MedTrace Logo

Responses of Adults Smoking Nondaily and Daily in the Experimental Tobacco Marketplace

NCT06988371 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 695

Last updated 2025-10-14

No results posted yet for this study

Summary

The goal of this project is to learn about the potential impact of tobacco regulations that could affect the availability of tobacco products among adults who smoke nondaily and daily. Nondaily smoking is increasingly common and tobacco regulation research should consider how FDA actions may impact this group. Participants will be asked to complete online surveys and tests, online shopping sessions in a simulated Experimental Tobacco Marketplace. Reactions and decisions of adults who smoke nondaily and daily will be compared.

Conditions

  • Tobacco Use
  • Cigarette Use

Interventions

BEHAVIORAL

Reduced nicotine regulatory environment

In this regulatory environment, participants' usual combustible cigarette will not be available in the Experimental Tobacco Marketplace and reduced nicotine content cigarettes will be the only available combustible cigarette.

BEHAVIORAL

Restriction on characterizing flavors in combustible nicotine products

In this regulatory environment, menthol and other characterizing flavors in combustible nicotine products will not be available in the Experimental Tobacco Marketplace. Tobacco- or no-flavored combustible nicotine products will be the only combustible nicotine products available.

BEHAVIORAL

Restriction on characterizing flavors in noncombustible nicotine products

In this regulatory environment, menthol and other characterizing flavors in noncombustible nicotine products will not be available in the Experimental Tobacco Marketplace. Tobacco- or no-flavored noncombustible nicotine products will be the only noncombustible nicotine products available.

Sponsors & Collaborators

  • National Institute on Drug Abuse (NIDA)

    collaborator NIH

  • Bethany Shorey Fennell

    lead OTHER

Principal Investigators

  • Bethany Shorey Fennell, PhD · University of Kentucky

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-08-18
Primary Completion
2025-08-29
Completion
2025-08-29

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06988371 on ClinicalTrials.gov