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Interest of tDCS in Help for Supporting Alcohol Abstinence

NCT03287154, Not applicable, Completed, Centre Hospitalier Henri Laborit

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleInterest of tDCS in Help for Supporting Alcohol AbstinenceClinicalTrials.gov
NCT numberNCT03287154ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment90 participants, actualClinicalTrials.gov
Lead sponsorCentre Hospitalier Henri LaboritClinicalTrials.gov
ConditionsAlcoholic IntoxicationClinicalTrials.gov
InterventionsActive tDCS stimulations, Sham tDCSClinicalTrials.gov
First posted2017-09-19ClinicalTrials.gov
Last updated2026-01-13ClinicalTrials.gov

Registered outcomes 12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryAlcohol Abstinence3 monthsThe primary outcome is to evaluate the interest of the transcranial Direct Current Stimulation (tDCS) for helping the abstinence support in addictive alcoholic patients.ClinicalTrials.gov
SecondaryRelapse control6 monthsEvaluation of tDCS interest in help for relapse control.ClinicalTrials.gov
SecondaryAlcohol consumption6 monthsImpact on alcohol consumption based on the Total Alcohol Consumption (TAC).ClinicalTrials.gov
SecondaryAnxiety-depression6 monthsImpact on the anxiety-depression symptomatologyClinicalTrials.gov
SecondaryTobacco consumption6 monthsImpact on tobacco consumption (decrease of cigarette consumption).ClinicalTrials.gov
SecondarySafety assessment with adverse and/or intercurrent events analysis.6 months
The clinical tolerability will be objectified through the analysis of adverse and /or intercurrent events occuring all along the study. Theses events will be assessed at every study visit during patient examination.
ClinicalTrials.gov
SecondaryCognitive functions assessments with the Moca-test questionnaire.6 monthsThe score to the Moca-test will permit to assessed the cognitive functions from baseline (week 0) to the week 14 and from baseline from the week 26.ClinicalTrials.gov
SecondaryExecutive functions assessments with the scale Barratt Impulsiveness Scale (BIS 11).6 monthsThis examination will be assessed from week 0 to Day 9, from week 0 to week 14 and from week 0 to week 26.ClinicalTrials.gov
SecondaryExecutive functions assessments with the Go NoGo task.6 monthsThis examination will be assessed from week 0 to Day 9, from week 0 to week 14 and from week 0 to week 26.ClinicalTrials.gov
SecondaryExecutive functions assessments with the Wisconsin Card Sorting Test (WCST).6 monthsThis examination will be assessed from week 0 to Day 9, from week 0 to week 14 and from week 0 to week 26.ClinicalTrials.gov
SecondaryExecutive functions assessments with the Stroop test.6 monthsThis examination will be assessed from week 0 to Day 9, from week 0 to week 14 and from week 0 to week 26.ClinicalTrials.gov
SecondaryExecutive functions assessments with the IOWA Gambling Task (IGT).6 monthsThis examination will be assessed from week 0 to Day 9, from week 0 to week 14 and from week 0 to week 26.ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 4

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Card Sorting Test (Berg)Secondary outcomeConductCognition
Go/No-Go TaskSecondary outcomeConductCognition
Iowa Gambling LiteSecondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)