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Treating Schizophrenic Smokers: Effects on Craving, Cues and Withdrawal

Primary Purpose

Tobacco Use Disorder

Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
varenicline
Adaptation of Motivational Interviewing
Sponsored by
VA Boston Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tobacco Use Disorder focused on measuring smoking cessation, varenicline, schizophrenia, serious mental illness, Nicotine addiction, Smoking Behavior

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Eligible participants for this study:

  • Are between the ages 18-65 years of age
  • Are daily cigarette smokers
  • Have smoked a minimum of 10 cigarettes per day for at least one year
  • Are confirmed smokers as verified by CO
  • Have a psychiatric diagnosis of schizophrenia or schizoaffective disorder (any subtype) as determined by the SCID-IV. Participants must have received a stable dose of antipsychotic medication for at least 2 weeks prior to beginning the study. Patients receiving clozapine at 500 mg/day or more must also be receiving anti-seizure prophylaxis. Patients must be determined to be psychiatrically stable at baseline as established by standardized interview and medical review by psychiatrist.

Exclusion Criteria:

Individuals who are not eligible to participate in this study include individuals with:

  • Any serious or unstable medical problem in the last 6 months
  • Severe renal impairment
  • A history of clinically significant allergic reactions to nicotine agonist medications
  • Current primary use of tobacco products other than cigarettes
  • Breath alcohol level > 0.005 g/l at screening
  • Current substance abuse or dependence (besides nicotine)
  • Current attempts to quit smoking using any method
  • Designation as legally incompetent to sign the informed consent (i.e., have a guardian or have delegated power of attorney to another).

Other exclusions are:

  • Current use of medications that might affect the behavioral response to cigarette smoking, including transdermal nicotine or nicotine gum and bupropion - Inability to participate in the screening session due to severe psychosis, severe depression or suicidality, current mania, or an organic mental disorder such as dementia or delirium
  • Presence of unstable psychiatric symptoms or clinical deterioration (i.e., unstable psychosis, homicidality, or suicidality) within the last month.
  • Females of childbearing potential are eligible if not pregnant or nursing and if they practice effective contraception (oral, injectable, or implantable contraceptives; intrauterine device; or barrier method with spermicide).
  • There currently are no known contraindications to the use of varenicline and no identified drug-drug interactions. However, reduced dosage of varenicline is recommended for individuals with severe renal impairment.

Sites / Locations

  • VA Boston Healthcare System Brockton Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

VAR-MI: This group will receive 1mg/day varenicline (titrated from .5mg/day) and two sessions of a motivational interviewing platform CBT treatment over the course of two weeks.

PLA-MI: VAR-MI: This group will receive a daily placebo pill and two sessions of a motivational interviewing platform CBT treatment over the course of two weeks.

Outcomes

Primary Outcome Measures

Reported Smoking Urge and Withdrawal

Secondary Outcome Measures

Smoking Status
Mood Ratings

Full Information

First Posted
October 28, 2008
Last Updated
June 3, 2015
Sponsor
VA Boston Healthcare System
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1. Study Identification

Unique Protocol Identification Number
NCT00781755
Brief Title
Treating Schizophrenic Smokers: Effects on Craving, Cues and Withdrawal
Official Title
Phase 4 Study of Treating Schizophrenic Smokers Using Varenicline and Behavioral Intervention: Effects on Craving, Cues and Withdrawal
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Withdrawn
Why Stopped
Study design was altered such that a treatment component was removed through the VA IRB. We did not and will not begin this clinical trial.
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
VA Boston Healthcare System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a clinical research protocol to study the efficacy of combined varenicline (Chantix) and motivational interviewing (MI) for smoking cessation in a sample of smokers who have been diagnosed with schizophrenia or schizoaffective disorder. The study is a double-blind, randomized, controlled, subacute treatment trial of MI plus varenicline (VAR-MI) versus MI plus placebo (PLA-MI). The pharmaceutical treatment will utilize Chantix at a dose of 1 mg/day for a period of two weeks. The primary goal is to determine if VAR-MI decreases baseline behavioral measures of urge and withdrawal and reduces baseline rates of cigarette consumption. The primary efficacy measures of VAR-MI vs. PLA-MI treatment are: Minnesota Nicotine Withdrawal Scale, Questionnaire for Smoking Urge-brief, number of cigarettes smoked per day in the previous week, CO levels, and Brief Psychiatric Rating Scale and Positive And Negative Symptom Scale scores on the last day of the study. Other primary outcome measures are to determine the effects of VAR-MI and PLA-MI on smoking cue-induced urges in tobacco cue reactivity sessions and reward responsiveness as assessed by a computerized task.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Disorder
Keywords
smoking cessation, varenicline, schizophrenia, serious mental illness, Nicotine addiction, Smoking Behavior

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
VAR-MI: This group will receive 1mg/day varenicline (titrated from .5mg/day) and two sessions of a motivational interviewing platform CBT treatment over the course of two weeks.
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
PLA-MI: VAR-MI: This group will receive a daily placebo pill and two sessions of a motivational interviewing platform CBT treatment over the course of two weeks.
Intervention Type
Drug
Intervention Name(s)
varenicline
Intervention Description
.5mg/day for 3 days then titrated to 1.0mg/day for 11 days. A total dosing regimen of 14 days.
Intervention Type
Behavioral
Intervention Name(s)
Adaptation of Motivational Interviewing
Intervention Description
2 sessions of behavioral intervention designed to create ambivalence about quitting or plan for a quit attempt if the patient is ready.
Primary Outcome Measure Information:
Title
Reported Smoking Urge and Withdrawal
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Smoking Status
Time Frame
2 weeks
Title
Mood Ratings
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eligible participants for this study: Are between the ages 18-65 years of age Are daily cigarette smokers Have smoked a minimum of 10 cigarettes per day for at least one year Are confirmed smokers as verified by CO Have a psychiatric diagnosis of schizophrenia or schizoaffective disorder (any subtype) as determined by the SCID-IV. Participants must have received a stable dose of antipsychotic medication for at least 2 weeks prior to beginning the study. Patients receiving clozapine at 500 mg/day or more must also be receiving anti-seizure prophylaxis. Patients must be determined to be psychiatrically stable at baseline as established by standardized interview and medical review by psychiatrist. Exclusion Criteria: Individuals who are not eligible to participate in this study include individuals with: Any serious or unstable medical problem in the last 6 months Severe renal impairment A history of clinically significant allergic reactions to nicotine agonist medications Current primary use of tobacco products other than cigarettes Breath alcohol level > 0.005 g/l at screening Current substance abuse or dependence (besides nicotine) Current attempts to quit smoking using any method Designation as legally incompetent to sign the informed consent (i.e., have a guardian or have delegated power of attorney to another). Other exclusions are: Current use of medications that might affect the behavioral response to cigarette smoking, including transdermal nicotine or nicotine gum and bupropion - Inability to participate in the screening session due to severe psychosis, severe depression or suicidality, current mania, or an organic mental disorder such as dementia or delirium Presence of unstable psychiatric symptoms or clinical deterioration (i.e., unstable psychosis, homicidality, or suicidality) within the last month. Females of childbearing potential are eligible if not pregnant or nursing and if they practice effective contraception (oral, injectable, or implantable contraceptives; intrauterine device; or barrier method with spermicide). There currently are no known contraindications to the use of varenicline and no identified drug-drug interactions. However, reduced dosage of varenicline is recommended for individuals with severe renal impairment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary B Kaplan, M.D.
Organizational Affiliation
VA Boston Healthcare System
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Suzy Bird Gulliver, Ph.D.
Organizational Affiliation
VISN 17 Center of Excellence for Research on Returning War Veterans
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Barbara W Kamholz, Ph.D.
Organizational Affiliation
VA Boston Healthcare System
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
James Levitt, M.D.
Organizational Affiliation
VA Boston Healthcare System
Official's Role
Study Chair
Facility Information:
Facility Name
VA Boston Healthcare System Brockton Medical Center
City
Brockton
State/Province
Massachusetts
ZIP/Postal Code
02301
Country
United States

12. IPD Sharing Statement

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Treating Schizophrenic Smokers: Effects on Craving, Cues and Withdrawal

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