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Smoking Cessation Treatment for Methadone Maintenance Patients

Primary Purpose

Smoking Cessation, Substance-Related Disorders

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Varenicline
Placebo
Sponsored by
Albert Einstein College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Smoking Cessation focused on measuring methadone maintenance

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 or older
  • English speaking
  • Smoked at least 100 cigarettes/lifetime
  • Smokes 5 or more cigarettes per day
  • Interested in quitting smoking (preparation or contemplation state of change)
  • Enrolled in Einstein/Montefiore methadone program for 3 or more months
  • Stable methadone dose for 2 weeks
  • Agree to use contraception throughout the trial (among women with reproductive potential)
  • Willing to participate in all study components
  • Able to provide informed consent

Exclusion Criteria:

  • Serious or unstable HIV/AIDS, liver, cardiovascular, or pulmonary disease
  • Psychiatric instability
  • Women who are pregnant, breastfeeding, or contemplating pregnancy
  • Creatinine clearance less than 30 mL/min

Sites / Locations

  • Albert Einstein College of Medicine of Yeshiva University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Varenicline

Placebo

Arm Description

Drug treatment in combination with telephone quitline referral and brief individual counseling based on PHS guidelines at weeks 2, 4, 8, and 12

Matched placebo capsules in combination with telephone quitline referral and brief individual counseling based on PHS guidelines at weeks 2, 4, 8, and 12

Outcomes

Primary Outcome Measures

Biochemically Verified Abstinence Verified With Expired Carbon Monoxide (CO) < 8 p.p.m.

Secondary Outcome Measures

Biochemically Verified Abstinence Verified With Expired Carbon Monoxide (CO) < 8 p.p.m.
Number of Counseling Visits Completed
Participants were offered 5 counseling visits at weeks 0, 2, 4, 8, 12.
Number of Study Visits Completed
Mean number of study visit completed out of a possible total of 6 study visits at weeks 0, 2, 4, 8, 12 and 24.
7-day Point Prevalence Abstinence at 12 Weeks as Verified by Salivary Cotinine.
Threshold of salivary cotinine ≤ 15 ng/ml was prespecified. Salivary cotinine was measured among participants who self-reported 7-day point prevalence abstinence using a semi-quantitative assay (Nymox NicAlert™).
Number of Cigarettes Smoked Per Day
Number of Participants With an Attempt to Quit Smoking That Lasted ≥ 24 Hours
Confidence in Quitting Smoking (1-10 Scale)
Confidence of quitting smoking measure on a scale of 1-10 (10= high levels of quit confidence).
Importance of Quitting Smoking (1-10 Scale)
Importance of quitting smoking measured on a scale of 1-10 (10=high levels of quit importance).
Adverse Medication Effects
Number of Participants With Severe Global Psychiatric Symptoms Assessed by the Brief Symptom Inventory
Number of Patients With Suicial Ideation (Wishes to be Dead, or Thoughts of Killing Self) Assessed Using the Columbia Suicide Severity Scale
Number of Participants With Major Depressive Episode, Assessed by the Mini-International Neuropsychiatric Interview
Number of Participants With Manic Episode, Assessed by the Mini-International Neuropsychiatric Interview
Number of Participants With Psychotic Disorder, Assessed by the Mini-International Neuropsychiatric Interview

Full Information

First Posted
December 7, 2009
Last Updated
May 4, 2021
Sponsor
Albert Einstein College of Medicine
Collaborators
National Center for Research Resources (NCRR)
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1. Study Identification

Unique Protocol Identification Number
NCT01027754
Brief Title
Smoking Cessation Treatment for Methadone Maintenance Patients
Official Title
Smoking Cessation Treatment for Methadone Maintenance Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Albert Einstein College of Medicine
Collaborators
National Center for Research Resources (NCRR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients in substance abuse treatment smoke four times more than non-substance abusers, and suffer high rates of tobacco-related disease and death. While many quit smoking treatments exist that have been shown to help non-substance abusers quit smoking, little is known about what treatments work for patients in substance abuse treatment. The drug varenicline (Chantix) has been shown to be more effective at helping people quit smoking than nicotine replacement therapy, bupropion or placebo. However, varenicline has not yet been studied in patients in substance abuse treatment. The study aims to evaluate the feasibility, effectiveness and safety of varenicline, in combination with counseling, in methadone maintained smokers. It also aims to evaluate the link between quitting smoking and alcohol and illicit drug use in methadone maintained smokers. We hypothesize that participants receiving varenicline will have higher abstinence from smoking than participants receiving placebo and that participants taking varenicline will not have significantly more adverse reactions than were described in the general population in other studies. We also hypothesize that compared to continued smokers, tobacco abstainers will be more likely to be abstinent from alcohol or illicit drugs.
Detailed Description
Patients in substance abuse treatment smoke four times more than non-substance abusers, and suffer high rates of tobacco-related disease and death. While many quit smoking treatments exist that have been shown to help non-substance abusers quit smoking, little is known about what treatments work for patients in substance abuse treatment. The drug varenicline (Chantix) has been shown to be more effective at helping people quit smoking than nicotine replacement therapy, bupropion or placebo. However, varenicline has not yet been studied in patients in substance abuse treatment. The study aims to evaluate the feasibility, effectiveness and safety of varenicline, in combination with counseling, in methadone maintained smokers. It also aims to evaluate the link between quitting smoking and alcohol and illicit drug use in methadone maintained smokers. We hypothesize that participants receiving varenicline will have higher abstinence from smoking than participants receiving placebo and that participants taking varenicline will not have significantly more adverse reactions than were described in the general population in other studies. We also hypothesize that compared to continued smokers, tobacco abstainers will be more likely to be abstinent from alcohol or illicit drugs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Smoking Cessation, Substance-Related Disorders
Keywords
methadone maintenance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Varenicline
Arm Type
Experimental
Arm Description
Drug treatment in combination with telephone quitline referral and brief individual counseling based on PHS guidelines at weeks 2, 4, 8, and 12
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matched placebo capsules in combination with telephone quitline referral and brief individual counseling based on PHS guidelines at weeks 2, 4, 8, and 12
Intervention Type
Drug
Intervention Name(s)
Varenicline
Other Intervention Name(s)
Chantix
Intervention Description
Days 1-3: 0.5 mg once a day Days 4-7: 0.5 mg twice a day Days 8-84: 1 mg twice a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Matched capsules
Intervention Description
Days 1-3: 1 pill daily Days 4-7: 2 pills daily Days 8-84: 2 pills daily
Primary Outcome Measure Information:
Title
Biochemically Verified Abstinence Verified With Expired Carbon Monoxide (CO) < 8 p.p.m.
Time Frame
Week 12
Secondary Outcome Measure Information:
Title
Biochemically Verified Abstinence Verified With Expired Carbon Monoxide (CO) < 8 p.p.m.
Time Frame
Week 24
Title
Number of Counseling Visits Completed
Description
Participants were offered 5 counseling visits at weeks 0, 2, 4, 8, 12.
Time Frame
End of 12 week intervention period
Title
Number of Study Visits Completed
Description
Mean number of study visit completed out of a possible total of 6 study visits at weeks 0, 2, 4, 8, 12 and 24.
Time Frame
24 weeks
Title
7-day Point Prevalence Abstinence at 12 Weeks as Verified by Salivary Cotinine.
Description
Threshold of salivary cotinine ≤ 15 ng/ml was prespecified. Salivary cotinine was measured among participants who self-reported 7-day point prevalence abstinence using a semi-quantitative assay (Nymox NicAlert™).
Time Frame
Weeks 2, 4, 8, 12, and 24
Title
Number of Cigarettes Smoked Per Day
Time Frame
Weeks 2, 4, 8, 12, and 24
Title
Number of Participants With an Attempt to Quit Smoking That Lasted ≥ 24 Hours
Time Frame
Weeks 2, 4, 8, 12, and 24
Title
Confidence in Quitting Smoking (1-10 Scale)
Description
Confidence of quitting smoking measure on a scale of 1-10 (10= high levels of quit confidence).
Time Frame
Weeks 2, 4, 8, 12, and 24
Title
Importance of Quitting Smoking (1-10 Scale)
Description
Importance of quitting smoking measured on a scale of 1-10 (10=high levels of quit importance).
Time Frame
Weeks 2, 4, 8, 12, and 24
Title
Adverse Medication Effects
Time Frame
over the intervention period (measured at weeks 2, 4, 8, 12, and 24)
Title
Number of Participants With Severe Global Psychiatric Symptoms Assessed by the Brief Symptom Inventory
Time Frame
over the intervention period (measured at weeks 2, 4, 8, 12, and 24)
Title
Number of Patients With Suicial Ideation (Wishes to be Dead, or Thoughts of Killing Self) Assessed Using the Columbia Suicide Severity Scale
Time Frame
over the intervention period (measured at weeks 2, 4, 8, 12, and 24)
Title
Number of Participants With Major Depressive Episode, Assessed by the Mini-International Neuropsychiatric Interview
Time Frame
over the intervention period (measured at weeks 2, 4, 8, 12, and 24)
Title
Number of Participants With Manic Episode, Assessed by the Mini-International Neuropsychiatric Interview
Time Frame
over the intervention period (measured at weeks 2, 4, 8, 12, and 24)
Title
Number of Participants With Psychotic Disorder, Assessed by the Mini-International Neuropsychiatric Interview
Time Frame
over the intervention period (measured at weeks 2, 4, 8, 12, and 24)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or older English speaking Smoked at least 100 cigarettes/lifetime Smokes 5 or more cigarettes per day Interested in quitting smoking (preparation or contemplation state of change) Enrolled in Einstein/Montefiore methadone program for 3 or more months Stable methadone dose for 2 weeks Agree to use contraception throughout the trial (among women with reproductive potential) Willing to participate in all study components Able to provide informed consent Exclusion Criteria: Serious or unstable HIV/AIDS, liver, cardiovascular, or pulmonary disease Psychiatric instability Women who are pregnant, breastfeeding, or contemplating pregnancy Creatinine clearance less than 30 mL/min
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shadi Nahvi, M.D., M.S.
Organizational Affiliation
Albert Einstein College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Albert Einstein College of Medicine of Yeshiva University
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24862167
Citation
Nahvi S, Ning Y, Segal KS, Richter KP, Arnsten JH. Varenicline efficacy and safety among methadone maintained smokers: a randomized placebo-controlled trial. Addiction. 2014 Sep;109(9):1554-63. doi: 10.1111/add.12631. Epub 2014 Jun 27.
Results Reference
derived

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Smoking Cessation Treatment for Methadone Maintenance Patients

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