UTHealth Center for Neurobehavioral Research on Addiction
Houston, Texas, 77054, United States
NCT Number: NCT04843046
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.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Houston, Texas, 77054, United States
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).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Other names: CBT
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.
Other names: Actos
Placebo capsules will be filled with corn starch and riboflavin.
Other names: Corn Starch
Time frame: Week 0 and Week 12
Anisotropy values range from 0 to 1, where a higher value indicates greater white matter integrity.
Time frame: Week 0 and Week 12
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
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
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
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
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
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
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
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
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
The Fluid Cognition Composite score is the normed standardized score ranging from 0 to 145, with a higher score indicating better performance.
Time frame: From Week 10 to Week 12
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Time frame: From Week 1 to Week 12
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
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
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Time frame: From Week 1 to Week 12
For a cocaine-negative urine drug screen result, benzoylecgonine levels must be under 150 ng/mL.
Time frame: Week 0
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
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
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.
The University of Texas Health Science Center, Houston
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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