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Efficacy of tDCS in the Treatment of Resistant Auditory Hallucinations in Schizophrenia (TDCSHALLU)

C

Centre hospitalier de Ville-Evrard, France

Status

Enrolling

Conditions

Refractory Schizophrenia
Schizophrenia
Hallucinations

Treatments

Device: transcranial direct current stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04352569
DMDPT-TCH/MM/2015-A00842-47

Details and patient eligibility

About

The regions which are assumed to underlie the pathophysiology of schizophrenia, namely hypoactivity at the prefrontal level and pathological hyperactivity of the associative regions of the language located in the left temporoparietal region.

To assess the efficacy of tDCS on auditory hallucinations, the investigators performs an randomized double blind versus placebo trial. In each arms patients will receive two tDCS sessions a day during two weeks.

Full description

Hearing hallucinations are one of the major symptoms of schizophrenia. In 30% of patients they are resistant to common psychotropic treatments. tDCS (Transcranial Direct Current Stimulation) is a technical of brain stimulation, non-invasive, painless that modulates brain activity by the transcranial administration of a low-intensity electric current, via two electrodes (an anode and a cathode). Several scientifics studies have reported a beneficial effect of tDCS in the treatment of pain, depression and especially hearing hallucinations in schizophrenia.

The main study purpose is to evaluate the effectiveness of tDCS on resistant auditory hallucinations in patients with schizophrenia.

Then, to evaluate the effectiveness of tDCS on global schizophrenic symptomatology and to assess the impact of tDCS on patients' quality of life.

Also the study, evaluate the impact of tDCS on cortical excitability. We measure the change in serum BDNF (Brain Derived Neutrophic Factor) before and after tDCS stimulation. Indeed, to evaluate the impact of tDCS on neurocognitive functions.

Patients will receive either active tDCS or placebo tDCS randomly. All patients will have two tDCS/day sessions, one hour apart, for 2 working weeks. The stimulation parameters will be consistent with the literature data, namely: Intensity = 2mA; duration of sessions = 20 minutes; total number of sessions = 20 (2 daily sessions for two working weeks).

Enrollment

44 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Schizophrenia according to DSM-V.
  • Refractory auditory hallucinations(despite two antipsychotics trials).
  • Right-handed patients.
  • Written informed consent.

Exclusion criteria

  • Presence of other psychiatric disorders than schizophrenia (except addiction to tobacco or caffeine ).
  • History of severe head trauma or coma.
  • History of epilepsy or neurological disorder or a general medical condition.
  • Presence of intracranial metallic objects or pacemaker.
  • Hospitalized patients without consent.
  • pregnant women .

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

44 participants in 2 patient groups

transcranial direct current stimulation
Active Comparator group
Description:
The transcranial direct current stimulation (tDCS) with two elecrodes placed over the scalp: the anode over the LTP, le cathode over L DLPFG.
Treatment:
Device: transcranial direct current stimulation
transcranial direct current stimulation sham
Sham Comparator group
Description:
tDCS device allows sham stimulation. This technic give the same impression that active stimulation and allows optimum placebo stimulation.
Treatment:
Device: transcranial direct current stimulation

Trial contacts and locations

1

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Central trial contact

Rusheenthira THAVASEELAN, Msc; NOOMANE BOUAZIZ, MD

Data sourced from clinicaltrials.gov

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