MedPath

Consumer Assessment of Tobacco Flavor and Odor

Active, not recruiting
Conditions
Current Vaper
Healthy Subject
Interventions
Behavioral: Behavioral Intervention
Other: Questionnaire Administration
Registration Number
NCT04358315
Lead Sponsor
Roswell Park Cancer Institute
Brief Summary

This trial studies consumer assessments of tobacco flavor and odor. This study will compare the ability of expert and consumer panels to identify and characterize flavors, determine threshold detection levels for individual and mixed flavors, and identify the dominant flavor of mixtures.

Detailed Description

PRIMARY OBJECTIVE:

I. Develop consumer (untrained) sensory panels to identify and assess characterizing flavors in electronic (e)-liquids.

OUTLINE:

Non-user panelists smell and user panelists puff flavored e-liquids and answer questions about the products.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
29
Inclusion Criteria
  • CONSUMER USER: Current daily vapers of products containing nicotine
  • CONSUMER USER: No concurrent use of other tobacco products
  • CONSUMER USER: General good health
  • CONSUMER USER: No allergies
  • CONSUMER USER: No self-reported taste or smell deficits
  • CONSUMER USER: Not pregnant or lactating
  • CONSUMER USER: No medications known to interfere with taste/smell
  • CONSUMER USER: Passing scores on the Brief Smell Identification Test (B-SIT), phenylthiocarbamine (PTC) and 6-n-propylthiouracil (PROP) smell and taste tests
  • CONSUMER USER: No positive diagnosis of COVID-19 within 30 days
  • CONSUMER NONUSER: No use of tobacco or nicotine products in the last year
  • CONSUMER NONUSER: General good health
  • CONSUMER NONUSER: No allergies
  • CONSUMER NONUSER: No self-reported taste or smell deficits
  • CONSUMER NONUSER: Not pregnant or lactating
  • CONSUMER NONUSER: No medications known to interfere with taste/smell
  • CONSUMER NONUSER: Passing scores on the Brief Smell Identification Test (B-SIT), phenylthiocarbamine (PTC) and 6-n-propylthiouracil (PROP) smell and taste tests
  • CONSUMER NONUSER: No positive diagnosis of COVID-19 within 30 days
Exclusion Criteria
  • CONSUMER USER: Outside age range
  • CONSUMER USER: Not current daily vapers
  • CONSUMER USER: Concurrent use of other tobacco products
  • CONSUMER USER: Fair or poor general health
  • CONSUMER USER: Allergies
  • CONSUMER USER: Self-reported taste or smell deficits
  • CONSUMER USER: Pregnant or lactating
  • CONSUMER USER: Medications known to interfere with taste/smell
  • CONSUMER USER: Failing scores on the Brief Smell Identification Test (B-SIT), phenylthiocarbamine (PTC) and 6-n-propylthiouracil (PROP) smell and taste tests
  • CONSUMER USER: Positive diagnosis of COVID-19 within 30 days
  • CONSUMER NONUSER: Outside age range
  • CONSUMER NONUSER: Use of tobacco or nicotine products in the last year
  • CONSUMER NONUSER: Fair or poor general health
  • CONSUMER NONUSER: Allergies
  • CONSUMER NONUSER: Self-reported taste or smell deficits
  • CONSUMER NONUSER: Pregnant or lactating
  • CONSUMER NONUSER: Medications known to interfere with taste/smell
  • CONSUMER NONUSER: Failing scores on the Brief Smell Identification Test (B-SIT), phenylthiocarbamine (PTC) and 6-n-propylthiouracil (PROP) smell and taste tests
  • CONSUMER NONUSER: Positive diagnosis of COVID-19 within 30 days

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Observational (smell or puff e-liquids)Behavioral InterventionAll panel participants smell and user panelists puff flavored e-liquids and answer questions about the products.
Observational (smell or puff e-liquids)Questionnaire AdministrationAll panel participants smell and user panelists puff flavored e-liquids and answer questions about the products.
Primary Outcome Measures
NameTimeMethod
Flavor combination thresholdsUp to 12 months

Subjects will rate a combination of two e-liquids combined

Flavor identification and evaluationUp to 12 months

Subjects will be asked to identify various concentrations of flavored e-liquids

Specific flavor detection thresholdsUp to 12 months

Subjects will rate intensity of odors of e liquids

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Roswell Park Cancer Institute

🇺🇸

Buffalo, New York, United States

© Copyright 2025. All Rights Reserved by MedPath