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Developing a Smoking Cessation Intervention for Methadone Maintained Smokers

Primary Purpose

Nicotine Dependence, Opiate Dependence

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Intensive, tailored intervention
NJ Quitline Referral
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nicotine Dependence focused on measuring smoking cessation, methadone treatment, nicotine addiction, drug treatment, drug addiction, tobacco dependence

Eligibility Criteria

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

Inclusion Criteria:

  • Enrolled in methadone treatment for at least three months
  • Able to give informed consent
  • Willing and able to participate in all study activities
  • Smoked at least 100 cigarettes during their lifetime
  • Currently smoke every day or most days
  • Has access to a working telephone
  • Interested in participating in a smoking cessation intervention and quitting smoking within the next six months

Exclusion Criteria:

  • Unable to speak English fluently
  • Took smoking cessation related medication or participated in smoking cessation counseling in the past three months
  • Pregnant or breastfeeding or planning on becoming pregnant or breastfeeding during the next six months

Sites / Locations

  • Rutgers Robert Wood Johnson Medical School

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intensive, tailored intervention

Control Intervention

Arm Description

Participants in the intensive intervention condition will receive eight individual counseling sessions, with a smoking cessation counselor, over three months. Each session will last approximately 45 minutes and occur in the methadone clinic. Participant treatment needs will be assessed during the first session and the intervention will be tailored to the participants' needs. Prior to quitting participants will receive nicotine replacement patches and lozenges and instructions on how to use them.

Participants randomized to the control intervention will receive a referral to the NJ Quitline (a telephone smoking cessation counseling service). Participants will receive a brochure and information about the referral. Study staff will contact the NJ Quitline for control participants, and a counselor from the Quitline will call control participants.

Outcomes

Primary Outcome Measures

Number of Participants Who Experienced Seven-day Point Prevalence Smoking Abstinence
Self-reported not smoking "even a puff" within the previous seven days, and exhaled carbon monoxide reading of <8 parts per million.

Secondary Outcome Measures

Median Number of Cigarettes Participants Smoked Per Day During the Past Week
Self-reported, median number of cigarettes per day during the previous seven days
Number of Participants Who Experienced Any Quit Attempts Since Baseline
Self-reported, smoke free for 24 hours or more since baseline (yes/no)
Number of Participants Who Experienced Seven-day Point Prevalence of Smoking Abstinence
Self-reported not smoking "even a puff" within the previous seven days, and exhaled carbon monoxide reading of <8 parts per million.
Median Number of Cigarettes Smoked Per Day During the Past Week
Self-reported, median number of cigarettes per day during the previous seven days
Number of Participants Who Experienced Any Quit Attempts Since Enrollment
Self-reported, smoke free for 24 hours or more since baseline (yes/no)

Full Information

First Posted
June 27, 2011
Last Updated
September 4, 2018
Sponsor
Rutgers, The State University of New Jersey
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01393392
Brief Title
Developing a Smoking Cessation Intervention for Methadone Maintained Smokers
Official Title
Developing a Smoking Cessation Intervention for Methadone Maintained Smokers
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to pilot and evaluate, in a randomized controlled trial, the immediate and long-term effects of a newly developed, tailored, intensive smoking cessation intervention among methadone maintained smokers and compared to a control condition (facilitated referral to the NJ Quitline). The newly developed intervention is evidence based, addresses the unique needs of methadone maintained smokers, is intensive, can be tailored to the individual, and builds on the strengths as well as addresses the gaps in previous treatments for methadone maintained smokers. The investigators hypothesize that: (1) three months and six months after beginning treatment, those in the tailored intervention condition will be more likely to be abstinent from smoking than those in the control intervention condition (primary outcome); (2) there will be a greater relapse rate in the control intervention condition between the three and six month follow-up points than in the tailored intervention condition; (3) three and six months after beginning treatment, those in the tailored intervention condition will have better secondary smoking related outcomes (smoked fewer cigarettes per day in the past week, be more ready to quit, have greater self-efficacy for quitting, experience less nicotine dependence, and be more likely to have made a quit attempt) than those in the control intervention condition; (4) three and six months after beginning treatment, those in the tailored intervention condition will have better utilization of and adherence to smoking cessation pharmacotherapy, better mental and physical health, less perceived stress, greater social support, less drug and alcohol use, and greater involvement in drug and alcohol treatment than those in the control intervention condition; and (5) the newly created tailored intervention will be feasible and acceptable. .
Detailed Description
Most individuals in methadone maintenance treatment are tobacco smokers. Also, people in methadone treatment are more likely to experience the health issues related to smoking than the general population. Yet, research has found that smokers receiving methadone treatment are interested in quitting and receiving tobacco cessation treatment, and people in drug treatment who quit smoking are less likely to use drugs. To better help methadone maintained smokers quit smoking and prevent them from starting smoking again, we want to evaluate the effects of a new smoking cessation counseling intervention, designed for methadone maintained smokers as compared to a smoking cessation counseling intervention used with the general population. Eligible participants will: Be English speaking (i.e., able to participate in counseling sessions in English and to complete study interviews in English); Be enrolled in methadone treatment for at least three months; Be able to give informed consent; Be willing and able to participate in all study activities; Not have taken smoking cessation related medication or participated in smoking cessation counseling in the past six months; Have smoked at least 100 cigarettes during their lifetime and currently smoke every day or most days; Not currently be pregnant or breastfeeding or plan on getting pregnant or breastfeeding during the next six months; Have access to a working telephone; and, Be interested in participating in a smoking cessation intervention and quitting smoking within the next six months. Participants will be randomly assigned to receive either a smoking cessation intervention tailored for methadone maintained smokers or a referral to a smoking cessation program available to the general population (NJ Quitline). Participants assigned to receive the tailored intervention, will participate in approximately eight individual counseling sessions, with a smoking cessation counselor, over three months. Each session will last approximately 45 minutes and occur in the participant's methadone clinic. Treatment needs will be assessed during the first session and the intervention will be tailored to participants' needs. Prior to quitting participants will receive nicotine replacement patches and lozenges and instructions on how to use them. Study staff will contact the NJ Quitline for participants assigned to the control condition, and a counselor from the Quitline will call them. Regardless of treatment assignment, participants will be asked to provide a urine sample for a drug test and pregnancy test (for women) and complete an interview, using a computer or face-to-face, before beginning treatment or receiving the NJ Quitline referral and three months and six months after study enrollment.Each interview will take approximately 45 minutes to one hour to complete. Participants will receive a $20 gift card for completing each research visit (i.e., computer or face-to-face interview), but will not be reimbursed for counseling visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nicotine Dependence, Opiate Dependence
Keywords
smoking cessation, methadone treatment, nicotine addiction, drug treatment, drug addiction, tobacco dependence

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Intensive, tailored intervention
Arm Type
Experimental
Arm Description
Participants in the intensive intervention condition will receive eight individual counseling sessions, with a smoking cessation counselor, over three months. Each session will last approximately 45 minutes and occur in the methadone clinic. Participant treatment needs will be assessed during the first session and the intervention will be tailored to the participants' needs. Prior to quitting participants will receive nicotine replacement patches and lozenges and instructions on how to use them.
Arm Title
Control Intervention
Arm Type
Active Comparator
Arm Description
Participants randomized to the control intervention will receive a referral to the NJ Quitline (a telephone smoking cessation counseling service). Participants will receive a brochure and information about the referral. Study staff will contact the NJ Quitline for control participants, and a counselor from the Quitline will call control participants.
Intervention Type
Behavioral
Intervention Name(s)
Intensive, tailored intervention
Other Intervention Name(s)
Smokers in Methadone Treatment Intervention, IMB Model Based Smoking Cessation Intervention
Intervention Description
Eight, 45 minute counseling sessions, tailored to the individual and based on the Information-Motivation-Behavioral Skills model of behavior change. Incorporates motivational interviewing, education, cognitive-behavioral skills training. 12 week course of nicotine replacement patches provided. Nicotine lozenges also provided.
Intervention Type
Behavioral
Intervention Name(s)
NJ Quitline Referral
Other Intervention Name(s)
Standard of Care Smoking Cessation Intervention, General Population Smoking Cessation Intervention
Intervention Description
Participants will receive a facilitated referral to the NJ Quitline (i.e. fax to quit).
Primary Outcome Measure Information:
Title
Number of Participants Who Experienced Seven-day Point Prevalence Smoking Abstinence
Description
Self-reported not smoking "even a puff" within the previous seven days, and exhaled carbon monoxide reading of <8 parts per million.
Time Frame
during the previous seven days at three months post baseline
Secondary Outcome Measure Information:
Title
Median Number of Cigarettes Participants Smoked Per Day During the Past Week
Description
Self-reported, median number of cigarettes per day during the previous seven days
Time Frame
during the previous seven days at three months post baseline
Title
Number of Participants Who Experienced Any Quit Attempts Since Baseline
Description
Self-reported, smoke free for 24 hours or more since baseline (yes/no)
Time Frame
During the period between baseline and three months post enrollment
Title
Number of Participants Who Experienced Seven-day Point Prevalence of Smoking Abstinence
Description
Self-reported not smoking "even a puff" within the previous seven days, and exhaled carbon monoxide reading of <8 parts per million.
Time Frame
during the previous seven days at six months post baseline
Title
Median Number of Cigarettes Smoked Per Day During the Past Week
Description
Self-reported, median number of cigarettes per day during the previous seven days
Time Frame
during the previous seven days at six months post baseline
Title
Number of Participants Who Experienced Any Quit Attempts Since Enrollment
Description
Self-reported, smoke free for 24 hours or more since baseline (yes/no)
Time Frame
during the period between baseline and six months post-enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Enrolled in methadone treatment for at least three months Able to give informed consent Willing and able to participate in all study activities Smoked at least 100 cigarettes during their lifetime Currently smoke every day or most days Has access to a working telephone Interested in participating in a smoking cessation intervention and quitting smoking within the next six months Exclusion Criteria: Unable to speak English fluently Took smoking cessation related medication or participated in smoking cessation counseling in the past three months Pregnant or breastfeeding or planning on becoming pregnant or breastfeeding during the next six months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nina Cooperman, Psy.D.
Organizational Affiliation
Rutgers Robert Wood Johnson Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rutgers Robert Wood Johnson Medical School
City
New Brunswick
State/Province
New Jersey
ZIP/Postal Code
08901
Country
United States

12. IPD Sharing Statement

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Developing a Smoking Cessation Intervention for Methadone Maintained Smokers

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