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Reduced Nicotine Content Cigarettes and Tobacco Switching Behaviors

Primary Purpose

Tobacco Addiction, Dual Tobacco Use

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
VLNC cigarettes
Combusted Products
Non-combusted products
CN cigarettes
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Tobacco Addiction focused on measuring Cigarette Smoking, Very Low Nicotine Content cigarettes (VLNC), Dual Tobacco Use

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Male or female subjects who are at least 18 years of age with a history of regular smoking for at least 1 year and no serious quit attempts in the last 3 months
  • No unstable and significant medical or psychiatric conditions, including lack of stabilization of medications.
  • Subject has provided written informed consent to participate in the study

Exclusion Criteria:

  • Regular use of tobacco products (including e-cigarettes) other than cigarettes
  • Regular use of nicotine replacement or other tobacco cessation products for purpose of quitting.
  • Pregnant or breastfeeding (due to toxic effects from tobacco products).
  • Planned quit date within the next two months.
  • Does not have a way that the research team can communicate with them by phone or e-mail.
  • Not able to read and write English well enough to complete study activities without translation.

Sites / Locations

  • University of Minnesota Tobacco Research Program

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

CN + combusted & non-combusted products

VLNC + combusted & non-combusted products

VLNC with non-combusted products

Arm Description

Subjects will be asked to smoke the assigned conventional nicotine content (CN) cigarettes, instead of their normal brand, for 8 weeks and will also be given access to use other combusted and non-combusted tobacco and medicinal nicotine products during that time.

Subjects will be asked to smoke the assigned very low nicotine content (VLNC) cigarettes, instead of their normal brand, for 8 weeks and will also be given access to use other combusted and non-combusted tobacco and medicinal nicotine products during that time.

Subjects will be asked to smoke very low nicotine content (VLNC) cigarettes instead of their usual cigarettes for an 8 week period and will be given the opportunity to use non-combusted types of tobacco and medicinal tobacco products.

Outcomes

Primary Outcome Measures

Number of Days Using Alternative Products
The primary aim of the study is to determine the rate of use of alternative nicotine-containing products across the three experimental conditions.
Number of Combusted Products Smoked
Number of combusted products smoked per day during the last two weeks of the intervention period.

Secondary Outcome Measures

Rate of 24 Hour Quit Attempts
Rate of 24 hour quit attempts during the intervention period
Carcinogen Exposure Biomarker: Total NNAL
Total NNAL (pmol/mg creatinine) is a measure of carcinogen exposure assessed at the end of intervention.

Full Information

First Posted
November 27, 2013
Last Updated
February 14, 2017
Sponsor
University of Minnesota
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT02000921
Brief Title
Reduced Nicotine Content Cigarettes and Tobacco Switching Behaviors
Official Title
Models for Tobacco Productive Evaluation: Reduced Nicotine Content Cigarettes and Tobacco Switching Behaviors
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The main focus of this study is to determine the use of nicotine-containing products across the three experimental conditions. Subjects will be monitored to determine their continued use of assigned cigarettes, switching to other combusted and/or non-combusted tobacco, or cessation of all tobacco containing products.
Detailed Description
This is a single site, single-blind, randomized trial with three experimental conditions tested for a period of 8 weeks: 1) Very low nicotine content (VLNC) cigarettes (0.07 nicotine yield) with access to combusted (except cigarettes) and non-combusted tobacco and medicinal nicotine products; 2) VLNC cigarettes with access to only non-combusted tobacco and medicinal nicotine products; and 3) conventional nicotine (CN) content experimental cigarettes (0.8 mg nicotine) with access to combusted and non-combusted products. This study will examine the use of nicotine-containing products across the three experimental conditions. Subjects will be monitored to determine their continued use of assigned cigarettes, switching to other combusted (e.g., little cigars, large cigars, pipes) and/or non-combusted tobacco products (e.g., conventional smokeless tobacco, snus for smokers, dissolvables, e-cigarettes, medicinal nicotine), or cessation of all tobacco containing products. Toxicant exposure across the three conditions will also be examined. Eligible subjects will be provided very low nicotine content cigarettes and are told to use the product ad lib for 8 weeks. Subjects will complete questionnaires on demographics, smoking and health history, drug and alcohol use history, mood and perceptions of the study tobacco product. Biomarker samples will be analyzed for exposure levels of nicotine and tobacco-related toxicants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Addiction, Dual Tobacco Use
Keywords
Cigarette Smoking, Very Low Nicotine Content cigarettes (VLNC), Dual Tobacco Use

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
136 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CN + combusted & non-combusted products
Arm Type
Experimental
Arm Description
Subjects will be asked to smoke the assigned conventional nicotine content (CN) cigarettes, instead of their normal brand, for 8 weeks and will also be given access to use other combusted and non-combusted tobacco and medicinal nicotine products during that time.
Arm Title
VLNC + combusted & non-combusted products
Arm Type
Experimental
Arm Description
Subjects will be asked to smoke the assigned very low nicotine content (VLNC) cigarettes, instead of their normal brand, for 8 weeks and will also be given access to use other combusted and non-combusted tobacco and medicinal nicotine products during that time.
Arm Title
VLNC with non-combusted products
Arm Type
Experimental
Arm Description
Subjects will be asked to smoke very low nicotine content (VLNC) cigarettes instead of their usual cigarettes for an 8 week period and will be given the opportunity to use non-combusted types of tobacco and medicinal tobacco products.
Intervention Type
Other
Intervention Name(s)
VLNC cigarettes
Other Intervention Name(s)
Very Low Nicotine Content Cigarettes
Intervention Description
Modified risk tobacco product
Intervention Type
Other
Intervention Name(s)
Combusted Products
Intervention Description
Options for combusted tobacco products include cigars, cigarillos, and little cigars, .
Intervention Type
Other
Intervention Name(s)
Non-combusted products
Intervention Description
Options for non-combusted tobacco products include smokeless tobacco, novel snus products, e-cigarettes and medicinal nicotine.
Intervention Type
Other
Intervention Name(s)
CN cigarettes
Intervention Description
Experimental cigarettes with conventional nicotine content.
Primary Outcome Measure Information:
Title
Number of Days Using Alternative Products
Description
The primary aim of the study is to determine the rate of use of alternative nicotine-containing products across the three experimental conditions.
Time Frame
8 week intervetnion period
Title
Number of Combusted Products Smoked
Description
Number of combusted products smoked per day during the last two weeks of the intervention period.
Time Frame
At weeks 6-8 (last two weeks of intervention period)
Secondary Outcome Measure Information:
Title
Rate of 24 Hour Quit Attempts
Description
Rate of 24 hour quit attempts during the intervention period
Time Frame
8 week intervention period
Title
Carcinogen Exposure Biomarker: Total NNAL
Description
Total NNAL (pmol/mg creatinine) is a measure of carcinogen exposure assessed at the end of intervention.
Time Frame
Week 8 (end of intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or female subjects who are at least 18 years of age with a history of regular smoking for at least 1 year and no serious quit attempts in the last 3 months No unstable and significant medical or psychiatric conditions, including lack of stabilization of medications. Subject has provided written informed consent to participate in the study Exclusion Criteria: Regular use of tobacco products (including e-cigarettes) other than cigarettes Regular use of nicotine replacement or other tobacco cessation products for purpose of quitting. Pregnant or breastfeeding (due to toxic effects from tobacco products). Planned quit date within the next two months. Does not have a way that the research team can communicate with them by phone or e-mail. Not able to read and write English well enough to complete study activities without translation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dorothy K Hatsukami, PhD
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Minnesota Tobacco Research Program
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55414
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27614097
Citation
Hatsukami DK, Luo X, Dick L, Kangkum M, Allen SS, Murphy SE, Hecht SS, Shields PG, al'Absi M. Reduced nicotine content cigarettes and use of alternative nicotine products: exploratory trial. Addiction. 2017 Jan;112(1):156-167. doi: 10.1111/add.13603. Epub 2016 Nov 2.
Results Reference
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Reduced Nicotine Content Cigarettes and Tobacco Switching Behaviors

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