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Taking people in FranceNo phase

Tests brain stimulation to ease suicidal thoughts in depression

Tests brain stimulation with a mild current in adults with treatment-resistant depression.

Plain-language title generated from the registry record
Registry title: Effects of Transcranial Direct Current Stimulation (tDCS) in the Management of Suicidal Ideation

Key facts

Where
Faye-l'Abbesse and Poitiers, FranceSee the 2 sites

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with depression and suicidal thoughts who are taking a stable antidepressant. It tests brain stimulation with a weak electric current (tDCS).

Age
Over 18 years
Sex
All sexes can join.
Disease stage
A recurrent or single depressive episode (DSM IV criteria), with a MADRS score of 20 or more and an SSI score above 3.
Earlier treatment
Stable antidepressant treatment for 3 weeks.

Main reasons for not taking part

  • Depression with psychotic features, schizophrenia, or alcohol or other substance dependence or abuse
  • High suicide risk (MADRS item 10 above 4) without hospitalization
  • Already had electroconvulsive therapy for this episode and did not respond
  • Contraindication to tDCS, such as a metal implant in the brain or a pacemaker
  • Pregnant or breastfeeding women

Read by machine on 12 November 2026.

Where in France

  • Centre Hospitalier Nord-Deux-SèvresFaye-l'Abbesse, FranceContact: Issa WassoufTaking people
  • Centre Hospitalier Henri LaboritPoitiers, FranceContact: Ghina Harika-GermaneauTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Centre Hospitalier Henri Laborit
Trial code
NCT06009523
Record updated
23 October 2026
Original description
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 ideationRead full original descriptionShow less

Effects of Transcranial Direct Current Stimulation (tDCS) in the Management of Suicidal Ideation in Treatment-resistant Depression : a Pilot Study

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

Inclusion: 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 ≥ 20; SSI score > 3; Subject affiliated to a health insurance system; Woman with effective contraception and agreeing to maintain it throughout the study period.

Exclusion: Patient who has already undergone an electroconvulsive therapy course for the current episode and does not respond to this treatment; Contraindication to tDCS: intracerebral metallic implant (with the exception of dental implants), cardiac pacemaker, active or non-implanted devices in the region of the head, acute eczema in the planned stimulation area; Depression with psychotic features Axis I (DSM IV) co-morbid diagnosis of schizophrenia, alcohol and/or other substance dependence (or abuse) (lifetime); Patient deprived of liberty; Patient with high suicide risk (item 10 MADRS > 4) in the absence of hospitalization; Pregnant, parturient or breastfeeding woman; Simultaneous participation in another interventional research.

ClinicalTrials.gov NCT06009523