Attitudes and Smoking Perceptions in the Real Environment

NCT ID: NCT06617520

Last Updated: 2025-08-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

29 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-15

Study Completion Date

2025-05-30

Brief Summary

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This study will measure appeal and reinforcement for different flavored little cigars/cigarillos (LCCs) in young adults in the laboratory and at-home, via ecological momentary assessment (daily smart-phone surveys)

Detailed Description

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Participants will attend 4 laboratory sessions that differ by cigarillo smoked: own brand and a then commercially available study cigarillo (Garcia y Vega game cigarillo) in tobacco flavor, concept flavor, and characterizing flavor. Consistent with our work and other's published work8-10, a baseline (BL) period will measure appeal to smoking one's usual brand cigarillo in their home environment for 7 days and then once in the laboratory (\>12-hour abstinence), at the end of the 7 days. Participants will then undergo 3 experimental conditions (counterbalanced, within-subjects): (1) 7 days smoking a concept flavored study cigarillo; (2) 7 days smoking a characterizing flavored study cigarillo; and (3) 7 days smoking a tobacco flavored study cigarillo. Participants will be instructed to switch their usual brand cigarillo for the assigned study cigarillo for each 7-day period. Other tobacco use will be allowed during that time without specific instruction to model real-world behavior. On the last day of each 7-day period of "take home" use, abstinent participants (\>12 hours) will smoke the assigned study cigarillo in the lab ad libitum, where subjective effects (e.g., satisfaction, craving reduction, psychological reward, throat hit), smoke exposure (CO boost), and behavior (e.g., number of puffs) will be assessed During each 7-day period of exposure, participants will complete assessments of cigarillo and other tobacco use and subjective effects to cigarillo use via once daily EMA.

Conditions

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Tobacco Use

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Tobacco flavor cigarillo

A participant will use a tobacco flavored cigarillo at home for 7-days, as they wish, and then smoke it once in the laboratory

Group Type EXPERIMENTAL

Cigarillo flavor type

Intervention Type OTHER

Participants will complete a within-subjects design that varies by cigarillo smoked: tobacco flavor, concept flavor, and characterizing flavor

Concept flavor cigarillo

A participant will use a concept flavored cigarillo at home for 7-days, as they wish, and then smoke it once in the laboratory

Group Type EXPERIMENTAL

Cigarillo flavor type

Intervention Type OTHER

Participants will complete a within-subjects design that varies by cigarillo smoked: tobacco flavor, concept flavor, and characterizing flavor

Characterizing flavor

A participant will use a characterizing flavored cigarillo at home for 7-days, as they wish, and then smoke it once in the laboratory

Group Type EXPERIMENTAL

Cigarillo flavor type

Intervention Type OTHER

Participants will complete a within-subjects design that varies by cigarillo smoked: tobacco flavor, concept flavor, and characterizing flavor

Interventions

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Cigarillo flavor type

Participants will complete a within-subjects design that varies by cigarillo smoked: tobacco flavor, concept flavor, and characterizing flavor

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Ages18 to 34
* Smoke little cigars/cigarillos (LCCs) "some days" or "everyday"
* Ability to read English at an 8th grade level or higher
* No immediate plans to quit using tobacco

Exclusion Criteria

* Current use of nicotine replacement therapy (NRT)
* Pregnant, planning to become pregnant, or currently breastfeeding
* Past or current self-reported clinically significant heart disease or hypertension, or other smoking-related disease (by history) that preclude successful study completion Inability to abstain from nicotine/tobacco products for at least 12 hours prior to each of two study sessions
* Report using the study cigarillo brand as their preferred brand (as this will likely unduly influence their perceptions)
* Unwillingness to use "untipped" (e.g., plastic or wood tip) little cigars/cigarillos.
Minimum Eligible Age

18 Years

Maximum Eligible Age

34 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Presbyterian Health Foundation

UNKNOWN

Sponsor Role collaborator

University of Oklahoma

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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TSET Health Promotion Research Center

Oklahoma City, Oklahoma, United States

Site Status

Countries

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United States

Other Identifiers

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ST116745

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

ASPIRE

Identifier Type: -

Identifier Source: org_study_id

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