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Project 3, Study 2: Extended Exposure to Low Nicotine Content Cigarettes in People With Current Affective Disorders

Primary Purpose

Tobacco Use Disorder

Status

Completed

Phase

Phase 1

Locations

United States

Study Type

Interventional

Intervention

Very low nicotine content cigarettes

About this trial

This is an interventional basic science trial for Tobacco Use Disorder focused on measuring Biomarkers of exposure, Compensatory smoking, Nicotine dependence, Reduced nicotine cigarettes, Tobacco withdrawal, Women, Health disparities, Vulnerable populations

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Male or Female
Ages 18-70
Past-year major depressive disorder, dysthymic disorder, generalized anxiety disorder, post-traumatic stress disorder, obsessive-compulsive disorder, phobia, or panic disorder with or without agoraphobia, based on MINI structured interview, OR lifetime diagnosis of one of the above based on MINI with a self-report of currently receiving treatment (prescribed psychoactive medication, behavioral therapy, etc.)
Report smoking 5 or more cigarettes per day for the past year
Provide an intake breath CO sample > 8 ppm
Be without current substance abuse/dependence other than nicotine
Be sufficiently literate to complete the research-related tasks
Be in good physical health without serious illness or change in health in the past 3 months as determined by the licensed medical professional at each site
Not pregnant or nursing and report using oral, implant, patch, ring, IUD, injection or barrier contraceptives or report being surgically sterile or post-menopausal
Report no significant use of other tobacco or nicotine products within the past month (> 9 days in the past 30)

Exclusion Criteria:

Any prior regular use (used as primary cigarette outside of the laboratory) of Spectrum cigarettes (i.e., research cigarettes with reduced nicotine content)
Exclusive use of roll-your-own cigarettes
Planning to quit smoking in the next 30 days
A quit attempt in the past 30 days resulting in > 3 days of abstinence
Positive toxicology screen for illicit drugs not including marijuana (participants with valid prescriptions will not be excluded and participants with a positive toxicology screen will be allowed to re-screen once)
Breath alcohol level > 0.01 (participants with a positive screen will be allowed to re-screen once)
Self-report of binge drinking alcohol (> 9 days in the past 30, 4/5 drinks in 2 hours for women/men
Systolic blood pressure below 90 mmHg or greater than or equal to 160 mmHg (participants outside the range will be allowed to re-screen once)
Diastolic blood pressure below 50 mmHg or greater than or equal to 100 mmHg (participants outside the range will be allowed to re-screen once)
Breath CO > 80 ppm
Heart rate below 45 or greater than or equal to 115 bpm (participants outside the range will be allowed to re-screen once)
Currently seeking treatment for smoking cessation
Have used nicotine replacement, bupropion or other pharmacotherapies as cessation aids in the past month (bupropion for treatment of depression will be allowed)
Unstable psychiatric conditions (psychiatric medication changes in the past 4 weeks)
Current symptoms of psychosis, dementia or mania
Suicidal ideation in past month
Suicide attempt in past 6 months
Participation in another research study in the past 30 days

Sites / Locations

Brown University
University of Vermont

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Arm Label

0.8 mg nicotine

0.12 mg nicotine

0.03 mg nicotine

Arm Description

0.8 mg nicotine cigarettes

0.12 mg nicotine cigarettes

0.03 mg nicotine cigarettes

Outcomes

Primary Outcome Measures

Cigarettes Per Day (CPD)

Participant reported number of cigarettes smoked per day at Week 12

Secondary Outcome Measures

Full Information

NCT ID

NCT02232737

First Posted

September 3, 2014

Last Updated

November 15, 2022

Sponsor

Brown University

Collaborators

University of Vermont, National Institute on Drug Abuse (NIDA)

1. Study Identification

Unique Protocol Identification Number

NCT02232737

Brief Title

Project 3, Study 2: Extended Exposure to Low Nicotine Content Cigarettes in People With Current Affective Disorders

Official Title

Project 3, Study 2: Extended Exposure to Low Nicotine Content Cigarettes in People With Current Affective Disorders

Study Type

Interventional

2. Study Status

Record Verification Date

October 2022

Overall Recruitment Status

Completed

Study Start Date

October 7, 2016 (Actual)

Primary Completion Date

January 14, 2019 (Actual)

Study Completion Date

January 14, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

Brown University

Collaborators

University of Vermont, National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

This study will examine extended exposure to cigarettes varying in nicotine content among disadvantaged women. Adults with affective disorders are at increased risk for smoking, nicotine dependence, and using high nicotine yield cigarettes and are also at significantly increased risk for smoking-related adverse health consequences, including site-specific cancers, heart disease, and premature death. Studies testing an innovative regulatory strategy of reducing the nicotine content of cigarettes to a non-addictive level have shown promising beneficial effects (decreased smoking rate, reduced toxicant exposure, and increased cessation) in the general population of smokers. However, these studies have uniformly excluded vulnerable populations like those with affective disorders who may respond differently considering their greater vulnerability to smoking and nicotine dependence. Thus, little is known scientifically about how this highly vulnerable subgroup of smokers might respond to a nicotine reduction policy. This project is designed to address that substantial knowledge gap. This same study was also conducted in two additional vulnerable populations under a similar protocol.

Detailed Description

The primary overall objective of these studies is to evaluate the effects of extended exposure to cigarettes differing in nicotine content in adult men and women with affective disorders using a 3-condition, parallel groups design. After a baseline period in which daily smoking rate and other baseline assessments are completed, participants will be randomly assigned to one of three cigarette conditions (nicotine content: 0.03, 0.12, and 0.8 mg nicotine of tobacco) for the 12-week experimental period. The cigarettes to be used in this study were made under an NIH contract with production being overseen by the Research Triangle Institute (referred to as "Spectrum cigarettes"). NIH currently has approximately 10 million of these cigarettes (of varying types) for research purposes. The cigarettes selected for the study span the range of yields likely to produce the hypothesized effects, as described above. The Spectrum cigarettes are not currently commercially available, although they are similar in many ways to marketed cigarettes (e.g., similar manufacturing, filter, paper, etc.). The primary overall objective of this study is to evaluate the effects of extended exposure to cigarettes differing in nicotine content in adult men and women with affective disorders using a 3-condition, parallel groups design. After a baseline period in which daily smoking rate and other baseline assessments are completed, participants will be randomly assigned to one of three cigarette conditions (nicotine content: 0.03 mg, 0.12 mg, and 0.8 mg nicotine of tobacco) for the 12-week experimental period. Participants will be seen weekly throughout the 12-week experimental period to obtain research cigarettes. Cigarettes smoked per day will be obtained by participants completing daily Interactive Voice Response (IVR) reports of cigarettes in past 24 hours. This daily data will be used to calculate weekly means, with week-12 means serving as the primary outcome. This same study was conducted in two additional vulnerable populations under a similar protocol, with differences between protocols consisting of data collection specific to that vulnerable population. This included information such as use and timing of opioid maintenance therapy for individuals with opioid-use disorder and other measures relevant to disadvantaged women of reproductive age. In order to explore potential differences across individuals with different vulnerabilities, data from all three studies were combined for analysis. A vulnerable population-by-condition or population-by-condition-by-time interaction term was included in all analyses. In the event that these interaction terms were statistically significant, all pairwise comparisons were conducted using a Bonferroni multiple comparison adjustment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Tobacco Use Disorder

Keywords

Biomarkers of exposure, Compensatory smoking, Nicotine dependence, Reduced nicotine cigarettes, Tobacco withdrawal, Women, Health disparities, Vulnerable populations

7. Study Design

Primary Purpose

Basic Science

Study Phase

Phase 1, Phase 2

Interventional Study Model

Parallel Assignment

Model Description

This study was one of three multi-site clinical trials conducted in three different vulnerable populations under a similar protocol, with differences between protocols consisting of data collection specific to that vulnerable population. This included information such as use and timing of opioid maintenance therapy for individuals with opioid-use disorder or additional assessments related to disadvantaged women of reproductive age. In order to explore potential differences across individuals with different vulnerabilities, data from all three studies were combined for analysis. A vulnerable population-by-condition or population-by- condition-by-time interaction term was included in all analyses. In the event that these interaction terms were statistically significant, all pairwise comparisons were conducted using a Bonferroni multiple comparison adjustment. Please see Statistical Analysis Plan for more details.

Masking

ParticipantInvestigator

Allocation

Randomized

Enrollment

775 (Actual)

8. Arms, Groups, and Interventions

Arm Title

0.8 mg nicotine

Arm Type

Experimental

Arm Description

0.8 mg nicotine cigarettes

Arm Title

0.12 mg nicotine

Arm Type

Experimental

Arm Description

0.12 mg nicotine cigarettes

Arm Title

0.03 mg nicotine

Arm Type

Experimental

Arm Description

0.03 mg nicotine cigarettes

Intervention Type

Other

Intervention Name(s)

Very low nicotine content cigarettes

Primary Outcome Measure Information:

Title

Cigarettes Per Day (CPD)

Description

Participant reported number of cigarettes smoked per day at Week 12

Time Frame

12 weeks

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Maximum Age & Unit of Time

70 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Male or Female Ages 18-70 Past-year major depressive disorder, dysthymic disorder, generalized anxiety disorder, post-traumatic stress disorder, obsessive-compulsive disorder, phobia, or panic disorder with or without agoraphobia, based on Mini-Neuropsychiatric Interview (MINI) structured interview, OR lifetime diagnosis of one of the above based on MINI with a self-report of currently receiving treatment (prescribed psychoactive medication, behavioral therapy, etc.) Report smoking 5 or more cigarettes per day for the past year Provide an intake breath Carbon Monoxide (CO) sample > 8 ppm Be without current substance abuse/dependence other than nicotine Be sufficiently literate to complete the research-related tasks Be in good physical health without serious illness or change in health in the past 3 months as determined by the licensed medical professional at each site Not pregnant or nursing and report using oral, implant, patch, ring, intrauterine device (IUD), injection or barrier contraceptives or report being surgically sterile or post-menopausal Report no significant use of other tobacco or nicotine products within the past month (> 9 days in the past 30) Exclusion Criteria: Any prior regular use (used as primary cigarette outside of the laboratory) of Spectrum cigarettes (i.e., research cigarettes with reduced nicotine content) Exclusive use of roll-your-own cigarettes Planning to quit smoking in the next 30 days A quit attempt in the past 30 days resulting in > 3 days of abstinence Positive toxicology screen for illicit drugs not including marijuana (participants with valid prescriptions will not be excluded and participants with a positive toxicology screen will be allowed to re-screen once) Breath alcohol level > 0.01 (participants with a positive screen will be allowed to re-screen once) Self-report of binge drinking alcohol (> 9 days in the past 30, 4/5 drinks in 2 hours for women/men Systolic blood pressure below 90 mmHg or greater than or equal to 160 mmHg (participants outside the range will be allowed to re-screen once) Diastolic blood pressure below 50 mmHg or greater than or equal to 100 mmHg (participants outside the range will be allowed to re-screen once) Breath CO > 80 ppm Heart rate below 45 or greater than or equal to 115 bpm (participants outside the range will be allowed to re-screen once) Currently seeking treatment for smoking cessation Have used nicotine replacement, bupropion or other pharmacotherapies as cessation aids in the past month (bupropion for treatment of depression will be allowed) Unstable psychiatric conditions (psychiatric medication changes in the past 4 weeks) Current symptoms of psychosis, dementia or mania Suicidal ideation in past month Suicide attempt in past 6 months Participation in another research study in the past 30 days

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Stephen T Higgins, PhD

Organizational Affiliation

University of Vermont

Official's Role

Study Director

Facility Information:

Facility Name

Brown University

City

Providence

State/Province

Rhode Island

ZIP/Postal Code

02912

Country

United States

Facility Name

University of Vermont

City

Burlington

State/Province

Vermont

ZIP/Postal Code

05401

Country

United States

12. IPD Sharing Statement

Citations:

PubMed Identifier

36208817

Citation

Gaalema DE, Snell LM, Tidey JW, Sigmon SC, Heil SH, Lee DC, Bunn JY, Park C, Hughes JR, Higgins ST. Potential effects of nicotine content in cigarettes on use of other substances. Prev Med. 2022 Dec;165(Pt B):107290. doi: 10.1016/j.ypmed.2022.107290. Epub 2022 Oct 5.

Results Reference

derived

PubMed Identifier

34255068

Citation

Oliver AC, DeSarno M, Irvin CG, Kaminsky D, Tidey JW, Sigmon SC, Heil SH, Gaalema DE, Lee D, Bunn JY, Davis DR, Streck JM, Gallagher T, Higgins ST. Effects of Reduced Nicotine Content Cigarettes on Fractional Exhaled Nitric Oxide and Self-Reported Respiratory Health Outcomes Among Smokers With Psychiatric Conditions or Socioeconomic Disadvantage. Nicotine Tob Res. 2022 Jan 1;24(1):135-140. doi: 10.1093/ntr/ntab145.

Results Reference

derived

PubMed Identifier

34242666

Citation

Higgins ST, DeSarno M, Bunn JY, Gaalema DE, Leventhal AM, Davis DR, Streck JM, Harfmann RF, Markesich C, Orr E, Sigmon SC, Heil SH, Tidey JW, Lee D, Hughes JR. Cumulative vulnerabilities as a potential moderator of response to reduced nicotine content cigarettes. Prev Med. 2021 Nov;152(Pt 2):106714. doi: 10.1016/j.ypmed.2021.106714. Epub 2021 Jul 7.

Results Reference

derived

PubMed Identifier

33079196

Citation

Higgins ST, Tidey JW, Sigmon SC, Heil SH, Gaalema DE, Lee D, Hughes JR, Villanti AC, Bunn JY, Davis DR, Bergeria CL, Streck JM, Parker MA, Miller ME, DeSarno M, Priest JS, Cioe P, MacLeod D, Barrows A, Markesich C, Harfmann RF. Changes in Cigarette Consumption With Reduced Nicotine Content Cigarettes Among Smokers With Psychiatric Conditions or Socioeconomic Disadvantage: 3 Randomized Clinical Trials. JAMA Netw Open. 2020 Oct 1;3(10):e2019311. doi: 10.1001/jamanetworkopen.2020.19311.

Results Reference

derived

PubMed Identifier

32628945

Citation

Higgins ST, DeSarno M, Davis DR, Nighbor T, Streck JM, Adise S, Harfmann R, Nesheim-Case R, Markesich C, Reed D, Tyndale RF, Gaalema DE, Heil SH, Sigmon SC, Tidey JW, Villanti AC, Lee D, Hughes JR, Bunn JY. Relating individual differences in nicotine dependence severity to underpinning motivational and pharmacological processes among smokers from vulnerable populations. Prev Med. 2020 Nov;140:106189. doi: 10.1016/j.ypmed.2020.106189. Epub 2020 Jul 3.

Results Reference

derived

Learn more about this trial

Project 3, Study 2: Extended Exposure to Low Nicotine Content Cigarettes in People With Current Affective Disorders

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