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?Effect of transcranial direct current stimulation on drug craving of addicts

Assessment of the effect of transcranial direct current stimulation on drug cue-induced craving in abstinent methamphetamine users using a visual paradigm and its prediction using resting state EEG signals

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170808035562N2
Enrollment
60
Registered
2018-06-16
Start date
2018-06-22
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

Methamphetamine dependence disorder. Opioid dependence

Interventions

Intervention 1: Intervention group: Direct current will be delivered using a StarStimtCS system and transferred by a pair of circular stimulation electrodes with 1 cm radius. They have rear-fill apert

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 61 Years

Inclusion criteria

Inclusion criteria: Male gender Age =18 and <61 years old Farsi speaking Diagnosed with Methamphetamine Use Disorder (last 12 months) based on Structured Clinical Interview for DSM-5 (SCID-5) Abstinent from any drugs except cigarettes for at least one week based on medical records or self-report, confirmed by urine analysis Positive response to Methamphetamine cue-reactivity screening (MCS) Willing and capable of interacting with the informed consent process8. The ability to understand, read and answer the tests

Exclusion criteria

Exclusion criteria: Unwillingness or inability to complete any of the major aspects of the study protocol, including drug cue rating, or behavioral assessment. Abstinence from methamphetamine for more than 6 months based on self-report Any major clinical psychiatric disorder, assessed by Structured Clinical Interview for DSM-5 (SCID-5) Active suicidal ideation with intent or plan determined by self-report or assessment by PI or study staff during the initial screening or any other phase of the study Positive drug test for amphetamines, opioids, cannabis confirmed by urine tests Any active skin disorder that affects skin integrity of the scalp Having any condition that would preclude undergoing a tDCS stimulation based on the tDCS safety checklist Unstable medical disorder reported in subject’s medical history or by a clinician assessment History of major head trauma, seizure, brain surgery, intracranial metal implantation Non-correctable vision or hearing problems.

Design outcomes

Primary

MeasureTime frame
Amplitude of event-related potentials with middle latency (P3). Timepoint: Immediately before and after intervention. Method of measurement: Event-related potentials will be recorded using a bio-signal amplifier with CE & FDA approval (g.HIamp, g.tec company ) from 62 scalp sites.;Amplitude of event-related potentials with late latency (LPP). Timepoint: Immediately before and after intervention. Method of measurement: Event-related potentials will be recorded using a bio-signal amplifier with CE & FDA approval (g.HIamp, g.tec company ) from 62 scalp sites.;Amplitude of event-related potentials with early latency (<300 ms). Timepoint: Immediately before and after intervention. Method of measurement: Event-related potentials will be recorded using a bio-signal amplifier with CE & FDA approval (g.HIamp, g.tec company ) from 62 scalp sites.

Secondary

MeasureTime frame
Functional brain connectivity. Timepoint: Before intervention-after intervention. Method of measurement: Weighted Phase Lag Index.;Effective brain connectivity. Timepoint: Before intervention-after intervention. Method of measurement: Granger causality method.;?electric neuronal activities. Timepoint: Before intervention-after intervention. Method of measurement: Source reconstruction methods such as Standardized low-resolution brain electromagnetic tomography (sLORETA).;Craving for Methamphetamin. Timepoint: Before, during & after. Method of measurement: Visual Analogue Scale (VAS).;Craving for Methamphetamine. Timepoint: Before & after. Method of measurement: Desire for Drug Questionnaire.;Depression. Timepoint: After intervention. Method of measurement: Depression Anxiety and Stress Scale (DASS).;Impulsivity. Timepoint: After Intervention. Method of measurement: Barratt Impulsiveness Scale.;Positive & Negative Affect. Timepoint: Before and After Intervention. Method of measurement: Positive and Negative Affect Scale.;Anxiety. Timepoint: After Intervention. Method of measurement: Depression Anxiety and Stress Scale (DASS).;Stress. Timepoint: ????? ????????????. Method of measurement: Depression Anxiety and Stress Scale (DASS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Khajehpour

Tehran University of Medical Sciences

h-khajehpoor@razi.tums.ac.ir+98 21 6695 3144

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026