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New Approaches to Smoking Cessation in Heavy Drinkers

Primary Purpose

Nicotine Dependence, Cigarette Smoking, Alcohol Consumption

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Varenicline
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nicotine Dependence focused on measuring Quit smoking, Quit drinking

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. are at least 18 years of age;
  2. report smoking 100 cigarettes over lifetime and currently smoke at least twice weekly on average in the past 90 days and have a urinary cotinine level of >=30ng/mL by semi-quantitative analysis, and/or >= 2 on a NicAlert dipstick
  3. are interested in quitting smoking;
  4. understand English;
  5. exceed National Institute on Alcohol Abuse and Alcoholism heavy drinking criteria (i.e., for men, >14 drinks/week or 5 drinks/day at least once per month over the past 12 months; for women, >7 drinks/week or >4 drinks/day at least once per month over the past 12 months.

Exclusion Criteria:

  1. meet criteria for alcohol dependence in the past 12 months that is clinically severe defined by

    • a history of seizures, delirium, or hallucinations during alcohol withdrawal;
    • a Clinical Institute Withdrawal Assessment scale (Sullivan et al., 1989) score of > 8;
    • report drinking to avoid withdrawal symptoms, or d) have had prior treatment of withdrawal;
    • have required medical treatment of alcohol withdrawal within the past 6 months;
  2. are currently enrolled in alcohol treatment;
  3. meet criteria for drug dependence in the past 12 months; with the exception of marijuana dependence
  4. exhibit serious psychiatric illness (i.e., schizophrenia, bipolar disorder, severe major depression, panic disorder, borderline personality disorder, organic mood or mental disorders by history or psychological examination;
  5. report current suicidality (past 12 months), or report suicide attempts within the past 10 years, assessed with the Columbia Suicide Severity Rating Scale;
  6. exhibit current, clinically significant physical disease or abnormality based on medical history, physical examination, or routine laboratory evaluation including:

    • any unexplained elevations in liver enzymes (i.e., transaminases, bilirubin);
    • clinically significant, unstable cardiovascular disease/uncontrolled hypertension;
    • hepatic or renal impairment;
    • severe obstructive pulmonary disease;
    • diabetes mellitus requiring insulin or certain oral medications (i.e., sulfonylureas) and an A1C hemoglobin test score of > 7 for participants not prescribed these medications;
    • baseline systolic blood pressure higher than 150 mm Hg or diastolic blood pressure higher than 95 mm Hg;
  7. are cognitively impaired;
  8. are unable to read/understand English;
  9. are a female of childbearing potential who is pregnant, nursing, or not practicing effective contraception (oral, injectable, or implantable contraceptives, intrauterine device, or barrier method with spermicide);
  10. report new onset of psychiatric disorders or new psychotropic medications within the past 3 months, except individuals who are on a stable dose of a Selective Serotonin Reuptake Inhibitor for at least two months or who report occasional use of prescription sleep aids that they are willing to discontinue;
  11. have used another investigational drug within 30 days or have used medications to treat alcohol (e.g., naltrexone, topiramate, acamprosate, disulfiram) or nicotine use (e.g., clonidine, varenicline, bupropion, nicotine replacement) in the past 3 months or intend to use these medications; (prior use of nicotine replacement in situations where smoking is not permitted (e.g., planes) without the intention to quit smoking is not exclusionary at screening)
  12. intend to donate blood or blood products during the treatment phase of the study;
  13. have a history of cancer (except treated basal cell or squamous cell carcinoma of the skin);
  14. have a history of serious hypersensitivity reactions or skin reactions to varenicline.

Sites / Locations

  • Yale University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Integrated Counseling for Tobacco and Alcohol (INT)

Standard Care for Primary Presenting Concern (SC)

Arm Description

Integrated counseling for smoking and alcohol entails weekly counseling for 12-weeks targeting both behaviors. Participants in this condition will also receive 12 weeks of varenicline (Chantix).

Standard care (SC) for primary presenting concern only. For those presenting with the primary concern of tobacco, standard care will involve weekly smoking counseling alone for 12-weeks. For those presenting with the primary concern of alcohol, standard care will involve weekly alcohol counseling alone. Participants in this condition will also receive 12 weeks of varenicline (Chantix).

Outcomes

Primary Outcome Measures

Number of Participants With Smoking Abstinence at 6 Months
Number of participants with point prevalence smoking abstinence (i.e., no smoking, not even a puff over the last 7 days) 6 months after treatment completion.

Secondary Outcome Measures

Log Transformed Percentage of Heavy Drinking Days
Log transformed percentage of heavy drinking days 6 months post treatment start.
Number of Participants Who Completed Treatment.
To assess feasibility/acceptability, the number of participants who completed treatment will be assessed.

Full Information

First Posted
May 27, 2014
Last Updated
February 7, 2020
Sponsor
Yale University
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
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1. Study Identification

Unique Protocol Identification Number
NCT02151591
Brief Title
New Approaches to Smoking Cessation in Heavy Drinkers
Official Title
New Approaches to Smoking Cessation in Heavy Drinkers
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
August 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to develop and test an integrated cognitive-behavioral intervention for smoking and alcohol among heavy drinking smokers. The current pre-pilot phase will be used to refine this protocol for the subsequent randomized, controlled pilot phase. The current study phase has two parts: 1) an intake session and brief physical; 2) a 12-week treatment phase in which participants receive varenicline (Chantix) and weekly, personalized counseling.
Detailed Description
The purpose of the proposed project is to develop and test a 12-week integrated cognitive-behavioral therapy (CBT) intervention for smoking and alcohol (SA) + varenicline (Chantix) among heavy drinking smokers (i.e., CBT for SA). The project involves two phases. In Phase 1, an open-label pre-pilot study of CBT for SA will be conducted with 10 heavy drinking smokers. The primary results of this phase will be used to refine the CBT for SA protocol. In Phase 2, a randomized, controlled pilot study will be conducted with 40 heavy drinking smokers comparing CBT for SA with standard smoking counseling (SC). All participants in the randomized pilot study will also receive varenicline (Chantix). Primary and Study Completion dates were changed 6/2016 to reflect an additional year added year to the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nicotine Dependence, Cigarette Smoking, Alcohol Consumption, Heavy Drinking
Keywords
Quit smoking, Quit drinking

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Integrated Counseling for Tobacco and Alcohol (INT)
Arm Type
Experimental
Arm Description
Integrated counseling for smoking and alcohol entails weekly counseling for 12-weeks targeting both behaviors. Participants in this condition will also receive 12 weeks of varenicline (Chantix).
Arm Title
Standard Care for Primary Presenting Concern (SC)
Arm Type
Other
Arm Description
Standard care (SC) for primary presenting concern only. For those presenting with the primary concern of tobacco, standard care will involve weekly smoking counseling alone for 12-weeks. For those presenting with the primary concern of alcohol, standard care will involve weekly alcohol counseling alone. Participants in this condition will also receive 12 weeks of varenicline (Chantix).
Intervention Type
Drug
Intervention Name(s)
Varenicline
Other Intervention Name(s)
Chantix
Intervention Description
12-weeks of treatment. Dose will be titrated as follows: Days 1-3: 1 0.5mg tablet once per day Days 4-7: 1 0.5mg tablet twice per day Day 8 - Week 11: 1 1mg tablet twice per day
Primary Outcome Measure Information:
Title
Number of Participants With Smoking Abstinence at 6 Months
Description
Number of participants with point prevalence smoking abstinence (i.e., no smoking, not even a puff over the last 7 days) 6 months after treatment completion.
Time Frame
6 months post treatment start
Secondary Outcome Measure Information:
Title
Log Transformed Percentage of Heavy Drinking Days
Description
Log transformed percentage of heavy drinking days 6 months post treatment start.
Time Frame
6 months post treatment start
Title
Number of Participants Who Completed Treatment.
Description
To assess feasibility/acceptability, the number of participants who completed treatment will be assessed.
Time Frame
12 weeks

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
based on self-reported gender
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: are at least 18 years of age; report smoking 100 cigarettes over lifetime and currently smoke at least twice weekly on average in the past 90 days and have a urinary cotinine level of >=30ng/mL by semi-quantitative analysis, and/or >= 2 on a NicAlert dipstick are interested in quitting smoking; understand English; exceed National Institute on Alcohol Abuse and Alcoholism heavy drinking criteria (i.e., for men, >14 drinks/week or 5 drinks/day at least once per month over the past 12 months; for women, >7 drinks/week or >4 drinks/day at least once per month over the past 12 months. Exclusion Criteria: meet criteria for alcohol dependence in the past 12 months that is clinically severe defined by a history of seizures, delirium, or hallucinations during alcohol withdrawal; a Clinical Institute Withdrawal Assessment scale (Sullivan et al., 1989) score of > 8; report drinking to avoid withdrawal symptoms, or d) have had prior treatment of withdrawal; have required medical treatment of alcohol withdrawal within the past 6 months; are currently enrolled in alcohol treatment; meet criteria for drug dependence in the past 12 months; with the exception of marijuana dependence exhibit serious psychiatric illness (i.e., schizophrenia, bipolar disorder, severe major depression, panic disorder, borderline personality disorder, organic mood or mental disorders by history or psychological examination; report current suicidality (past 12 months), or report suicide attempts within the past 10 years, assessed with the Columbia Suicide Severity Rating Scale; exhibit current, clinically significant physical disease or abnormality based on medical history, physical examination, or routine laboratory evaluation including: any unexplained elevations in liver enzymes (i.e., transaminases, bilirubin); clinically significant, unstable cardiovascular disease/uncontrolled hypertension; hepatic or renal impairment; severe obstructive pulmonary disease; diabetes mellitus requiring insulin or certain oral medications (i.e., sulfonylureas) and an A1C hemoglobin test score of > 7 for participants not prescribed these medications; baseline systolic blood pressure higher than 150 mm Hg or diastolic blood pressure higher than 95 mm Hg; are cognitively impaired; are unable to read/understand English; are a female of childbearing potential who is pregnant, nursing, or not practicing effective contraception (oral, injectable, or implantable contraceptives, intrauterine device, or barrier method with spermicide); report new onset of psychiatric disorders or new psychotropic medications within the past 3 months, except individuals who are on a stable dose of a Selective Serotonin Reuptake Inhibitor for at least two months or who report occasional use of prescription sleep aids that they are willing to discontinue; have used another investigational drug within 30 days or have used medications to treat alcohol (e.g., naltrexone, topiramate, acamprosate, disulfiram) or nicotine use (e.g., clonidine, varenicline, bupropion, nicotine replacement) in the past 3 months or intend to use these medications; (prior use of nicotine replacement in situations where smoking is not permitted (e.g., planes) without the intention to quit smoking is not exclusionary at screening) intend to donate blood or blood products during the treatment phase of the study; have a history of cancer (except treated basal cell or squamous cell carcinoma of the skin); have a history of serious hypersensitivity reactions or skin reactions to varenicline.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa Fucito, PhD
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale University School of Medicine
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06511
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
A de-identified dataset will be made available to researchers who request data from the PI
IPD Sharing Time Frame
The data will be available upon final publication of the primary paper.
IPD Sharing Access Criteria
Upon request to PI

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New Approaches to Smoking Cessation in Heavy Drinkers

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