Shrinking the Size of the Tobacco Power Wall and Restricting the Number of Tobacco Products Displayed to Reduce Adolescent Tobacco Use

Sponsor
RAND (Other)
Overall Status
Recruiting
CT.gov ID
NCT04632030
Collaborator
(none)
900
1
3
31
29

Study Details

Study Description

Brief Summary

The overall aim of this research is to experimentally evaluate the extent to which reducing the size of the tobacco power wall and the number of tobacco product units displayed influences tobacco use risk in adolescents.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Tobacco power wall size and tobacco products displayed
N/A

Detailed Description

This experiment will take place in the RAND StoreLab (RSL), a life-sized replica of a convenience store that we developed to evaluate how altering aspects of tobacco promotion at POS influences tobacco use risk during simulated shopping experiences. The study will use a between-subjects design, in which adolescents are randomly assigned to shop in the RSL under one of three conditions: (1) Large power wall/ multiple product units displayed; (2) Small power wall/multiple product units displayed; and (3) Small power wall/single product units displayed. We will consider the effect of these power wall alterations on risk of use of four classes of tobacco products: cigarettes, electronic nicotine delivery devices, cigarillos, and smokeless tobacco. Tobacco use risk will be indexed by: attention to the tobacco power wall, perceived tobacco use norms, perceived availability of tobacco, and tobacco use intentions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
900 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Shrinking the Size of the Tobacco Power Wall and Restricting the Number of Tobacco Products Displayed to Reduce Adolescent Tobacco Use
Actual Study Start Date :
Oct 30, 2020
Anticipated Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Control

The tobacco power wall and number of products appears in a typical format: large power wall with a large number of products (defined here as three large cabinets)

Behavioral: Tobacco power wall size and tobacco products displayed
The intervention varies the size of the tobacco power wall and number of tobacco products displayed on it.

Experimental: Small

The tobacco power wall and number of tobacco products appear in their smallest format: small power wall with a small number of products displayed (defined here as one large cabinet)

Behavioral: Tobacco power wall size and tobacco products displayed
The intervention varies the size of the tobacco power wall and number of tobacco products displayed on it.

Experimental: Medium

The tobacco power wall and number of tobacco products appear in a format sized between the control and small conditions: a medium sized power wall with a medium number of products displayed (defined here as two large cabinets).

Behavioral: Tobacco power wall size and tobacco products displayed
The intervention varies the size of the tobacco power wall and number of tobacco products displayed on it.

Outcome Measures

Primary Outcome Measures

  1. Tobacco use intentions [within 5 minutes of the intervention]

    intentions to use tobacco, as assessed by a three item scales with type of tobacco product inserted in brackets: 1) Do you think you will try [tobacco product] soon?; 2) Do you think you will try [tobacco product] in the next year; & 3) If one of your best friends offered you [tobacco product] would you use it? Responses to each item are made on a 10-point scale where 1 = definitely not; and 10 = definitely yes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
11 Years to 20 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • between the ages of 11 and 20
Exclusion Criteria:
  • any medical or psychological condition that would make participation in the procedures of the study difficult (based on self-report).

Contacts and Locations

Locations

Site City State Country Postal Code
1 RAND Pittsburgh Pennsylvania United States 15213

Sponsors and Collaborators

  • RAND

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
William Shadel, Senior Behavioral Scientist, RAND
ClinicalTrials.gov Identifier:
NCT04632030
Other Study ID Numbers:
  • R01DA050972
First Posted:
Nov 17, 2020
Last Update Posted:
May 2, 2022
Last Verified:
Apr 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

Study Results

No Results Posted as of May 2, 2022