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Efficacy of dTMS in alcohol dependence

Not Applicable
Conditions
Health Condition 1: F102- Alcohol dependenceHealth Condition 2: F102- Alcohol dependence
Registration Number
CTRI/2023/04/051305
Lead Sponsor
Central Institute of Psychiatry
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients diagnosed with mental and behavioural disorders due to use of alcohol, dependence syndrome, currently using the substance (F10.24) as per International Classification of disease 10th (ICD-10, DCR)Diagnostic criteria for research.

2. Male gender

3. Age between 18-50 years

4. Ready to give written informed consent

5. Clinical institute withdrawal assessment for alcohol revised (CIWA-ar) score less than 10.

Exclusion Criteria

1. Any other co-morbid substance dependence except nicotine and caffeine.

2. Participants with any co-morbid psychiatric disorder.

3. History of severe withdrawal e.g., convulsions or delirium tremens during abstinence.

4. Color-blind patients

5. Not willing to give written informed consent.

6. Patient with presence of pacemaker or other electronic implants, metal or magnetic objects in the brain.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in scores of craving as rated by Alcohol Craving Questionnaire (ACQ) and Obsessive Compulsive Drinking Scale (OCDS).Timepoint: Reduction in scores of craving as rated by Alcohol Craving Questionnaire (ACQ) and Obsessive Compulsive Drinking Scale (OCDS) as assessed at the <br/ ><br>end of 2 weeks <br/ ><br>of dTMS treatment and after 4 weeks.
Secondary Outcome Measures
NameTimeMethod
Changes in the amplitude and latency of the P300 component of ERP on Stroop task.Timepoint: Changes in the amplitude and latency of the P300 component of ERP on Stroop task will be assessed before and at end of 2 weeks of dTMS treatment
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