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CompletedNCT00344565Updated Dec 3, 2012

A Placebo-Controlled Double-Blind Combined Treatment of Modafinil and CBT for Cocaine Dependence

A Phase 2 interventional study of Modafinil and Cognitive Behavioral Therapy--Relapse Prevention in Cocaine Dependence, sponsored by Research Foundation for Mental Hygiene, Inc.. Completed. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2012-12-03.

Sponsored by Research Foundation for Mental Hygiene, Inc. · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

The purpose of this study is to test whether a cognitive behavioral therapy (CBT) and a medication called modafinil, which is approved to treat sleep disorders, will help individuals who are abusing cocaine.

Read the detailed description

Chronic cocaine abuse has been documented to produce cognitive impairments in various domains. The observed cognitive deficits in the substance abuse population include, but are not restricted to, attention, concentration, verbal and nonverbal memory, problem solving and abstract reasoning. Our recent studies (IRB Protocol # 3998) demonstrated that in cocaine dependent participants such cognitive deficits have been shown to: 1) negatively effect retention and 2) impede the ability of the drug abuser to benefit from cognitive behavioral therapy- relapse prevention (CBT-RP) that requires participant to attend to novel stimuli, integrate new information with existing stores, and translate information into behavior change (Aharonovich, Hasin \& Nunes, 2003; Aharonovich et al, in press). Furthermore, the toxic effects of cocaine together with withdrawal symptoms, such as fatigue and hypersomnia make it difficult to fully engage in any psychosocial intervention including CBT-RP.

Recent findings indicate that cocaine dysregulates reward-related glutamate pathways (Dackis \& O'Brien, 2003; Kalivas et al, 2003). Modafinil is a medication known to improve attention, increase wakefulness, energy, and alertness in part by increasing glutamate levels. In light of this work and the negative affect of cognitive impairments on treatment outcomes, testing cognitive enhancing medications that act on glutamate pathways is a novel promising strategy for improving treatment for cocaine dependence. Modafinil is approved for sleep disorders and is a relatively safe medication for cocaine-dependent participants as it has a low abuse potential and has shown promise in a double blind placebo controlled trial for cocaine dependence (Rush et al, 2002; Jasinski, 2000, Dackis et al, 2005). We therefore propose a double blind placebo controlled 12-week exploratory pilot study of modafinil, a "wakefulness agent," in conjunction with sessions of CBT-RP enhanced with motivational interviewing components.

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Conditions studied

  • Cocaine Dependence
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In context

Cocaine-Related Disorders

415 studies on the registry are indexed under Cocaine-Related Disorders; 12 are open to participants now.

This study's enrollment of 15 is below the median of 60 across 312 interventional studies indexed under Cocaine-Related Disorders.

Browse Cocaine-Related Disorders studies →

Lead sponsor

Research Foundation for Mental Hygiene, Inc. is the lead sponsor of 35 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Meets DSM IV criteria for current cocaine dependence and is seeking treatment.
  • Used cocaine at least eight days in the past month or reports episodic binges of large amounts of cocaine (at least $150 worth) at least twice per month
  • Able to give informed consent and comply with study procedures.

Exclusion criteria

Exclusion Criteria:

  • Meets DSM IV criteria for current mood disorder or past or current mania (i.e. bipolar disorder), schizophrenia or any psychotic disorder other than transient psychosis due to drug abuse.
  • Baseline 21 item Hamilton Depression Scale scores ≥ 15
  • History of seizures
  • Chronic organic mental disorder.
  • Significant current suicidal risk.
  • Pregnancy, lactation, or failure in sexually active female participants to use adequate contraceptive methods.
  • Unstable physical disorders, which might make participation hazardous such as hypertension, hepatitis, participants with mildly elevated AST and ALT levels (\< 3 X upper limit or normal are acceptable), or diabetes.
  • Coronary vascular disease as indicated by history, or suspected by abnormal EKG or history of cardiac symptoms.
  • Current use of prescribed psychotropic medications.
  • Current use of medications that interact with modafinil: Tricyclic anti-depressants; MOA Inhibitors; diazepam; phenytoin and medications containing Ethinyl Estradiol
  • Known hypersensitivity to modafinil
  • Currently meets DSM-IV criteria for narcolepsy
  • Currently meets DSM-IV criteria for ADHD
  • Currently meets DSM-IV criteria for opioid or sedative-hypnotic dependence.
  • Currently meets criteria for DSM-IV alcohol dependence with evidence of clinically significant physiological dependence in need of medically supervised detoxification.
  • Current cannabis dependence is identified as the main problem-i.e. participants with current DSM-IV cannabis dependence are eligible, as long as cocaine is identified by the participant as the primary substance problem for which they are seeking treatment.
  • Gross visual or auditory impairments
  • First language is not English and received NO formal education in English-speaking school
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
15 participants (actual)

Study arms

  • Placebo comparator
    Placebo

    Placebo, was matched to modafinil up to 400 mg/day. Patients also receive motivational interviewing and Cognitive Behavioral Therapy-Relapse Prevention (CBT-RP)

    Drug: Modafinil · Behavioral: Cognitive Behavioral Therapy--Relapse Prevention

  • Active comparator
    Modafinil

    Modafinil (Active comparator). Patients received motivational interviewing and Cognitive Behavioral Therapy--relapse prevention (CBT-RP)

    Drug: Modafinil · Behavioral: Cognitive Behavioral Therapy--Relapse Prevention

Interventions

  • DrugModafinil

    During the first lead-in week, participants will attend the clinic 3 times per week, participate in one session of neuropsychological assessment and receive motivational interviewing and Cognitive Behavioral Therapy--Relapse Prevention (CBT-RP). At the end of the first lead-in week participants will be randomized to modafinil or placebo stratified by the levels of cocaine use, and whether or not abstinence was achieved. Participants will then be followed for 11 weeks with measures of cocaine cravings and withdrawal, and drug use outcome, and will receive CBT-RP.

    Also known as: Provigil

  • BehavioralCognitive Behavioral Therapy--Relapse Prevention

    Once weekly individual session of motivational interviewing and Cognitive Behavioral Therapy--Relapse Prevention (CBT-RP)

    Also known as: CBT-RP

06

What researchers measure

Primary outcomes

  1. Cocaine use outcome at week 12 (measured with urine toxicology and self-reports)

    Time frame: At week 12

Secondary outcomes

  1. Cognitive functioning at week 12 (measured with neuropsychological assessment)

    Time frame: At week 12

  2. Cocaine withdrawal symptoms throughout (measured with clinical assessments and self-reports)

    Time frame: At week 12

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Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 3, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00344565
Lead sponsor
Research Foundation for Mental Hygiene, Inc.
Collaborators
National Institute on Drug Abuse (NIDA)
Responsible party
Efrat Aharonovich (Research Scientist, Research Foundation for Mental Hygiene, Inc.) — Principal investigator
First posted
Jun 27, 2006
Start date
Nov 2005
Primary completion
Dec 2006
Completion
Mar 2007
Last update
Dec 3, 2012

Study contacts

Efrat Aharonovich, PhD
principal investigator · Columbia University - New York State Psychiatric Institute

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2012. You cannot join it, but the record below documents what was studied.

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