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Impact of Cigar Flavor in Dual Users

Primary Purpose

Tobacco Use Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Flavored filtered cigars
Unflavored filtered cigars
Sponsored by
UConn Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Tobacco Use Disorder focused on measuring Dual Tobacco Use, Smoking, Cigar Smoking, Cigarette Smoking

Eligibility Criteria

21 Years - 34 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Current regular dual uses of filtered cigars and cigarillos (FCs) and cigarettes defined as; (a) report smoking cigarettes at least weekly in the past 30 days, (b) report smoking unaltered FC (without marijuana) at least weekly in the past 30 days; and (c)report cigarette and cigar use at their current rate (or more frequently) for ≥ 3 months.
  • Able to read, speak, and understand English
  • Age 18-34 years
  • Stable residence (does not intend to move during the study period)
  • Not intending to quit smoking during the study period
  • Has a smart phone with a data plan (this study is being done remotely)
  • Saliva cotinine level >30 ng/mL

Exclusion Criteria:

  • Self-reported current pregnancy, currently trying to become pregnant, or breast-feeding
  • Current use of nicotine replacement products or cessation products (e.g., bupropion) or plans to use in the next 3 weeks for the purposes of cessation
  • Diagnosed with or being treated for COPD, emphysema, and/or uncontrolled asthma as determined by research screening
  • Currently taking anti-hypertensive medications
  • Currently has pneumonia, bronchitis, or COVID symptoms that has not yet resolved, or was hospitalized or visited the ER in the past 4 weeks for a respiratory-related illness that has not yet resolved (can be re-screened once resolved)

Sites / Locations

  • UConn HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Flavored Filtered Cigars

Unflavored Filtered Cigars

Arm Description

Half of the group will be randomized to start with flavored filtered cigars (FCs) at the second visit and cross over to unflavored FCs at the third visit. FCs will be Cheyenne filtered cigars.

Half of the group will be randomized to start with unflavored FCs at the second visit and cross over to flavored FCs at the third visit. FCs will be Cheyenne filtered cigars.

Outcomes

Primary Outcome Measures

Change in demand elasticity for preferred flavored filtered cigars
It is measured by the Cigarette Purchase Task, which will be adapted to assess these products. It is the hypothetical consumption of flavored cigars at increasing prices.
Change in demand elasticity for preferred unflavored filtered cigars
It is measured by the Cigarette Purchase Task, which will be adapted to assess these products. It is the hypothetical consumption of unflavored cigars at increasing prices.
Change in cross price elasticity for filtered cigars and cigarettes
It is measured by the Cross-Price Purchase Task. It is the hypothetical consumption of flavored and unflavored filtered cigars as cigarette prices increase.

Secondary Outcome Measures

Change in exhaled breath carbon monoxide (CO) level
Daily exhaled breath CO measured over the course of the study period

Full Information

First Posted
July 14, 2020
Last Updated
September 20, 2023
Sponsor
UConn Health
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT04487470
Brief Title
Impact of Cigar Flavor in Dual Users
Official Title
Impact of Cigar Flavor on Tobacco Use Behaviors and Addiction in Dual Users
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 24, 2020 (Actual)
Primary Completion Date
May 31, 2024 (Anticipated)
Study Completion Date
May 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UConn Health
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to understand addiction to filtered cigars (FCs) compared to cigarettes in young adults, ages 21-34, who smoke both cigarettes and cigars. We are also looking to see if flavors, such as fruit or menthol, make FCs more addictive and if there are differences between men and women. Participants will receive 2 weeks supply of FCs, one week flavored and another week unflavored. You will be randomized (like flipping a coin) to which type of FC you will receive first. The study will: take about 3-4 hours of your time per week over 3-5 weeks. be conducted remotely by phone, video call, email, and mail. require a smart phone to answer 5 quick surveys a day you will need to answer 4 weekly surveys take part in a weekly video or phone call with research staff supply three saliva samples to be later tested for nicotine and other toxicants and use a device to measure your carbon monoxide levels four times a day. You will be compensated for your time.
Detailed Description
The purpose of this remote study is to understand addiction to filtered cigars (FCs) compared to cigarettes in young adults, ages 21-34, who are dual users of cigarettes and cigars, if flavor, such as fruit or menthol, makes FCs more addictive, and if there are differences for men and women. The first hypothesis is that the potential for FCs to cause addiction will be lower than that of cigarettes but will increase as cigarette cost increases. Second, flavored FCs will be more addictive than unflavored FCs, and that the effect of flavored FCs on addiction will be greater in women than men. Last, participants will smoke more FCs and fewer cigarettes when given flavored compared to unflavored FCs. This study employs a crossover design (controlled for menthol status) in which 145 young adult dual users will be randomized to a flavored or unflavored FC that will be provided and then switch to the other type after 1 week. We will utilize the Cigarette Purchase Task, other standardized measures of dependence, and ecological momentary assessments to study the relationship between dependence indicators and smoking in the natural environment. Participation will take 3-4 hours of time per week over 3-5 weeks. Participants will be asked to complete brief surveys on their mobile phone 5 times a day, every day, weekly surveys about tobacco use, attitudes, and beliefs, and take part in a weekly video or phone call with research staff. They will need to use a carbon monoxide device we provide, four times a day, and provide 3 saliva samples that will later be analyzed for nicotine and other toxicants. All procedures will be conducted remotely by phone, computer, and mail.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Disorder
Keywords
Dual Tobacco Use, Smoking, Cigar Smoking, Cigarette Smoking

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Randomized cross-over study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
145 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Flavored Filtered Cigars
Arm Type
Experimental
Arm Description
Half of the group will be randomized to start with flavored filtered cigars (FCs) at the second visit and cross over to unflavored FCs at the third visit. FCs will be Cheyenne filtered cigars.
Arm Title
Unflavored Filtered Cigars
Arm Type
Experimental
Arm Description
Half of the group will be randomized to start with unflavored FCs at the second visit and cross over to flavored FCs at the third visit. FCs will be Cheyenne filtered cigars.
Intervention Type
Other
Intervention Name(s)
Flavored filtered cigars
Intervention Description
Flavored and unflavored Cheyenne filtered cigars that are currently available in the marketplace for purchase
Intervention Type
Other
Intervention Name(s)
Unflavored filtered cigars
Intervention Description
Flavored and unflavored Cheyenne filtered cigars that are currently available in the marketplace for purchase
Primary Outcome Measure Information:
Title
Change in demand elasticity for preferred flavored filtered cigars
Description
It is measured by the Cigarette Purchase Task, which will be adapted to assess these products. It is the hypothetical consumption of flavored cigars at increasing prices.
Time Frame
3-5 weeks
Title
Change in demand elasticity for preferred unflavored filtered cigars
Description
It is measured by the Cigarette Purchase Task, which will be adapted to assess these products. It is the hypothetical consumption of unflavored cigars at increasing prices.
Time Frame
3-5 weeks
Title
Change in cross price elasticity for filtered cigars and cigarettes
Description
It is measured by the Cross-Price Purchase Task. It is the hypothetical consumption of flavored and unflavored filtered cigars as cigarette prices increase.
Time Frame
3-5 weeks
Secondary Outcome Measure Information:
Title
Change in exhaled breath carbon monoxide (CO) level
Description
Daily exhaled breath CO measured over the course of the study period
Time Frame
3-5 weeks
Other Pre-specified Outcome Measures:
Title
Change in saliva cotinine levels
Description
Saliva samples will be analyzed for cotinine levels
Time Frame
3-5 weeks
Title
Change in number of flavored cigars, unflavored cigars, and cigarettes smoked per day
Description
Participants will record tobacco use daily on their mobile phones using an app.
Time Frame
3-5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
34 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Current regular dual uses of filtered cigars and cigarillos (FCs) and cigarettes defined as; (a) report smoking cigarettes at least weekly in the past 30 days, (b) report smoking unaltered FC (without marijuana) at least weekly in the past 30 days; and (c)report cigarette and cigar use at their current rate (or more frequently) for ≥ 3 months. Able to read, speak, and understand English Age 21-34 years Stable residence (does not intend to move during the study period) Not intending to quit smoking during the study period Has a smart phone with a data plan (this study is being done remotely) Saliva cotinine level >30 ng/mL Exclusion Criteria: Self-reported current pregnancy, currently trying to become pregnant, or breast-feeding Current use of nicotine replacement products or cessation products (e.g., bupropion) or plans to use in the next 3 weeks for the purposes of cessation. Diagnosed with or being treated for COPD, emphysema, and/or uncontrolled asthma as determined by research screening. Currently taking anti-hypertensive medications Currently has pneumonia, bronchitis, or COVID symptoms that has not yet resolved, or was hospitalized or visited the ER in the past 4 weeks for a respiratory-related illness that has not yet resolved (can be re-screened once resolved) Resident of Alaska, Hawaii, or Massachusetts
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adam Flores, RA 1
Phone
(860)305-3061
Email
adflores@uchc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine Jahne, BSN, RN, RA 3
Phone
(860)679-1138
Email
jahne@uchc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erin Mead-Morse, PhD,MHS
Organizational Affiliation
UConn Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
UConn Health
City
Farmington
State/Province
Connecticut
ZIP/Postal Code
06030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adam Flores, BS
Phone
860-305-3061
Email
adflores@uchc.edu
First Name & Middle Initial & Last Name & Degree
Erin L Mead-Morse, PhD,MHS
Phone
860-679-2456
Email
mead@uchc.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
A verified database will be available once the main findings from the final dataset have been reported and accepted for publication. Information that does result from our analysis of the saliva samples will be available after publication of the findings. De-identified dataset will contain the data merged from all study visits. We will include with the data file proper documentation of all data (including definitions of variables and derived variables, frequencies, details about codes, etc.), and procedures used to collect the data, to ensure others can use the dataset and to prevent misuse, misinterpretation, and/or confusion. The database intended for public distribution will be free of identifiers that would permit linkages to individual research participants and variables that could lead to deductive disclosure of the identity of individual subjects.
IPD Sharing Time Frame
In the final year of the Award after the dataset is finalized we will prepare a file in Excel and Stata that contains all study variables intended for use in presentations and publications.

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Impact of Cigar Flavor in Dual Users

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