoking expectancy score out of 7. Higher scores mean higher positive smoking expectancies.

  4. 11-item scale that measures social normative beliefs about smoking [approximately 30 minutes post intervention]

    This 11-item scale assess social normative beliefs about smoking related to 1) perceived disapproval from family/friends, 2) perceived popularity among successful/elite, and 3) perceived prevalence. Disapproval scale questions are answered using a 4-point Likert scale (1 = Strongly disagree; 4 = Strongly agree). A total disapproval score (ranging from 1 to 4) is calculated by averaging responses to each question. Higher values indicate a higher disapproval score. Popularity scale questions are answered using a 4-point Likert scale (1 = Strongly disagree; 4 = Strongly agree). A total popularity score (ranging from 1 to 4) is calculated by averaging responses to each question. Higher values indicate a higher popularity score. Prevalence scale questions are answered using a percent scale from 0 - 100% in 10% increments. A total prevalence scale (from 0 to 100) is calculated by averaging the responses to each question. Higher values indicate a higher prevalence score.

  5. A 3-item scale that measures adolescent smoking susceptibility [approximately 30 minutes post intervention]

    This 3-item instrument is used to predict which never smokers are likely to start smoking by measuring their curiosity to use tobacco products. Item responses are on a 4-point Likert scale (definitely yes, probably yes, probably not, definitely not). To classify a respondent as not susceptible to smoking, the respondent must indicate "definitely not" to all four items. Any other response to any item classifies a respondent as "susceptible."

Secondary Outcome Measures

  1. Amount of time looking at dynamic smoking cues in e-cigarette advertisements [During the intervention, approximately 15 minutes post baseline]

    Eye-tracking will be used to measure the total amount of time spent looking in realtime at smoking cues in TV commercials for e-cigarettes. The amount of time looking at smoking cues will be a measure of the amount of attention given to smoking cues. The longer the amount of time spent looking at smoking cues indicates that a greater amount of attention was given to the smoking cues.

  2. 18-item scale that measures character attributes of actors that appeared in the commercials [approximately 30 minutes post intervention]

    Character Attributes will be collected using a scale that measures participants beliefs about character attributes using the lead in: "I think [Character Name] is: " using a 5-point Likert (1 = strongly disagree; 5 = strongly agree). There is a total of 6 attributes assessed: 1) smart (smart, intelligent, stupid), 2) successful (successful, achieves goals, gets what he/she wants), 3) attractive (physically attractive, ugly, good-looking), 4) funny (funny, humorous, makes me laugh), 5) respected (respected by others, receives approval, criticized by others), and 6) popular (has lots of friends, well liked, gets support from others). A total score (form 1 to 5) for each scale is calculated by averaging responses for each question within that scale. For each scale, a higher total score indicates higher beliefs about that attribute.

  3. 5-item scale that measure how much participants wish to be like the actors appearing in the commercials. [approximately 30 minutes post intervention]

    This 5-item is scale is used to quantify how much a participant would like to be like an actor appearing in a commercial. Questions are rated on a 5-point Likert scale (1 = Strongly Disagree; 5 = Strongly agree). A total identification score (from 1 to 25) is calculated by summing the responses to each question. A higher total score indicates a higher level of wishful identification.

  4. 13-item scale to measure risk perception about cigarette use [approximately 30 minutes post intervention]

    This 13-item scale measures risk perceptions associated with cigarette use. Questions are answered using a sliding percent scale from 0 - 100% in 10% increments. A risk perception scale is calculated (from 0 to 100) by averaging the responses to each question. Higher values indicate a higher risk perception.

  5. 13-item scale to Measure risk perception about e-cigarette use [approximately 30 minutes post intervention]

    This 13-item scale measures risk perceptions associated with e-cigarette use. Questions are answered using a sliding percent scale from 0 - 100% in 10% increments. A risk perception scale is calculated (from 0 to 100) by averaging the responses to each question. Higher values indicate a higher risk perception.

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Exclusion Criteria:
  • Exclusion criteria will include inadequate English proficiency, and diagnosis of a learning or vision disorder.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dartmouth-Hithchock Medical Center Lebanon New Hampshire United States 03756

Sponsors and Collaborators

  • Dartmouth-Hitchcock Medical Center
  • National Cancer Institute (NCI)
  • Dartmouth College

Investigators

  • Principal Investigator: James Sargent, MD, Geisel School of Medicine at Dartmouth College
  • Principal Investigator: Diane Gilbert-Diamond, ScD, Geisel School of Medicine at Dartmouth College

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Diane Gilbert-Diamond, Associate Professor, Dartmouth-Hitchcock Medical Center
ClinicalTrials.gov Identifier:
NCT03786042
Other Study ID Numbers:
  • D19034
  • 1R21CA232054-01
First Posted:
Dec 24, 2018
Last Update Posted:
May 27, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Diane Gilbert-Diamond, Associate Professor, Dartmouth-Hitchcock Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 27, 2022