Manipulating E-Cigarette Nicotine to Promote Public Health
May 8, 2026 updated by: Theodore Wagener, Ohio State University Comprehensive Cancer Center
This clinical trial explores the manipulation of e-cigarette (EC) nicotine to promote public health.
Researchers are trying to understand and gather information about how the strength, form, and structure of nicotine in products play a significant role in their potential for addiction and how they might affect health risks.
The information gained from this study may allow researchers to understand how these aspects of nicotine influence the potential for addiction, how people puff on ECs, how the body processes nicotine, and any potential harmful effects it might have on health.
Exploring these specific characteristics of nicotine may also determine if an EC product standard could help identify optimal nicotine levels for users.
Study Overview
Status
Recruiting
Conditions
Detailed Description
PRIMARY OBJECTIVES:
I. Assess the pharmacological, metabolic, and behavioral impact of nicotine dimensions. (Study 1) II. Assess the toxicity resulting from different nicotine dimension combinations. (Study 1) III. Across ecologically valid nicotine concentrations and isomer ratios, determine free-base (FB) nicotine fractions with minimal appeal to young adult EC users but sufficient appeal to smokers. (Study 2)
OUTLINE:
Phase 1 (STUDY 1): Participants are randomized to the order of 8 e-liquid combinations varying in nicotine concentration, form, and isomer.
Participants participate in a 10-puff vaping session over 5 minutes with a study e-liquid using the study EC device followed by a 60 minute washout period and then an ad libitum puffing session over 60 minutes at each lab visit. Patients are also given a new pre-filled study device corresponding to the study e-liquid they will use for the subsequent visit to practice at home. Puffing sessions continue with a new study e-liquid at each of the 8 lab visits lasting up to 4 hours each. Participants also undergo carbon monoxide (CO) testing and blood and urine sample collection on study.
Phase 2 (STUDY 2): Participants are randomized to the order of 20 e-liquid combinations varying in concentration, FB fractions, and isomer.
Participants will take part in a 2-puff vaping session with each of the 20 study e-liquids using the study EC device with a 20-minute washout period between each vaping session. Vaping sessions are grouped into two visits, each lasting up to 5 hours and consisting of 10 e-liquids. Participants also undergo CO testing and blood and urine sample collection on study.
Study Type
Interventional
Enrollment (Estimated)
375
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ohio
-
Columbus, Ohio, United States, 43210
- Recruiting
- Ohio State University Comprehensive Cancer Center
-
Principal Investigator:
- Theodore L. Wagener, PhD
-
Contact:
- Theodore L. Wagener, PhD
- Phone Number: 844-744-2447
- Email: ccc-tobacco@osumc.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Current exclusive young adult EC user for at least the past 3 months (confirmed by cotinine testing strip) between 21-24 years old with no/minimal history of smoking cigarettes (≤ 10 cigarettes in entire life)
- Current older adult smoker (daily use, ≥ 100 cigarettes in entire life) aged 25-65 with interest in trying an EC
- Willing to abstain from all nicotine, tobacco products, and marijuana for at least 12 hours for Study 1 and 2 hours for Study 2 before study visits
- Read, write, and speak English
Exclusion Criteria:
- Currently attempting to quit nicotine or tobacco products
- Currently pregnant (will be verified with urine pregnancy test), planning to become pregnant, or breastfeeding
- If age 21-24 years old AND use of any tobacco products other than ECs (use of >10 cigarettes in entire life; use of >10 traditional cigars, cigarillos, or filtered cigars in entire life; use of smokeless tobacco products >10 times in entire life; or hookah in the last 30 days).
- Self-reported diagnosis of lung disease including asthma, cystic fibrosis, or chronic obstructive pulmonary disease
- New or unstable cardiovascular disease diagnosed within the past 3 months
- Use of medications that are inducers of CYP2A6 enzyme such as rifampicin, dexamethasone, phenobarbital, and other anti-convulsion drugs
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Phase 1, Arm 1 (High, Nic, S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 2 (High, Nic, R/S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 3 (Low, Nic, S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 4 (Low, Nic, R/S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 5 (High, NicH+, S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 6 (High, NicH+, R/S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 7 (Low, NicH+, S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 1, Arm 8 (Low, NicH+, R/S)
Participants are randomized to vape one out of the eight study e-liquids in a 10-puff vaping session over 5 minutes using the e-cig study device and then in an ad libitum puffing session over 60 minutes.
The 8 e-liquids vary in nicotine concentration (low [20 mg/g] or high [50 mg/g]), form (Nic or NicH+), and isomer (S-nicotine or R/S nicotine).
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 1 (High, 5%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 2 (High, 5%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 3 (Low, 5%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 4 (Low, 5%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 5 (High, 25%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 6 (High, 25%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 7 (Low, 25%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 8 (Low, 25%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 9 (High, 45%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 10 (High, 45%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 11 (Low, 45%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 12 (Low, 45%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 13 (High , 65%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 14 (High , 65%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 15 (Low, 65%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 16 (Low, 65%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 17 (High, 85%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 18 (High, 85%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 19 (Low, 85%, S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
|
Experimental: Phase 2, Arm 20 (Low, 85%, R/S)
Participants vape 20 different study e-liquids varying in concentration (low [20 mg/g] or high [50 mg/g]), freebase nicotine percentage (5%, 25%, 45%, 65%, or 85%), and isomer (S-nicotine or R/S nicotine) using the e-cig study device during two visits.
|
Ancillary studies
Undergo blood and urine sample collection
Other Names:
Undergo CO test
Other Names:
Sample study e-liquids in vaping sessions at research lab with e-cig study device
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nicotine pharmacokinetics: Maximum nicotine blood level (Cmax) (Study 1)
Time Frame: Immediately before puffing (-5 minutes), and at 5, 15, 60, and 120 minutes after the start of the puffing session
|
Blood nicotine samples will be assayed using liquid chromatography tandem mass spectrometry (LC-MS/MS) with deuterated internal standards.
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Immediately before puffing (-5 minutes), and at 5, 15, 60, and 120 minutes after the start of the puffing session
|
|
Nicotine pharmacokinetics: Time to maximum blood level (Tmax) (Study 1)
Time Frame: Immediately before puffing (-5 minutes), and at 5, 15, 60, and 120 minutes after the start of the puffing session
|
Blood nicotine samples will be assayed using LC-MS/MS with deuterated internal standards.
|
Immediately before puffing (-5 minutes), and at 5, 15, 60, and 120 minutes after the start of the puffing session
|
|
Nicotine pharmacokinetics: Area under the curve (AUC) (Study 1)
Time Frame: Immediately before puffing (-5 minutes), and at 5, 15, 60, and 120 minutes after the start of the puffing session
|
Blood nicotine samples will be assayed using LC-MS/MS with deuterated internal standards.
|
Immediately before puffing (-5 minutes), and at 5, 15, 60, and 120 minutes after the start of the puffing session
|
|
Nicotine metabolism (Study 1)
Time Frame: At 60 minutes after the start of each puffing session
|
The rate of nicotine metabolism will be assessed using the standard method of nicotine metabolite ration (NMR) = hydroxycotinine/cotinine, modified to reflect stereoselective metabolism.
Plasma concentration of cotinine, and hydroxycotinine will be measured by chiral LC-MS/MS based on previous methods and quantified using the ratio of metabolites to internal standards.
|
At 60 minutes after the start of each puffing session
|
|
Reactive oxygen species (ROS) (Study 1)
Time Frame: Up to 2 years
|
The recorded puffing topographies will be sent to the analytical lab for "puff playback" generation of EC aerosols and quantification of ROS.
We will use an acellular ROS assay previously developed by our team as a generic toxicity assessment method.
|
Up to 2 years
|
|
Nicotine toxicity measures (Study 1)
Time Frame: Up to 2 years
|
Will be assessed by carbonyl yields reported as ug/session or ug/puff or normalized per nicotine yield for a head-to-head comparison between different nicotine conditions.
|
Up to 2 years
|
|
In vitro nicotine toxicity measures: Cell cycle and proliferation (Study 1)
Time Frame: Up to 2 years
|
Will be assessed by cell cycle and proliferationg.
|
Up to 2 years
|
|
In vitro nicotine toxicity measures: Cytotoxicity (Study 1)
Time Frame: Up to 2 years
|
Will be assessed by cytotoxicity, senescence.
|
Up to 2 years
|
|
In vitro nicotine toxicity measures: Senescence (Study 1)
Time Frame: Up to 2 years
|
Will be assessed by senescence.
|
Up to 2 years
|
|
In vitro nicotine toxicity measures: RNA sequencing (Study 1)
Time Frame: Up to 2 years
|
Will be assessed by RNA sequencing.
|
Up to 2 years
|
|
Nicotine yield (Study 1)
Time Frame: Up to 2 years
|
Using a dilute-and-shoot method developed by our team, nicotine yield in EC aerosol will be quantified using the "playback" technique (i.e., use topography collected from participants to machine-generate EC aerosols) and GC-MS method, developed by our group to minimize the PG/VG interference not addressed by other methods.
|
Up to 2 years
|
|
Modified Cigarette Evaluation Questionnaire (mCEQ)(Study 1)
Time Frame: Study visits 2 through 9
|
The modified Cigarette Evaluation Questionnaire (mCEQ) will assess subjective responses.
The 11-item mCEQ includes five subscales: Smoking Satisfaction, Psychological Reward, Aversion, Enjoyment of Respiratory Tract Sensations, and Craving Reduction, with items rated from 1 (not at all) to 7 (extremely likely).
Items are averaged to create each of the subscales also ranging from 1 to 7 with higher values indicating greater levels of smoking satisfaction, psychological reward, aversion, enjoyment of respiratory tract sensations, and craving reduction.
|
Study visits 2 through 9
|
|
Tiffany-Drobes Questionnaire of Smoking Urges: Brief Form (QSU)
Time Frame: Study visits 2 through 9
|
Smoking and vaping urges/craving will be measured using the Tiffany-Drobes Questionnaire of Smoking Urges: Brief Form with a modified version (replacing the word "cigarette" with "e-cigarette") for EC users.
This is a 10-item measure where participants rate smoking/vaping-related items on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree).
Similar to previous studies, we will collapse the items into two previously identified factors (Factor 1: strong desire and intention to smoke/vape; Factor 2: anticipation of relief from withdrawal symptoms).
Scores are calculated by summing the items and range from 5 to 35 for each of the factors with higher scores indicating greater craving to smoke/vape.
|
Study visits 2 through 9
|
|
Drug Effects/Liking Questionnaire (DEQ)(Study 1)
Time Frame: Study visits 2 through 9
|
Assess the desire and liking of products, positive and negative effects (i.e., side effects), and perceived strength and effectiveness.
Scores range from 1 to 5 with higher scores indicating greater strength (effect from smoking cigarettes/vaping e-cigarettes) or liking (liking of effect from smoking cigarettes/vaping e-cigarettes)
|
Study visits 2 through 9
|
|
Minnesota Nicotine Withdrawal Scale (MNWS)(Study 1)
Time Frame: Study visits 2 through 9
|
Asses Nicotine withdrawal and smoking craving, anger/irritability, anxiety, depressed mood, restlessness/difficulty concentrating, increased appetite, sleep problems, and somatic symptoms (nausea, constipation, sore throat, dizziness, coughing).
Scores range from 0 to 4 with higher scores indicating greater levels of withdrawal (MNWS) or more craving to smoke (MNWS Craving).
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Study visits 2 through 9
|
|
Puffing topography: Puff count (Study1)
Time Frame: 60 minute puffing session at each of the 8 study lab visits
|
Puff count will be measured.
|
60 minute puffing session at each of the 8 study lab visits
|
|
Puffing topography: Average puff duration (Study1)
Time Frame: 60 minute puffing session at each of the 8 study lab visits
|
Average puff duration will be measured.
|
60 minute puffing session at each of the 8 study lab visits
|
|
Puffing topography: inter-puff interval (Study1)
Time Frame: 60 minute puffing session at each of the 8 study lab visits
|
Inter-puff interval will be measured.
|
60 minute puffing session at each of the 8 study lab visits
|
|
Puffing topography: Flow rate (Study1)
Time Frame: 60 minute puffing session at each of the 8 study lab visits
|
Flow rate will be measured.
|
60 minute puffing session at each of the 8 study lab visits
|
|
Puffing topography: Volume (Study1)
Time Frame: 60 minute puffing session at each of the 8 study lab visits
|
Puff volume will be measured.
|
60 minute puffing session at each of the 8 study lab visits
|
|
General Labeled Magnitude Scale (gLMS) (Study 2)
Time Frame: 1 six hour lab visit
|
Complete the General Labeled Magnitude Scale (gLMS) after each condition.
Scores range from 0 "No Sensation" to 100 "Strongest Imaginable".
|
1 six hour lab visit
|
|
Labeled Hedonic Scale (LHS) (Study 2)
Time Frame: 1 six hour lab visit
|
Complete the Labeled Hedonic Scale (LHS) after each condition.
Scores range from -100 "Most Disliked Imaginable" to 100 "Most Liked Imaginable".
|
1 six hour lab visit
|
|
Sensory Attributes (Study 2)
Time Frame: 1 six hour lab visit
|
Rate sensory attributes (smoothness, harshness, sweetness, bitterness) on a 100-unit visual analog scale after each condition.
|
1 six hour lab visit
|
|
Overall acceptance: Industry-designed Thermometer Rating Scale (Study 2)
Time Frame: 1 six hour lab visit
|
Complete a tobacco industry-designed thermometer rating scale of overall acceptance after each condition.
Ratings range from 0 "the very worst" to 100 "the very best", with 50 indicating "indifferent".
|
1 six hour lab visit
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Theodore L Wagener, Ohio State University Comprehensive Cancer Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 20, 2024
Primary Completion (Estimated)
May 20, 2027
Study Completion (Estimated)
May 20, 2027
Study Registration Dates
First Submitted
May 22, 2024
First Submitted That Met QC Criteria
June 3, 2024
First Posted (Actual)
June 7, 2024
Study Record Updates
Last Update Posted (Actual)
May 13, 2026
Last Update Submitted That Met QC Criteria
May 8, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OSU-23143
- NCI-2023-05712 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
Yes
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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