Prefrontal Cortex Stimulation as Treatment for Crack-cocaine Addiction
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Purpose
The use of crack-cocaine is growing at alarming rate in our country and it is absolutely worrisome the fast establishment of addiction to it. Its immediate effects, that are intense and extremely fleeting, increase dramatically the probability of this drug to be consumed again, settling quickly down the loss of control and the compulsive use, turning the effects of this drug highly addictive. Parallel to this process, brain damages are quickly established, progressing to severe impairments of frontal functions, leading to the lack of cognitive control that feeds back and aggravates the dependence, and hampers any therapeutic approach. The existing treatments have not proved to be satisfactory yet. Thus, considering that a new modality of treatment, based on the neuromodulation induced by noninvasive brain stimulation, has been useful in treating various neuropsychiatric conditions, this study will examine the potential beneficial effects of repeated transcranial Direct Current Stimulation over the left dorsolateral prefrontal cortex in the treatment of crack-cocaine addiction.
| Condition | Intervention | Phase |
|---|---|---|
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Cocaine Addiction Cocaine-related Disorder Executive Dysfunction |
Device: transcranial Direct Current Stimulation |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator) Primary Purpose: Treatment |
| Official Title: | Treatment of Crack-cocaine Addiction Through Cognitive Neuromodulation of the Prefrontal Cortex Produced by Transcranial Direct Current Stimulation. |
- changes in the relapse frequencies to the use of crack-cocaine [ Time Frame: after two-weeks treatment with active-tDCS or sham-tDCS ] [ Designated as safety issue: No ]changes in the number of relapses to the use of crack-cocaine after the completion of two-weeks of treatment sessions with active-tDCS or sham-tDCS.
- Intensity of the urge to the use of crack-cocaine [ Time Frame: before and after ERP in two weekly sessions over two weeks ] [ Designated as safety issue: No ]The intensity of craving will be examined by a short scale, the Brief Cocaine Craving Questionnaire developed by Sussner et al (2006)
- Event Related Potentials [ Time Frame: twice a week over two consecutive weeks during the treatment ] [ Designated as safety issue: No ]Event Related Potentials (ERPs) elicited by random presentation of three related images and three non-related images to crack use every Monday and Friday over the two-weeks period of active-tDCS or sham-tDCS.
- Cognitive tests [ Time Frame: Before the first experimental session, in the middle of the protocol and two days after the last experimental session ] [ Designated as safety issue: No ]Cognitive tests are comprised by frontal assessment battery (FAB), Mini-Mental Status Examination (MMSE), verbal n-back task, visuospatial n-back task, go/no-go test, couting Stroop test.
- State of depression [ Time Frame: Before the first experimental session, in the middle of the treatment and after the last experimental session. ] [ Designated as safety issue: No ]It will be applied Hamilton Scale for Depression, a structured multiple choice questionnaire used to assess the severity of the symptoms of depression. It will be applied with cognitive tests.
| Estimated Enrollment: | 40 |
| Study Start Date: | June 2011 |
| Estimated Study Completion Date: | May 2013 |
| Estimated Primary Completion Date: | November 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Sham Comparator: sham-tDCS
the electrodes are positioned in the same manner as the active-tDCS, activated for 20 s (time to climb ramp of the current until reach the current intensity used in the experiment), enough to produce the sensation of itch, and turned off until the end of the session.
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Device: transcranial Direct Current Stimulation
transcranial Direct Current Stimulation (tDCS) will be applied by electrodes (5 x 7 cm2), with intensity of 2 mA, during 20 min, with cathode over the left dorsolateral prefrontal cortex (F3 site) and anode placed in the contralateral dorsolateral prefrontal cortex (F4 site).
Other Names:
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Experimental: active-tDCS
low-intensity transcranial Direct Current Stimulation (tDCS)applied over the dorsolateral prefrontal cortex
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Device: transcranial Direct Current Stimulation
transcranial Direct Current Stimulation (tDCS) will be applied by electrodes (5 x 7 cm2), with intensity of 2 mA, during 20 min, with cathode over the left dorsolateral prefrontal cortex (F3 site) and anode placed in the contralateral dorsolateral prefrontal cortex (F4 site).
Other Names:
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Detailed Description:
Forty subjects between 18 and 60 years old, both genders, with a diagnosis of dependence on crack-cocaine, evaluated for the first time at the Center for Psychosocial Care for Alcohol and Other Drugs (CAPS-AD, in Portuguese) in the municipality of Serra, ES, Brazil, will be invited to participate in this study. After triage, following the inclusion and exclusion criteria, they will be informed in details about the experimental protocol and, if they agree to participate, it will be required to sign an Informed Consent. It Will be applied a structured anamnesis, made a psychiatric clinical and physical examination. The treatment will be started with regular medications for abstinence and comorbidities and psychosocial approaches usually done in the CAPS-AD. After selected they will be referred to the Laboratory of Cognitive Science and Neuropsychopharmacology of the Postgraduate Program in Physiological Sciences from Health Sciences Center of Federal University of Espírito Santo where they will be semi-randomly (matched for age, gender and sociodemographic characteristics) distributed into two different groups: (A) sham-tDCS (n = 20) and (B) active-tDCS (n = 20); and they will follow for 10 applications in daily sessions, excepting on weekends, of transcranial direct current stimulation (tDCS, 5 x 7 cm2, 2 mA, 20 min) over the left dorsolateral prefrontal cortex or sham procedure. Event-related potentials (ERP) will be recorded before, during and after brain stimulation or sham procedure under random presentation of three related images and three non-related images to crack use. The compulsive behavior will be evaluated before and after the ERP records. Cognitive tests which assess mental function, frontal function, visuospatial and verbal working memory, inhibition, and conflict resolution will be performed. The depression will be assessed during the treatment, and the addicted subjects will be evaluated once a week for four consecutive weeks after a series of applications of sham-tDCS or active-tDCS.
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- fulfill the criteria for the crack-dependence syndrome, based on criteria of the International Classification of Diseases on its 10th version;
- all users and addicts who make use of crack-cocaine alone or in combination with other drugs (alcohol, nicotine, caffeine, cannabis, etc.), or who have psychiatric comorbidities (anxiety, depression, etc.)
- must be clinically stable and not requiring hospitalization;
- should be clinically suitable for the treatment proposed in this study;
- need to be able to read, write and speak Portuguese
Exclusion Criteria:
- should not present current or past illnesses that may be aggravated during treatment;
- may not show abnormalities in laboratory tests which suggest a deterioration of its physical condition for participation in the study;
- individuals who have some metal in the brain or skull (chips, fragments, pins, etc. - except titanium);
- history of epilepsy, severe brain trauma, cochlear implant, cardiac pacemaker or intracardiac metal apparatus);
- pregnants.
Contacts and Locations| Contact: Ester M Nakamura-Palacios, MD, PhD | +55 27 3335-7337 | emnpalacios@gmail.com |
| Contact: Roney WD Oliveira, MD, PhD | +55 27 3335-7337 | rwddo@uol.com.br |
| Brazil | |
| Laboratory of Cognitive Sciences and Neuropsychopharmacology, Post-Graduation Program in Physiologycal Sciences, Health Sciences Center, Federal University of Espírito Santo | Recruiting |
| Vitória, Espírito Santo, Brazil, 29042-755 | |
| Contact: Ester M Nakamura-Palacios, MD, PhD +55 27 3335-7337 emnpalacios@gmail.com | |
| Contact: Roney WD Oliveira, MD, PhD +55 27 3335-7337 rwddo@uol.com.br | |
| Principal Investigator: Ester M Nakamura-Palacios, MD, PhD | |
| Principal Investigator: | Ester M Nakamura-Palacios, MD, PhD | Federal University of Espírito Santo |
More Information
Publications:
| Responsible Party: | Ester Miyuki Nakamura-Palacios, MD, PhD, Federal University of Espirito Santo |
| ClinicalTrials.gov Identifier: | NCT01337297 History of Changes |
| Other Study ID Numbers: | CEP-UFES 296/10 |
| Study First Received: | April 14, 2011 |
| Last Updated: | December 10, 2011 |
| Health Authority: | Brazil: Ethics Committee |
Keywords provided by Federal University of Espirito Santo:
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crack cocaine addiction tDCS ERP |
P300 attention inhibitory control working memory |
Additional relevant MeSH terms:
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Cocaine-Related Disorders Behavior, Addictive Compulsive Behavior Impulsive Behavior Substance-Related Disorders Mental Disorders Cocaine Vasoconstrictor Agents Cardiovascular Agents Therapeutic Uses Pharmacologic Actions Dopamine Uptake Inhibitors |
Dopamine Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Neurotransmitter Uptake Inhibitors Physiological Effects of Drugs Anesthetics, Local Anesthetics Central Nervous System Depressants Sensory System Agents Peripheral Nervous System Agents Central Nervous System Agents |
ClinicalTrials.gov processed this record on May 23, 2013