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Flavored vs Unflavored Cigars for Tobacco Use Disorder
N/A
Recruiting
Led By Erin Mead-Morse, PhD,MHS
Research Sponsored by UConn Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age 18-34 years
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-5 weeks
Awards & highlights
Study Summary
This trial is studying whether filtered cigars are more addictive than cigarettes, if flavor makes filtered cigars more addictive, and if there are differences for men and women.
Who is the study for?
This study is for young adults aged 18-34 who regularly smoke both cigarettes and filtered cigars, are not planning to quit soon, and have a stable living situation. Participants must be able to use a smartphone with data for surveys and video calls, understand English, and not be pregnant or breastfeeding.Check my eligibility
What is being tested?
The trial aims to compare the addictiveness of flavored versus unflavored filtered cigars in dual smokers (cigarettes and cigars). Over 3-5 weeks, participants will try each type for one week while providing saliva samples, completing surveys multiple times daily, and measuring their carbon monoxide levels.See study design
What are the potential side effects?
While specific side effects are not listed for trying flavored or unflavored cigars, potential risks include increased nicotine addiction and exposure to harmful substances found in tobacco products.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 34 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-5 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-5 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in cross price elasticity for filtered cigars and cigarettes
Change in demand elasticity for preferred flavored filtered cigars
Change in demand elasticity for preferred unflavored filtered cigars
Secondary outcome measures
Change in exhaled breath carbon monoxide (CO) level
Other outcome measures
Change in number of flavored cigars, unflavored cigars, and cigarettes smoked per day
Change in saliva cotinine levels
Trial Design
2Treatment groups
Experimental Treatment
Group I: Unflavored Filtered CigarsExperimental Treatment1 Intervention
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.
Group II: Flavored Filtered CigarsExperimental Treatment1 Intervention
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.
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Who is running the clinical trial?
UConn HealthLead Sponsor
211 Previous Clinical Trials
60,476 Total Patients Enrolled
9 Trials studying Tobacco Use Disorder
1,238 Patients Enrolled for Tobacco Use Disorder
National Institute on Drug Abuse (NIDA)NIH
2,497 Previous Clinical Trials
2,623,678 Total Patients Enrolled
272 Trials studying Tobacco Use Disorder
48,880 Patients Enrolled for Tobacco Use Disorder
Erin Mead-Morse, PhD,MHSPrincipal Investigator - UConn Health
UConn Health
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been diagnosed with or am being treated for COPD, emphysema, or uncontrolled asthma.I am using or plan to use nicotine replacement or cessation products soon.I am currently on medication for high blood pressure.You plan to continue smoking during the study.I currently have or recently had a serious respiratory illness.I am between 18 and 34 years old.I have been regularly smoking both cigarettes and cigars for at least 3 months.
Research Study Groups:
This trial has the following groups:- Group 1: Flavored Filtered Cigars
- Group 2: Unflavored Filtered Cigars
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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