MedPath

Low Nicotine Content Cigarettes in Vulnerable Populations: Affective Disorders

Phase 2
Completed
Conditions
Tobacco Use Disorder
Interventions
Other: Either normal nicotine content cigarettes (15.8mg/g) or reduced nicotine content cigarettes (0.4mg/g)
Other: E-Cigarettes
Registration Number
NCT04090879
Lead Sponsor
Brown University
Brief Summary

While the prevalence of smoking in the United States general population has declined over the past 50 years, there has been little to no decline among people with mental health conditions. Affective Disorders (ADs) are the most common mental health conditions in the US, and over 40% of people with ADs are current smokers. A national policy of reducing the nicotine content of cigarettes has the potential to reduce tobacco use, dependence, and related adverse health outcomes. Controlled trials in psychiatrically-stable smokers have shown that reducing the nicotine content in cigarettes can reduce cigarettes per day (CPD), dependence and tobacco toxicant exposure, with few adverse consequences.

The goal of the proposed trial is to experimentally model whether increasing the availability and appeal of an alternative, non-combusted source of nicotine (e-cigarettes) moderates the effect of altering the nicotine in cigarettes in smokers with ADs. Additionally, investigators will test whether allowing participants to personalize the flavor of the e-liquid alters any moderating effects their availability may have on tobacco cigarette smoking.

Daily smokers with current ADs will be recruited at Brown University and the University of Vermont.

Investigators will study two research cigarettes referred to here as Research Cigarette 1 (RC1) and Research Cigarette 2 (RC2). One of these cigarettes will be a normal nicotine content cigarette and the other will be a reduced nicotine content cigarette. Investigators will study two e-cigarette conditions referred to here as E-Cigarette Condition 1 (EC1) and E-Cigarette Condition 2 (EC2). Both e-cigarette conditions will involve the same commercially available devices and same nicotine-containing e-liquid, but in one condition that e-liquid will be available only in tobacco flavor while in the other condition that e-liquid will be available in multiple flavors from which participants can choose based on personal taste preference. Participants will be assigned to one of the following four study conditions: (1) RC1 only; (2) RC2 only; (3) RC2 + EC1; (4) RC2 + EC2.

Participants will be asked to use only their assigned study products for 16 weeks. Outcome measures include total CPD, cigarette demand assessed by behavioral economics-based purchase tasks, craving, withdrawal, psychiatric symptoms, breath carbon monoxide (CO), biomarkers of tobacco toxicant exposure, brain function and structure, and airway inflammation (fractional nitric oxide concentration in exhaled breath \[FeNO\]).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
326
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RC 2 + EC 2Either normal nicotine content cigarettes (15.8mg/g) or reduced nicotine content cigarettes (0.4mg/g)Research Cigarettes #2 plus E-cigarettes #2 (participants can choose among varying flavors)
RC 2 + EC 2E-CigarettesResearch Cigarettes #2 plus E-cigarettes #2 (participants can choose among varying flavors)
RC 2 + EC 1Either normal nicotine content cigarettes (15.8mg/g) or reduced nicotine content cigarettes (0.4mg/g)Research Cigarettes #2 plus E-cigarettes #1 (participants receive tobacco flavor only)
RC 2 + EC 1E-CigarettesResearch Cigarettes #2 plus E-cigarettes #1 (participants receive tobacco flavor only)
RC 1 onlyEither normal nicotine content cigarettes (15.8mg/g) or reduced nicotine content cigarettes (0.4mg/g)Research Cigarettes #1
RC 2 onlyEither normal nicotine content cigarettes (15.8mg/g) or reduced nicotine content cigarettes (0.4mg/g)Research Cigarettes #2
Primary Outcome Measures
NameTimeMethod
Cigarettes Per Day16 weeks

Cigarettes per day will be assessed for use of cigarettes with different nicotine content.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

University of Vermont

🇺🇸

Burlington, Vermont, United States

Brown University

🇺🇸

Providence, Rhode Island, United States

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