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Behavioural Intervention

E-Cigarette Flavors for Vaping Effects

N/A
Recruiting
Led By Caroline O Cobb, PhD
Research Sponsored by Virginia Commonwealth University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 55 minutes (session 1) and up to 120 minutes (sessions 2-4) into the session
Awards & highlights

Study Summary

This trial will test how nicotine levels and flavors in e-cigarettes affect abuse liability indices in current smokers.

Who is the study for?
This trial is for healthy adult smokers who use cigarettes at least three days a week, with at least one cigarette per day. Participants must be willing to give informed consent and attend lab sessions. Pregnant or breastfeeding women cannot join. More eligibility details will be shared after the study ends.Check my eligibility
What is being tested?
The study is examining if different flavors and nicotine levels in e-cigarettes affect how likely people are to keep using them compared to their own brand of cigarettes. It involves comparing tobacco-flavored e-cigarettes with varying nicotine delivery against regular cigarettes and testing menthol flavor's influence.See study design
What are the potential side effects?
Potential side effects may include typical reactions associated with nicotine products such as dizziness, dry mouth, throat irritation, or increased heart rate. Specific side effects related to this trial have not been detailed but can align with common e-cigarette use.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 55 minutes (session 1) and up to 120 minutes (sessions 2-4) into the session
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 55 minutes (session 1) and up to 120 minutes (sessions 2-4) into the session for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Breakpoint of Drug Purchase Task (DPT)
Cross-price elasticity of the Cross Product-DPT
Elasticity of Drug Purchase Task (DPT)
+3 more
Other outcome measures
Change in Heart Rate
General Labeled Magnitude Scale
Labeled Hedonic Scale
+3 more

Trial Design

7Treatment groups
Experimental Treatment
Active Control
Group I: NJOY Daily 6.0% nicotine ECIG - Menthol flavorExperimental Treatment1 Intervention
Group II: NJOY Daily 6.0% nicotine ECIG - Extra Rich Tobacco flavorExperimental Treatment1 Intervention
Group III: NJOY Ace 5.0% nicotine ECIG - Menthol flavorExperimental Treatment1 Intervention
Group IV: NJOY Ace 5.0% nicotine ECIG - Classic Tobacco flavorExperimental Treatment1 Intervention
Group V: NJOY Ace 2.4% nicotine ECIG - Menthol flavorExperimental Treatment1 Intervention
Group VI: NJOY Ace 2.4% nicotine ECIG - Classic Tobacco flavorExperimental Treatment1 Intervention
Group VII: Own Brand CigaretteActive Control1 Intervention

Find a Location

Who is running the clinical trial?

Virginia Commonwealth UniversityLead Sponsor
699 Previous Clinical Trials
22,885,009 Total Patients Enrolled
National Institute on Drug Abuse (NIDA)NIH
2,470 Previous Clinical Trials
2,619,695 Total Patients Enrolled
10 Trials studying Vaping
5,072 Patients Enrolled for Vaping
Caroline O Cobb, PhDPrincipal InvestigatorVirginia Commonwealth University
2 Previous Clinical Trials
242 Total Patients Enrolled

Media Library

Tobacco product administration and assessment (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05971823 — N/A
Vaping Research Study Groups: NJOY Ace 2.4% nicotine ECIG - Menthol flavor, NJOY Ace 5.0% nicotine ECIG - Menthol flavor, Own Brand Cigarette, NJOY Ace 2.4% nicotine ECIG - Classic Tobacco flavor, NJOY Ace 5.0% nicotine ECIG - Classic Tobacco flavor, NJOY Daily 6.0% nicotine ECIG - Menthol flavor, NJOY Daily 6.0% nicotine ECIG - Extra Rich Tobacco flavor
Vaping Clinical Trial 2023: Tobacco product administration and assessment Highlights & Side Effects. Trial Name: NCT05971823 — N/A
Tobacco product administration and assessment (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05971823 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Do I qualify to participate in this research endeavor?

"Eligibility for entry into this study is restricted to candidates that have vaped in the past and are aged between 18-55. The trial aims to accrue 36 participants."

Answered by AI

Is geriatric participation acceptable for this clinical experiment?

"This trial is open to participants aged between 18 and 55 years old. Patients younger than 18 or older than 65 can look into 1 or 3 alternative studies, respectively."

Answered by AI

Is the research team currently recruiting participants for this experiment?

"According to records on clinicaltrials.gov, this research project is not currently recruiting participants. The trial was first posted on August 1st 2023 and the most recent edit made was July 31st 2023; however there are 12 additional studies that presently require volunteers."

Answered by AI
~9 spots leftby Aug 2024