Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06009523

Effects of Transcranial Direct Current Stimulation (tDCS) in the Management of Suicidal Ideation

Led by Centre Hospitalier Henri Laborit · Updated on 2025-06-05

50

Participants Needed

2

Research Sites

213 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of this study is to demonstrate that 15 transcranial direct current stimulation (tDCS) sessions of 30 minutes at 2 mA intensity are effective to reduce suicidal ideation

CONDITIONS

Official Title

Effects of Transcranial Direct Current Stimulation (tDCS) in the Management of Suicidal Ideation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Written informed consent
  • Diagnosis of recurrent or isolated depressive episode according to DSM IV criteria (A.P.A. 1994)
  • Stable antidepressant treatment for 3 weeks
  • MADRS score 60 20
  • SSI score > 3
  • Affiliated to a health insurance system
  • Woman with effective contraception and agreeing to maintain it throughout the study period
Not Eligible

You will not qualify if you...

  • Depression with psychotic features Axis I (DSM IV) or co-morbid schizophrenia, alcohol and/or other substance dependence or abuse (lifetime)
  • Previous electroconvulsive therapy for current episode without response
  • Patient deprived of liberty
  • High suicide risk (MADRS item 10 > 4) without hospitalization
  • Contraindications to tDCS: intracerebral metallic implant (except dental implants), cardiac pacemaker, active or non-implanted devices in head region, acute eczema at stimulation site
  • Pregnant, parturient, or breastfeeding women
  • Participation in another interventional research

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Centre Hospitalier Nord-Deux-Sèvres

Faye-l'Abbesse, France

Actively Recruiting

2

Centre Hospitalier Henri Laborit

Poitiers, France

Actively Recruiting

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Research Team

G

Ghina Harika-Germaneau

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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