Pioglitazone as an Adjunct to Cognitive-Behavioral Therapy for Cocaine Relapse Prevention
Primary Purpose
Cocaine Use Disorder
Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cognitive Behavioral Therapy (CBT)
Pioglitazone
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Cocaine Use Disorder focused on measuring Cocaine Use, Cocaine Addiction, Cognitive Behavioral Therapy, Relapse Prevention
Eligibility Criteria
Inclusion Criteria:
- 18 to 60 years old
- meet DSM 5 diagnostic criteria for cocaine use disorder
- report recent cocaine use, verified by at least one positive urine drug screen for the cocaine metabolite, benzoylecgonine, during intake
- be judged by the medical staff to be psychiatrically stable and physically healthy
- for females, be using an effective form of birth control (e.g., barrier, IUD, or sterilization) and not be pregnant as determined by a serum pregnancy test at screening and negative urine pregnancy test at intake prior to first dose of investigational drug (test will be repeated weekly to ensure that female patients do not continue in the study if pregnant) or lactating
- be willing to be admitted to a 5-day inpatient detoxification program at The Right Step Houston
- be able to understand the consent form and provide written informed consent
- be able to provide the names of at least 2 persons who can consistently locate their whereabouts
Exclusion Criteria:
- have an acute medical or psychiatric disorder that would, in the judgment of the study physician, make participation difficult or unsafe
- have suicidal or homicidal ideation that requires immediate attention
- have another current (≥ moderate) substance use disorder aside from alcohol, nicotine, or marijuana
- have a medical condition contraindicating PIO pharmacotherapy (e.g., drug- or insulin-dependent diabetes, congestive heart failure, edema, clinical significant liver disease, hypoglycemia, history of bladder cancer) or be taking medications that would adversely interact with PIO (e.g., CYP2C8 inhibitors or inducers, antihyperglycemic medications)
- be concurrently enrolled in other addiction treatment services aside from smoking cessation
- if female, be currently pregnant, breastfeeding, or planning on conception
- have conditions of probation or parole requiring reports of drug use to officers of the court
- be unable to read, write, or speak English
- be homeless (live on the street)
- have medical contraindications to MRI/DTI scans (e.g., history of pacemaker, metal implants, or welding/metal work without protective eyewear)
Sites / Locations
- UTHealth Center for Neurobehavioral Research on AddictionRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
CBT + pioglitazone
CBT + placebo
Arm Description
Cognitive Behavioral Therapy will be administered twice weekly during weeks 1-4 and once weekly during weeks 5-12 and augmented with a pioglitazone (45 mg) capsule every day during weeks 1-12.
Cognitive Behavioral Therapy will be administered twice weekly during weeks 1-4 and once weekly during weeks 5-12 and augmented with a placebo capsule every day during weeks 1-12.
Outcomes
Primary Outcome Measures
Change in white matter integrity as assessed by change in fractional anisotropy value measured by diffusion tensor imaging
Anisotropy values range from 0 to 1, where a higher value indicates greater white matter integrity.
Change in white matter integrity as assessed by change in radial diffusivity value measured by diffusion tensor imaging
Radial diffusivity (RD) values are not bound by specified upper and lower ranges, as the metric is a derivation of two diffusion eigenvalues = ([lambda2 / lambda3] / 2). Higher RD values are indicative of decreased white matter integrity as related to myelin integrity; conversely lower RD scores indicate better white matter integrity.
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Number of participants who don't relapse as assessed by continuous cocaine-negative urine drug screens in the final three weeks of treatment
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Self-reported craving for cocaine as assessed by average Brief Substance Craving Scale score across 12 weeks of treatment
The Brief Substance Craving Scale (BSCS) score ranges from 0 to 4, with a higher score indicating greater craving. Participants will be assessed by BSCS once per week for 12 weeks, and the average BSCS score over the 12 weeks will be reported.
Self-reported craving for cocaine as assessed by average Visual Analogue Scale score across 12 weeks of treatment
The Visual Analogue Scale (VAS) score ranges from 0 to 100, with a higher score indicating greater craving. Participants will be assessed by VAS once per week for 12 weeks, and the average VAS score over the 12 weeks will be reported.
Secondary Outcome Measures
Total percentage of days abstinent during treatment as assessed by self-reported non-use days confirmed by cocaine-negative urine drug screen results
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Total percentage of cocaine-negative urine drug screens during treatment as assessed by number of cocaine-negative samples out of total number of urine samples provided
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Full Information
NCT ID
NCT04843046
First Posted
April 8, 2021
Last Updated
May 23, 2023
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Institute on Drug Abuse (NIDA)
1. Study Identification
Unique Protocol Identification Number
NCT04843046
Brief Title
Pioglitazone as an Adjunct to Cognitive-Behavioral Therapy for Cocaine Relapse Prevention
Official Title
Pioglitazone as an Adjunct to Cognitive-Behavioral Therapy for Cocaine Relapse Prevention
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 23, 2021 (Actual)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
August 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Institute on Drug Abuse (NIDA)
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.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to see how well pioglitazone, when used with cognitive behavioral therapy, works at helping people who have recently stopped using cocaine to continue to not use cocaine.
Detailed Description
Over one million American adults suffer from cocaine use disorder (CUD) with recent trends showing an increase in cocaine-related deaths since 2010. For the chronic cocaine user, significant changes in brain function and structure set the stage for relapse that, unfortunately, continues to be the most common outcome following treatment. For substance use disorders, cognitive-behavioral therapy (CBT) is arguably the most empirically supported and widely used relapse prevention approach. Considered to be a cognitive control therapy, CBT aims to improve 'top-down' executive control functions that are impaired in CUD and strongly connected to relapse. Converging evidence suggests that CBT promotes meaningful changes in brain regions associated with cognitive control. Still, many patients with cognitive impairments show suboptimal response to CBT, bolstering the call for research aimed at improving effects with integrative treatments.
The goal of this project is to enhance the relapse-prevention effects of CBT with adjunctive use of pioglitazone (PIO), a peroxisome proliferator-activated receptor gamma (PPAR-γ) agonist. Unlike traditional medications that target classic neurotransmitter systems, PIO's activation of the PPAR pathway confers broad spectrum anti-inflammatory and neuroprotective effects against insult to brain white matter (WM). The functional significance of WM in CUD has been well established by evidence showing that: (1) chronic cocaine exposure alters WM structural integrity; (2) WM alterations compromise cognitive function in CUD; and (2) better WM integrity predicts better CUD treatment outcome. In a recent proof of concept trial it was found that PIO significantly improved brain WM integrity in a small sample of non-abstinent patients with CUD. Treatment with PIO was well-tolerated and associated with reduced cocaine craving relative to placebo. Collectively, these findings raise the exciting possibility that PIO may augment responding to CBT via improved neural structure and cognitive function.
A randomized double-blind clinical trial will be utilized to evaluate the efficacy of CBT with adjunctive PIO in recently abstinent patients during the early phase of recovery when craving is prominent, relapse risk is high, and intact cognitive control is required to actively maintain abstinence. Upon completion of a 5-day inpatient detoxification, 60 adults with CUD will complete titration to full dose of randomized medication, either PIO (45mg daily) or placebo, and begin 12 weeks of outpatient CBT treatment while continuing to receive study medication. Specific aims will examine the effects of PIO on targeted mechanisms of change (WM integrity, cognitive function, cocaine craving) and demonstrate evidence linking clinical efficacy (abstinence, functional health) with mechanism engagement. Expected results will establish PIO as an adjunctive treatment that can be integrated with CBT to reduce relapse risk following detoxification, thereby meeting NIDA's strategic priority of evaluating the use of medications to improve the efficacy of behavioral interventions (PA-18-055).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine Use Disorder
Keywords
Cocaine Use, Cocaine Addiction, Cognitive Behavioral Therapy, Relapse Prevention
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CBT + pioglitazone
Arm Type
Active Comparator
Arm Description
Cognitive Behavioral Therapy will be administered twice weekly during weeks 1-4 and once weekly during weeks 5-12 and augmented with a pioglitazone (45 mg) capsule every day during weeks 1-12.
Arm Title
CBT + placebo
Arm Type
Placebo Comparator
Arm Description
Cognitive Behavioral Therapy will be administered twice weekly during weeks 1-4 and once weekly during weeks 5-12 and augmented with a placebo capsule every day during weeks 1-12.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavioral Therapy (CBT)
Other Intervention Name(s)
CBT
Intervention Description
All participants will receive evidence-based individual Cognitive Behavioral Therapy (CBT) shown to be an effective intervention for maintaining abstinence following detoxification. Trained masters-level licensed professional counselors will deliver CBT.
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Other Intervention Name(s)
Actos
Intervention Description
Pioglitazone capsules will start at 30 mg (Detox days 3 and 4) and increase to fixed dose of 45 mg for study weeks 1-12 and will also contain riboflavin.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Corn Starch
Intervention Description
Placebo capsules will be filled with corn starch and riboflavin.
Primary Outcome Measure Information:
Title
Change in white matter integrity as assessed by change in fractional anisotropy value measured by diffusion tensor imaging
Description
Anisotropy values range from 0 to 1, where a higher value indicates greater white matter integrity.
Time Frame
Week 0 and Week 12
Title
Change in white matter integrity as assessed by change in radial diffusivity value measured by diffusion tensor imaging
Description
Radial diffusivity (RD) values are not bound by specified upper and lower ranges, as the metric is a derivation of two diffusion eigenvalues = ([lambda2 / lambda3] / 2). Higher RD values are indicative of decreased white matter integrity as related to myelin integrity; conversely lower RD scores indicate better white matter integrity.
Time Frame
Week 0 and Week 12
Title
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
Description
The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Time Frame
Week 0
Title
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
Description
The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Time Frame
Week 4
Title
Change in working memory as assessed by the NIH Toolbox Cognition Battery List Sorting Task
Description
The List Sorting Task has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Time Frame
Week 12
Title
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
Description
The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Time Frame
Week 0
Title
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
Description
The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Time Frame
Week 4
Title
Change in attention/impulsivity as assessed by the NIH Toolbox Cognition Battery Flanker Test
Description
The Flanker Test has an age-adjusted scale score that ranges from 0 to 100, with a higher score indicating better performance.
Time Frame
Week 12
Title
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
Description
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Time Frame
Week 0
Title
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
Description
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Time Frame
Week 4
Title
Change in cognitive function as assessed by the NIH Toolbox Cognition Battery Fluid Cognition Composite score
Description
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Time Frame
Week 12
Title
Number of participants who don't relapse as assessed by continuous cocaine-negative urine drug screens in the final three weeks of treatment
Description
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Time Frame
From Week 10 to Week 12
Title
Self-reported craving for cocaine as assessed by average Brief Substance Craving Scale score across 12 weeks of treatment
Description
The Brief Substance Craving Scale (BSCS) score ranges from 0 to 4, with a higher score indicating greater craving. Participants will be assessed by BSCS once per week for 12 weeks, and the average BSCS score over the 12 weeks will be reported.
Time Frame
From Week 1 to Week 12
Title
Self-reported craving for cocaine as assessed by average Visual Analogue Scale score across 12 weeks of treatment
Description
The Visual Analogue Scale (VAS) score ranges from 0 to 100, with a higher score indicating greater craving. Participants will be assessed by VAS once per week for 12 weeks, and the average VAS score over the 12 weeks will be reported.
Time Frame
From Week 1 to Week 12
Secondary Outcome Measure Information:
Title
Total percentage of days abstinent during treatment as assessed by self-reported non-use days confirmed by cocaine-negative urine drug screen results
Description
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Time Frame
From Week 1 to Week 12
Title
Total percentage of cocaine-negative urine drug screens during treatment as assessed by number of cocaine-negative samples out of total number of urine samples provided
Description
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Time Frame
From Week 1 to Week 12
Title
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
Description
The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Time Frame
Week 0
Title
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
Description
The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Time Frame
Week 4
Title
Functional health status as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) global health summary score
Description
The PROMIS global health summary score is a T-score derived from the global physical health (GPH) and global mental health (GMH) items and ranges from 40 to 60, with a greater T-score indicating better functional health status.
Time Frame
Week 12
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:
18 to 65 years old
meet DSM 5 diagnostic criteria for cocaine use disorder
report recent cocaine use, verified by at least one positive urine drug screen for the cocaine metabolite, benzoylecgonine, during intake
be judged by the medical staff to be psychiatrically stable and physically healthy
for females, be using an effective form of birth control (e.g., barrier, IUD, or sterilization) and not be pregnant as determined by a serum pregnancy test at screening and negative urine pregnancy test at intake prior to first dose of investigational drug (test will be repeated weekly to ensure that female patients do not continue in the study if pregnant) or lactating
be willing to be admitted to a 5-day inpatient detoxification program at The Right Step Houston
be able to understand the consent form and provide written informed consent
be able to provide the names of at least 2 persons who can consistently locate their whereabouts
Exclusion Criteria:
have an acute medical or psychiatric disorder that would, in the judgment of the study physician, make participation difficult or unsafe
have suicidal or homicidal ideation that requires immediate attention
have another current (≥ moderate) substance use disorder aside from alcohol, nicotine, or marijuana
have a medical condition contraindicating PIO pharmacotherapy (e.g., drug- or insulin-dependent diabetes, congestive heart failure, edema, clinical significant liver disease, hypoglycemia, history of bladder cancer) or be taking medications that would adversely interact with PIO (e.g., CYP2C8 inhibitors or inducers, antihyperglycemic medications)
be concurrently enrolled in other addiction treatment services aside from smoking cessation
if female, be currently pregnant, breastfeeding, or planning on conception
have conditions of probation or parole requiring reports of drug use to officers of the court
be unable to read, write, or speak English
be homeless (live on the street)
have medical contraindications to MRI/DTI scans (e.g., history of pacemaker, metal implants, or welding/metal work without protective eyewear)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joy M Schmitz, PhD
Phone
713-486-2867
Email
Joy.M.Schmitz@uth.tmc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jessica N Vincent, BS
Phone
713-486-2803
Email
Jessica.N.Vincent@uth.tmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joy M Schmitz, PhD
Organizational Affiliation
UT Houston
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Scott D Lane, PhD
Organizational Affiliation
UT Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
UTHealth Center for Neurobehavioral Research on Addiction
City
Houston
State/Province
Texas
ZIP/Postal Code
77054
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joy M Schmitz, PhD
Phone
713-486-2867
Email
Joy.M.Schmitz@uth.tmc.edu
First Name & Middle Initial & Last Name & Degree
Joy M Schmitz, Ph.D.
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Pioglitazone as an Adjunct to Cognitive-Behavioral Therapy for Cocaine Relapse Prevention
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