Modafinil, Sleep, and Cognition in Cocaine Dependence
Information source: National Institute on Drug Abuse (NIDA)
Information obtained from ClinicalTrials.gov on August 08, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Cocaine Dependence; Substance-Induced Sleep Disorder; Substance-Induced Cognitive Disorder
Intervention: Modafinil (Drug); Placebo (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: National Institute on Drug Abuse (NIDA) Official(s) and/or principal investigator(s): Peter T Morgan, MD, PhD, Principal Investigator, Affiliation: Yale University
Overall contact: Peter Morgan, MD, PhD, Phone: 203-974-7515, Email: peter.morgan@yale.edu
Summary
Subjects participating in this protocol will participate in three phases: 1) pre-admission,
2) inpatient admission, and 3) follow-up. Pre-admission involves screening (detailed in
inclusion/exclusion criteria section) and one week of outpatient sleep and activity
monitoring. Inpatient admission is 16 consecutive nights on the Clinical Neuroscience
Research Unit and involves subjective and objective tests of sleep, sleepiness, attention,
and learning. During inpatient admission subjects will take modafinil or placebo. For
follow-up, subjects will return to the CNRU for one night and again participate in objective
tests of sleep, sleepiness, attention, and learning. We hypothesize that modafinil will
decrease subject and objective measures of sleepiness and will promote attention and learning
in cocaine dependent persons.
Clinical Details
Official title: Modafinil, Sleep, and Cognition in Cocaine Dependence
Study design: Other, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Parallel Assignment
Primary outcome: Effect of modafinil versus placebo on daytime sleepiness
Secondary outcome: Effect of modafinil versus placebo on cognitive performance
Detailed description:
A relatively new treatment for the excessive daytime sleepiness (EDS) associated with
inadequate sleep is the drug modafinil. Modafinil decreases subjective reports and objective
measures of daytime sleepiness under conditions of sleep restriction, while enhancing
cognitive performance. At the same time, sleep quality does not appear to be affected
significantly. Interestingly, recent clinical trials in cocaine-dependent populations
suggest that modafinil reduces the relapse to cocaine use, by unknown mechanisms.
We propose to employ both subjective and objective measures of nocturnal sleep and daytime
sleepiness, as well as measures of general cognitive performance and sleep-dependent memory
consolidation, to explore potential mechanistic relationships between cocaine abstinence,
EDS, and modafinil's efficacy in preventing cocaine relapse.
The following specific aims are proposed:
Specific Aim 1: To establish whether objective measures of poor nocturnal sleep (e. g.,
reduced total sleep time and sleep efficiency) that progressively characterize periods of
sustained cocaine abstinence are also associated with objective evidence of excessive daytime
sleepiness (EDS).
Specific Aim 2: To establish the ability of modafinil to reverse the excessive daytime
sleepiness (EDS) and deficits in cognitive performance that characterize cocaine abstinence.
Specific Aim 3: To conduct a pilot study to determine whether the observed abnormalities in
objective sleep, EDS, and/or cognitive function predict relapse to cocaine use and/or whether
successful abstinence from cocaine is associated with normalization of the same.
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Male or female individuals, ages 18-65, meeting current DSM-IV criteria for cocaine
dependence. Documented positive urine toxicology screen for cocaine at intake and
regular 3 times more weekly use of cocaine.
- Subject has voluntarily given informed consent and signed the informed consent
document(s).
- Able to read English and complete study evaluations.
Exclusion Criteria:
- Use of prescription medication in the past 6 months indicating a medical or
psychiatric condition that in the opinion of the PI would interfere with study
participation (e. g. hypertension, severe renal or hepatic disease, HIV, primary
psychotic disorder, primary mood disorder, primary sleep disorder).
- Meeting DSM-IV criteria for dependence on any substance other than cocaine and
nicotine.
- Significant underlying medical or psychiatric conditions or hypersensitivity to
modafinil that in the opinion of the PI would interfere with study participation.
- Abstinence from cocaine for more than one week prior to inpatient admission.
- Positive urine or serum pregnancy test.
- Women who are pregnant or lactating, or not using a reliable method of birth control.
- (For subjects completing the fMRI portion of the study) Presence of or history
indicative of ferromagnetic metal in their bodies.
Locations and Contacts
Peter Morgan, MD, PhD, Phone: 203-974-7515, Email: peter.morgan@yale.edu
Connecticut Mental Health Center, New Haven, Connecticut 06519, United States; Recruiting
Additional Information
Starting date: August 2006
Ending date: March 2010
Last updated: December 27, 2007
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