UNC Tobacco Convenience Store

UNC Tobacco Convenience Store Study

The main purpose of this trial is to evaluate the impact of a menthol cigarette ban accompanied by a quit smoking campaign on tobacco purchasing behavior. Investigators will conduct a randomized clinical trial with ~1,185 US adults (ages 21+ years) who currently smoke menthol cigarettes.

Study Overview

Detailed Description

This trial aims to determine whether a quit smoking campaign amplifies the impact of a simulated menthol cigarette ban. The trial will enroll ~1,185 adults ages 21 years and older who currently smoke menthol cigarettes. Participants will attend 2 in-person study visits at our experimental store, spaced approximately 1 week apart. The store will be stocked with a variety of tobacco products, food, non-alcoholic beverages, and household goods. At the first visit, participants will provide written informed consent and will be randomized to 1 of 3 trial arms, described further below. At both study visits, participants will shop for items in the store and complete computer surveys. Researchers will record in-store purchases and other self-reported measures will be assessed via the computer surveys. In between the in-person study visits, participants will receive ads via text message based on their trial arm.

Study Type

Interventional

Enrollment (Estimated)

1185

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 Locations

    • North Carolina
      • Raleigh, North Carolina, United States, 27609
        • Recruiting
        • UNC Mini Mart
        • Principal Investigator:
          • Marissa Hall, PhD
        • Contact:

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Are ages 21 years and older
  • Smoke cigarettes currently (i.e. currently smoke some days or every day and have smoked at least 100 cigarettes in their lifetime)
  • Smoke menthol cigarettes
  • Purchased menthol cigarettes in a store in the past month
  • Read and speak English
  • Can complete a survey on a computer without help
  • Can receive images by text message
  • Can attend 2 in-person appointments involving shopping tasks and computer surveys

Exclusion Criteria:

  • Are pregnant
  • Are breastfeeding
  • Enrolled currently in another research study about quitting smoking

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control
Menthol cigarettes and flavored little cigars and cigarillos will be available for purchase in the store. Participants will receive control ads about a neutral topic (i.e., password security) via text message. These ads will also be displayed inside the store during the shopping tasks.
Experimental: Menthol ban + campaign
Menthol cigarettes and flavored little cigars and cigarillos will not be available for purchase in the store. Participants will receive quit smoking campaign ads via text message. These ads will also be displayed inside the store during the shopping tasks.
Experimental: Menthol ban
Menthol cigarettes and flavored little cigars and cigarillos will not be available for purchase in the store. Participants will receive control ads about a neutral topic (i.e., password security) via text message. These ads will also be displayed inside the store during the shopping tasks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Purchasing any combustible tobacco products
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using purchase data for combustible tobacco products, defined as any cigarettes or little cigars and cigarillos. Response options are "No" (coded as 0) and "Yes" (coded as 1).
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Expenditures on combustible tobacco products
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using purchase data for combustible tobacco products, defined as any cigarettes or little cigars and cigarillos. This measure is in US dollars, ranging from $0 to $70.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Purchasing any non-combustible tobacco products (substitution effects)
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using purchase data on whether participants bought any non-combustible tobacco products, defined as any e-cigarettes, smokeless tobacco, or nicotine pouches. Response options are "No" (coded as 0) and "Yes" (coded as 1).
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Attempted to quit smoking
Time Frame: Assessed 1 time, approximately 1 week after enrollment.
Measured using 1 survey item: "In the last week, did you stop smoking cigarettes for 1 day or longer because you were trying to quit smoking?" Response options are "No" coded as 0) and "Yes" (coded as 1).
Assessed 1 time, approximately 1 week after enrollment.
Forgoing cigarette use
Time Frame: Assessed 1 time, approximately 1 week after enrollment.
Measured using 2 survey items (e.g., " In the last week, how often have you stopped yourself from having a cigarette because you wanted to smoke less?"). The 5-point response scale ranges from "Never" coded as 0, to "10 or more times", coded as 10. Researchers will average responses to the 2 survey items to create a scale score. Higher scores indicate greater frequency of forgoing cigarettes.
Assessed 1 time, approximately 1 week after enrollment.
Intentions to quit smoking
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 3 survey items (e.g., "How interested are you in quitting smoking cigarettes in the next 4 weeks?"). The 4-point response scale ranges from low intentions (coded as 1) to high intentions (coded as 4). Researchers will average responses to the 3 survey items to create a scale score. Higher scores indicate greater intentions to quit smoking.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Injunctive norms for quitting smoking
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 3 survey items (e.g., "People who are important to me think I should quit smoking."). The 5-point response scale ranges from "Strongly disagree" (coded as 1) to "Strongly agree" (coded as 5). Researchers will average responses to the 3 survey items to create a scale score. Higher scores indicate greater injunctive norms for quitting smoking.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Reactance towards cigarette options
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 3 survey items (e.g., "I was annoyed by the cigarette options in the Mini Mart."). The 5-point response scale ranges from "Strongly disagree" (coded as 1) to "Strongly agree" (coded as 5). Researchers will average responses to the 3 survey items to create a scale score. Higher scores indicate greater reactance toward cigarette options.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Reactance towards ads
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 3 survey items (e.g., "The ads annoyed me."). The 5-point response scale ranging from "Strongly disagree" (coded as 1) to "Strongly agree" (coded as 5). Researchers will average responses to the 3 survey items to create a scale score. Higher scores indicate greater reactance toward ads.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Stigma from cigarette options
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 1 survey item (i.e., "How much did the cigarette options in the Mini Mart make you feel judged by other people for smoking?"). The 5-point response scale ranges from "Not at all" (coded as 1) to "A great deal" (coded as 5) to create a scale score. Higher scores indicate greater stigma from cigarette options.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Stigma from ads
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 1 survey item (i.e., "How much did the ads make you feel judged by other people for smoking?"). The 5-point response scale ranges from "Not at all" (coded as 1) to "A great deal" (coded as 5). Higher scores indicate greater stigma from ads.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Targeted benefits of quitting smoking
Time Frame: Assessed 2 times approximately 1-week apart, starting on the day of enrollment.
Measured using 6 survey items (e.g., "If you were to stop smoking, how likely would you be to get more quality time with loved ones?"). The 5-point response scale ranges from "Not at all likely" (coded as 1) to "Extremely likely" (coded as 5). Researchers will average responses to the 7 survey items to create a scale score. Higher scores indicate greater targeted benefits of quitting smoking.
Assessed 2 times approximately 1-week apart, starting on the day of enrollment.

Collaborators and Investigators

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

Investigators

  • Study Director: Marissa G. Hall, PhD, University of North Carolina, Chapel Hill

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)

April 20, 2026

Primary Completion (Estimated)

April 1, 2028

Study Completion (Estimated)

April 1, 2028

Study Registration Dates

First Submitted

March 4, 2026

First Submitted That Met QC Criteria

March 4, 2026

First Posted (Actual)

March 9, 2026

Study Record Updates

Last Update Posted (Actual)

April 27, 2026

Last Update Submitted That Met QC Criteria

April 23, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 24-0398
  • U54DA060049 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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