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Evaluation of Very Low Nicotine Content Cigarettes in Adolescent Smokers

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Brown University

Status

Completed

Conditions

Nicotine Dependence

Treatments

Other: Standard nicotine content cigarettes
Other: Very low nicotine content cigarettes

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02587312
1K01CA189300

Details and patient eligibility

About

The purpose of this study is to determine how reducing the level of nicotine in cigarettes may affect adolescent smoking behavior. In this study, the researchers will randomize adolescent (age 15-19) daily smokers to either receive VLNC cigarettes or normal-nicotine content (NNC) study cigarettes for three weeks following a one-week usual-brand baseline period. Participants will be instructed to smoke only those cigarettes. The researchers will conduct daily assessments of total cigarette use (both study cigarette and non-compliant use of usual brand cigarettes), craving, and withdrawal, weekly assessments of breath carbon monoxide (CO) levels, cigarette acceptability, risk perceptions of VLNC and NNC cigarettes and demand for usual-brand cigarettes, and pre- vs. post-use measures of nicotine and toxicant exposure. Overall, the project will help determine how VLNC cigarettes may affect real-world smoking behavior in adolescents, and illuminate the potential mechanisms through which these products may effect such changes. Such knowledge will contribute to the science base that may inform future policy decisions.

Enrollment

70 patients

Sex

All

Ages

15 to 19 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • current daily smoking (1 or more cigarettes per day for the past 6 months or longer). Participants must meet a breath carbon monoxide criterion of 6 ppm or higher; if this is not met, urine cotinine levels, detected by a NicAlert cotinine screening device, must indicate recent smoking (level 3 or higher).
  • Participants must speak and comprehend English well enough to complete study procedures.

Exclusion criteria

  • Current pregnancy
  • Self-reported daily use of alcohol or other non-prescribed drugs (excluding marijuana).
  • Participants who are seeking treatment for their smoking or who report that they intend to quit smoking within the next 30 days and have made a 24-hour quit attempt in the past year
  • Participants who report current suicidal ideation on the MINI suicide subscale questions 4 & 5 ("In the past month did you have a suicide plan?" and "In the past month did you attempt suicide?"), as well as participants who indicate that they have made a suicide attempt in their lifetime
  • Participants who report use of other non-cigarette tobacco products more than 9 out of the last 30 days

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

70 participants in 2 patient groups

Normal Nicotine Content Cigarettes
Active Comparator group
Description:
SPECTRUM cigarette: 0.8 mg nicotine with 10.5 mg tar (standard nicotine and tar yields of commercially available cigarettes; control condition)
Treatment:
Other: Standard nicotine content cigarettes
Very Low Nicotine Content Cigarettes
Experimental group
Description:
SPECTRUM cigarette: 0.03 mg nicotine with 9 mg tar
Treatment:
Other: Very low nicotine content cigarettes

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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