Skip to content

Improving Learning-based Treatment of Cocaine Dependence With Medication

Improving Learning-based Treatment of Cocaine Dependence With Medication

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01526538
Enrollment
52
Registered
2012-02-06
Start date
2011-09-30
Completion date
2013-03-31
Last updated
2017-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COCAINE-RELATED DISORDERS

Brief summary

This study will test the efficacy of d-cycloserine in enhancing response to learning-based treatment for cocaine dependence, specifically contingency management.

Detailed description

Cocaine dependence is a public health problem with substantial morbidity, however no effective pharmacotherapy for cocaine dependence has been approved by the FDA. Unlike previous medication studies that have sought to pharmacologically reduce cocaine reinforcement, seeking or craving, this exploratory clinical trial will test d-cycloserine (DCS) for its ability to improve learning-based behavioral treatment of cocaine dependence. DCS is an NMDA partial agonist that has been shown to robustly improve learning in preclinical models, including extinction of cocaine conditioned place preference and blockade of cocaine reacquisition, and to improve extinction-learning based exposure therapy for multiple anxiety disorders. This Phase II clinical trial will investigate the pharmacological (DCS) enhancement of a behavioral treatment combining contingency management (CM) and novel home-environment exposure therapy sessions for cocaine dependence. High magnitude CM incentives will be used to promote the cocaine abstinence necessary for extinction in home-based exposure sessions. Participants will be randomized into 2 groups: 1. CM with placebo (CM+PL), and 2. CM with DCS (CM+DCS). For 19 days after group assignment, participants will report to the laboratory 3 times per week (Mon, Wed, Fri) to provide urine samples, receive contingent vouchers, and complete assessments of drug use, craving, mood, withdrawal, and quit self-efficacy. DCS (50 mg) or placebo will be administered on Mon, Wed and Fri study visits (at the end of the lab visit before returning to the home environment for exposure sessions during the time of DCS action). Follow-up visits will be conducted at 1 week, 1 month, and 3 months post-CM completion, during which time measures of drug use (self-reported and urinalysis), craving, mood, and withdrawal will be obtained. Comparison of continuous abstinence post-CM between the groups will be the primary outcome measure. During an initial laboratory session, a battery of learning/cognitive tasks will test for forms of learning/cognition enhanced by DCS that might contribute to the treatment effect. This project will test the efficacy of a novel intervention for cocaine dependence that was developed based on a known efficacious cocaine dependence treatment (CM), principles of extinction learning theory, and a medication shown to improve preclinical learning in general, including extinction of cocaine conditioning, and clinical learning-based exposure treatment of anxiety disorders. The study may indicate cost effective additions (home exposure sessions and DCS) to extend CM benefit after the removal of contingencies, and therefore may increase the dissemination of CM in community settings.

Interventions

DRUGd-cycloserine

50 mg d-cycloserine

DRUGsugar pill

placebo

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-60 years of age (\> 60 due to age-related effects on cognitive functioning) * Satisfy DSM-IV criteria for cocaine dependence (primarily crack) * Able to complete all study measures * Currently seeking treatment for cocaine dependence

Exclusion criteria

* Meets DSM-IV criteria for dependence on a drug other than cocaine or nicotine (may meet abuse criteria for other drugs) * Pregnant, breast feeding, or planning to become pregnant within 3 months * If female, do not agree to use an effective means of birth control during the course of treatment (via phone screen) * History of seizure disorder, severe hepatic impairment, porphyria, serious head trauma, dementia, or significant cognitive impairment * Diagnosis of current major psychiatric disorder besides substance dependence or abuse * Reported use of DCS in the past year * Illiteracy, as will be determined during in-person screening * Concurrently prescribed or using ethionamide or isoniazid (both used to treat tuberculosis) * Positive urine result for opioids at screening interview

Design outcomes

Primary

MeasureTime frameDescription
Urinalysis Benzoylecgonine (Cocaine Metabolite)(ng/ml)1 month post-treatmentThe primary outcome for this study will be post-treatment continuous abstinence, as assessed by urinalysis results
Medication Side-effects1 month post-treatment.self-report of medication side effects (Units of Measure is the count of specific reported effects)

Secondary

MeasureTime frame
Learning Task by Itami and UnoAt the baseline laboratory visit

Countries

United States

Participant flow

Participants by arm

ArmCount
50 mg D-cycloserine
active drug condition d-cycloserine: 50 mg d-cycloserine
21
Sugar Pill
Inactive placebo sugar pill: placebo
18
Total39

Baseline characteristics

Characteristic50 mg D-cycloserineSugar PillTotal
Age, Continuous51.3 years
STANDARD_DEVIATION 5.3
52.1 years
STANDARD_DEVIATION 4.9
51.7 years
STANDARD_DEVIATION 5.1
Gender
Female
6 Participants6 Participants12 Participants
Gender
Male
15 Participants12 Participants27 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 210 / 18
serious
Total, serious adverse events
0 / 210 / 18

Outcome results

Primary

Medication Side-effects

self-report of medication side effects (Units of Measure is the count of specific reported effects)

Time frame: 1 month post-treatment.

ArmMeasureValue (NUMBER)
50 mg D-cycloserineMedication Side-effects0 Adverse event reports
Sugar PillMedication Side-effects0 Adverse event reports
Primary

Urinalysis Benzoylecgonine (Cocaine Metabolite)(ng/ml)

The primary outcome for this study will be post-treatment continuous abstinence, as assessed by urinalysis results

Time frame: 1 month post-treatment

ArmMeasureValue (MEAN)Dispersion
50 mg D-cycloserineUrinalysis Benzoylecgonine (Cocaine Metabolite)(ng/ml)36.7 ng/mlStandard Deviation 7.7
Sugar PillUrinalysis Benzoylecgonine (Cocaine Metabolite)(ng/ml)32.4 ng/mlStandard Deviation 6.6
Secondary

Learning Task by Itami and Uno

Time frame: At the baseline laboratory visit

ArmMeasureValue (MEAN)Dispersion
50 mg D-cycloserineLearning Task by Itami and Uno81.5 % correctStandard Error 3.5
Sugar PillLearning Task by Itami and Uno72.9 % correctStandard Error 4.4

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026