Targeted Pharmacological and Behavioral Treatments for Smoking in Schizophrenia Study 1
Primary Purpose
Tobacco Dependence
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Varenicline
Placebo
Sponsored by
About this trial
This is an interventional basic science trial for Tobacco Dependence
Eligibility Criteria
Inclusion Criteria:
- Men and women
- Ages 18-65
- Have schizophrenia or schizoaffective disorder
- Would like to quit smoking within the next 6 months
- Have smoked at least 10 cigarettes per day in the past year
- Have breath CO level > 10 ppm
- Able to speak, read and comprehend English well enough to complete study procedures
Exclusion Criteria:
- Pregnant, breast-feeding, or unwilling to use medically-approved contraception
- Currently using varenicline, bupropion or nicotine replacement therapy for smoking cessation
- Medical disease that would preclude participation
- Unstable psychiatric conditions
- Body mass index (BMI) < 15 or > 38 kg/m2
- Past-month suicidal intention, with or without a specific plan
- Positive urine drug screen or breath alcohol level > 0.01% at screening
Sites / Locations
- Brown University, 121 South Main Street
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Varenicline
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Questionnaire on Smoking Urges - Brief Form
Average of all items, rated from 1 (strongly disagree) to 7 (strongly agree). Higher scores indicate higher levels of smoking urge or craving.
Minnesota Nicotine Withdrawal Scale - Negative Affect Scale
Average of responses to the anger, depression, anxiety and difficulty concentrating items, which are rated from 0 (not present) to 4 (severe).
Secondary Outcome Measures
Modified Cigarette Evaluation Questionnaire - Satisfaction Scale
Average of the satisfaction, taste and enjoyment items, which are rated from 1 (not at all) to 7 (extremely)
Modified Cigarette Evaluation Questionnaire - Reward Scale
Average of the calm, feel more awake, less irritable, help to concentrate and reduce hunger items, which are rated from 1 (not at all) to 7 (extremely)
Latency to Smoking Relapse
hours until relapse during a smoking abstinence period, verified with breath carbon monoxide (CO) levels
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03507127
Brief Title
Targeted Pharmacological and Behavioral Treatments for Smoking in Schizophrenia Study 1
Official Title
Targeted Pharmacological and Behavioral Treatments for Smoking in Schizophrenia Study 1
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Terminated
Why Stopped
Low rate of enrollment
Study Start Date
May 1, 2018 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brown University
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
Schizophrenia is associated with high rates of cigarette smoking and associated morbidity and mortality. In this study, smokers with schizophrenia will complete a baseline session and then randomized to varenicline (VAR) or placebo (PLA). After 1 week on medication, participants will complete a cigarette rating task session. Participants will then undergo a 72-hr abstinence period in which they will come to the laboratory twice per day and receive high-value cash reinforcement contingent upon meeting a strict breath CO abstinence criterion. At each visit, they will rate withdrawal symptoms, mood and craving. At the end of the abstinence period, they will repeat the cigarette rating task. Participants will return to the lab to provide a CO sample 24 hours later, and will text the lab with videos of their CO samples for one week. Date and time of smoking relapse will be measured from these samples.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Dependence
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Varenicline
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Varenicline
Intervention Description
Standard dosing: 0.5 mg/day on days 1-3, 0.5 mg twice daily (morning, evening) on days 4-7, then 1 mg twice daily to the end of the medication period.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Dosing schedule matched to active comparator: on tablet on days 1-3, one tablet twice daily (morning, evening) on days 4-7, then one tablet twice daily to the end of the medication period.
Primary Outcome Measure Information:
Title
Questionnaire on Smoking Urges - Brief Form
Description
Average of all items, rated from 1 (strongly disagree) to 7 (strongly agree). Higher scores indicate higher levels of smoking urge or craving.
Time Frame
72 hrs abstinence
Title
Minnesota Nicotine Withdrawal Scale - Negative Affect Scale
Description
Average of responses to the anger, depression, anxiety and difficulty concentrating items, which are rated from 0 (not present) to 4 (severe).
Time Frame
72 hrs abstinence
Secondary Outcome Measure Information:
Title
Modified Cigarette Evaluation Questionnaire - Satisfaction Scale
Description
Average of the satisfaction, taste and enjoyment items, which are rated from 1 (not at all) to 7 (extremely)
Time Frame
72 hrs abstinence
Title
Modified Cigarette Evaluation Questionnaire - Reward Scale
Description
Average of the calm, feel more awake, less irritable, help to concentrate and reduce hunger items, which are rated from 1 (not at all) to 7 (extremely)
Time Frame
72 hrs abstinence
Title
Latency to Smoking Relapse
Description
hours until relapse during a smoking abstinence period, verified with breath carbon monoxide (CO) levels
Time Frame
1 week
Other Pre-specified Outcome Measures:
Title
Brief Psychiatric Rating Scale
Description
Sum of all items rated from 1 (not present) to 7 (extremely severe)
Time Frame
72 hrs abstinence
10. Eligibility
Sex
All
Gender Based
Yes
Gender Eligibility Description
gender is based on self-report
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women
Ages 18-65
Have schizophrenia or schizoaffective disorder
Would like to quit smoking within the next 6 months
Have smoked at least 10 cigarettes per day in the past year
Have breath CO level > 10 ppm
Able to speak, read and comprehend English well enough to complete study procedures
Exclusion Criteria:
Pregnant, breast-feeding, or unwilling to use medically-approved contraception
Currently using varenicline, bupropion or nicotine replacement therapy for smoking cessation
Medical disease that would preclude participation
Unstable psychiatric conditions
Body mass index (BMI) < 15 or > 38 kg/m2
Past-month suicidal intention, with or without a specific plan
Positive urine drug screen or breath alcohol level > 0.01% at screening
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Tidey, PhD
Organizational Affiliation
Brown University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brown University, 121 South Main Street
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02912
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Targeted Pharmacological and Behavioral Treatments for Smoking in Schizophrenia Study 1
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