Bilateral Prefrontal Modulation in Alcoholism

N/ACompletedNCT02091284

Federal University of Espirito Santo49 enrolled

Overview

In this study, eligible alcoholic inpatients recruited from a specialized clinic for addiction treatment, filling inclusion criteria and not showing any exclusion criteria, were randomized to receive the repetitive (10 sessions, every other day) bilateral dorsolateral Prefrontal Cortex (dlPFC: cathodal left / anodal right) tDCS (2 milliamperes, 5 x 7 cm2, for 20 min) or placebo (sham-tDCS). Craving to the use of alcohol was examined before (baseline), during and after the end of the tDCS treatment. Based in our previous data, our hypothesis was that repetitive bilateral tDCS over dlPFC would favorably change craving in alcoholism and this would be a long-lasting effect.

Before (baseline) and after tDCS or sham-tDCS treatment, subjects were clinically examined regarding craving (obsessive compulsive drinking scale) and they were followed-up for relapses at least 3 months after treatment.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Drug Addiction Executive Dysfunction

Interventions

transcranial Direct Current StimulationDEVICE

Direct currents were transferred via a pair of carbonated-silicone electrodes (35 cm2) with a thick layer of high conductive gel for EEG underneath them. The electric current will be delivered by an electric stimulator. To stimulate the left DLPFC, the cathode electrode was placed over F3 according to the 10-20 international system while the anode was placed over the contralateral F4 region. The currents flowed continuously for 20 minutes with an intensity of 2 milliamperes.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * patients between the age of 18 and 60 years; * met criteria for alcohol dependence according to the Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV), as determined by clinical evaluation; * in stable clinical condition with no need for inpatient care; * able to read, write, and speak Portuguese; and * no severe withdrawal signs or symptoms at baseline. Exclusion Criteria: * a condition of intoxication or withdrawal due to a substance other alcohol; * unstable mental or medical disorder or substance abuse or addiction other than alcohol dependence, except nicotine and/or caffeine; * a diagnosis of epilepsy, convulsions, or delirium tremens during abstinence from alcohol; * a previous history of drug hypersensitivity or adverse reactions to diazepam or other benzodiazepines and haloperidol; * any contraindication for electrical brain stimulation procedures such as electronic implants or metal implants; * suspected pregnancy for female participants; * any contraindication for magnetic resonance procedures such as electronic implants, metal implants, claustrophobia, or permanent make-up or tattoo received within the previous 3 months; * the presence of vascular, traumatic, inflammatory, or tumor injuries detectable by CT examination.

Outcomes

Primary Outcomes

Craving

Five items from the original obsessive compulsive drinking scale, which are believed to reliably assess craving in a narrow sense were used. Questions of this brief scale allow quantification of thoughts and feelings (obsessions), and behavioral intentions, and are answered on a scale ranging from 0 to 4, resulting in a total score between 0 and 20. Higher scores reflect more severe craving. These items were applied at the beginning, during and at the end of the treatment with sham-tDCS or tDCS.

Time frame: Five applications: first week before tDCS treatment (baseline), second, third and fourth weeks, during the treatment, and in the fifth week, after the end of the tDCS treatment.