- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04259749
Testing Legally Feasible Options: Study 1
October 4, 2023 updated by: William Shadel, RAND
Experimentally Testing Legally Feasible Regulatory Options for Reducing the Impact of the Point-of-sale Retail Environment on Adolescent Tobacco Use
The overall aim of this research is to experimentally evaluate different, legally-viable approaches to reducing the impact of the point-of-sale (POS) retail environment on adolescent tobacco use risk.
This study will be investigating the regulations for four classes of tobacco products (cigarettes, e-cigarettes, smokeless tobacco, little cigars/cigarillos).
Study 1 (study 1 out of 3 proposed) will examine whether eliminating the sale of flavored tobacco products at POS reduced adolescents' tobacco use risk.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Tobacco advertising at retail point-of-sale (POS) includes promotional allowances that permit tobacco products to be advertised and sold at reduced cost to consumers (e.g., two-for-one specials); high visibility sale and therefore placement of hundreds of tobacco products on power walls; and the display of a large, diverse collection of poster advertisements on the exterior of the stores.
Adolescents are at significant risk for having repeated exposures to this tobacco rich POS environment and such exposures contribute to increases in adolescent tobacco use.
Although curbing the effect of the tobacco rich POS environment on adolescent tobacco use is a critical public health goal, some POS advertising regulations are unlikely to be viable in the United States because they impinge upon the tobacco industry's commercial free speech rights.
For example, eliminating the tobacco power wall is probably not a viable option in the US as it has been successfully challenged in court by the tobacco industry.
POS regulations that do not violate the industry's commercial free speech rights stand a better chance of being upheld by the courts.
For example, eliminating tobacco product price promotions, reducing the availability of tobacco products by restricting the sale of flavored products, and restricting how much door/window space tobacco product posters can occupy at POS, all have been implemented as feasible and legally defensible regulatory options at POS.
The evidence base supporting the efficacy of these initiatives is, however, almost non-existent - leaving them open to legal scrutiny.
The overall aim of this research is to experimentally evaluate different, legally-viable approaches to reducing the impact of the POS retail environment on adolescent tobacco use risk.
This research will be investigating the regulations for four classes of tobacco products (cigarettes, e-cigarettes, smokeless tobacco, little cigars/cigarillos): the extent to which eliminating tobacco product price promotions (Study 2), restricting how much door/window space tobacco posters can occupy at POS (Study 3), and eliminating the sale of flavored and/or mentholated tobacco products (Study 1) reduce adolescent tobacco-use risk.
Each study will evaluate for possible gender and race (African-American vs Caucasian) differences.
The studies will take place in the RAND StoreLab, a life-sized replica of a convenience store that was developed to experimentally evaluate how altering aspects of tobacco promotion at POS influences tobacco use.
The present record is for Study 1.
Study Type
Interventional
Enrollment (Actual)
267
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: William G Shadel, PhD
- Phone Number: 4489 412-683-2300
- Email: shadel@rand.org
Study Locations
-
-
Pennsylvania
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Pittsburgh, Pennsylvania, United States, 15213
- RAND
-
-
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
11 years to 17 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- ages 11-20, parental consent/adolescent assent for minors
Exclusion Criteria:
- any medical or psychiatric condition which would make compliance with the study protocol difficult (based on parent report).
- Previous participation (by either adolescent or parent) in a previous StoreLab study
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
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Status Quo
The StoreLab power wall will display all tobacco products.
|
No bans: All tobacco products are available
|
Experimental: Flavors Banned
The StoreLab will display tobacco products without characterizing flavors, but will allow mint and menthol products to be displayed.
|
Only flavored tobacco products are banned
|
Experimental: Flavors and Menthol Banned
The StoreLab will display only tobacco products without characterizing flavors; mint and menthol will not be displayed.
|
Only flavored tobacco products are banned
Mentholated products are banned
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of Participants Susceptible to Smoking Cigarettes After Shopping in the StoreLab (Non-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try an unflavored cigarette (unflavored = cigarettes without menthol or mint) anytime soon?", "Do you think you will smoke an unflavored cigarette (unflavored = cigarettes without menthol or mint) anytime in the next year?";
and "If one of your best friends offered you an unflavored cigarette (unflavored = cigarettes without menthol or mint), would you smoke it?".
Responses to each item are made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed for a total scale score.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Smoking Cigarettes After Shopping in the StoreLab (Menthol)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try a cigarette flavored with menthol or mint anytime soon?", "Do you think you will smoke a cigarette flavored with menthol or mint anytime in the next year?";
and "If one of your best friends offered you a cigarette flavored with menthol or mint, would you smoke it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of Participants Susceptible to Using Electronic Nicotine Delivery Device (ENDS) After Shopping in the StoreLab (Non-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try an unflavored vaping product soon?",
"Do you think you will use an unflavored vaping product anytime in the next year?";
and "If one of your best friends offered you an unflavored vaping product would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Outcome is number of participants susceptible to using ENDS after shopping in the StoreLab (non-flavored).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Electronic Nicotine Delivery Device (ENDS) After Shopping in the StoreLab (Sweet-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try a vaping product flavored with fruit, candy, alcohol or non-alcohol drink, or some other sweet flavor soon?", "Do you think you will use a vaping product flavored with fruit, candy, alcohol or non-alcohol drink, or some other sweet flavor anytime in the next year?";
and "If one of your best friends offered you a vaping product flavored with fruit, candy, alcohol or non-alcohol drink, or some other sweet flavor, would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scaled score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Electronic Nicotine Delivery Device (ENDS) After Shopping in the StoreLab (Menthol-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try a vaping product flavored with menthol or mint soon?", "Do you think you will use a vaping product flavored with menthol or mint anytime in the next year?";
and "If one of your best friends offered you a vaping product flavored with menthol or mint, would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Little Cigar/Cigarillos (LCC) After Shopping in the StoreLab (Non-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try an unflavored cigarillos/filtered cigar soon?", "Do you think you will use an unflavored cigarillos/filtered cigar anytime in the next year?";
and "If one of your best friends offered you an unflavored cigarillos/filtered cigar, would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Outcome is proportion of participants susceptible to using LCCs after shopping in the StoreLab (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Little Cigar/Cigarillos (LCC) After Shopping in the StoreLab (Sweet-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try a cigarillos/filtered cigar flavored with fruit, candy, alcohol or some other sweet flavor soon?", "Do you think you will use a cigarillos/filtered cigar flavored with fruit, candy, alcohol or some other sweet flavor anytime in the next year?";
and "If one of your best friends offered you a cigarillos/filtered cigar flavored with fruit, candy, alcohol or some other sweet flavor would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Little Cigar/Cigarillos (LCC) After Shopping in the StoreLab (Menthol-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try a cigarillos/filtered cigar flavored with menthol or mint soon?", "Do you think you will use a cigarillos/filtered cigar flavored with menthol or mint anytime in the next year?";
and "If one of your best friends offered you a cigarillos/filtered cigar flavored with menthol or mint would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Outcome is proportion of participants susceptible to using LCCs after shopping in the StoreLab (number of susceptible over number in condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Smokeless Tobacco After Shopping in the StoreLab (Non-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try unflavored smokeless tobacco soon?", "Do you think you will use unflavored smokeless tobacco anytime in the next year?";
and "If one of your best friends offered you unflavored smokeless tobacco, would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Smokeless Tobacco After Shopping in the StoreLab (Sweet-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try smokeless tobacco flavored with fruit soon?", "Do you think you will use smokeless tobacco flavored with fruit anytime in the next year?";
and "If one of your best friends offered you smokeless tobacco flavored with fruit, would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Proportion of Participants Susceptible to Using Smokeless Tobacco After Shopping in the StoreLab (Menthol-flavored)
Time Frame: There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Self-report items: "Do you think you will try smokeless tobacco flavored with menthol, mint, spearmint, or wintergreen soon?", "Do you think you will use smokeless tobacco flavored with menthol, mint, spearmint, or wintergreen anytime in the next year?";
and "If one of your best friends offered you smokeless tobacco flavored with menthol, mint, spearmint, or wintergreen, would you use it?".
Responses to each item were made on a 1 (Definitely Not) to 10 (Definitely Yes) scale and the three items were summed.
The total scale score was dichotomized: those who scored a '3' were recoded as '0' (not susceptible) and any scores greater than '3' were coded as '1' (susceptible).
Proportion of susceptible participants was the outcome (number susceptible over the total number of participants within condition).
|
There is one visit in this research: This variable is assessed at that visit, immediately after the experimental manipulation.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: William G Shadel, PhD, RAND
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)
January 16, 2020
Primary Completion (Actual)
May 31, 2022
Study Completion (Actual)
May 31, 2022
Study Registration Dates
First Submitted
February 2, 2020
First Submitted That Met QC Criteria
February 4, 2020
First Posted (Actual)
February 6, 2020
Study Record Updates
Last Update Posted (Actual)
October 30, 2023
Last Update Submitted That Met QC Criteria
October 4, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01CA236608 (U.S. NIH Grant/Contract)
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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