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tDCS & Auditory Hallucinations in Schizophrenia

H

Herzog Hospital

Status

Terminated

Conditions

Schizophrenia

Treatments

Device: Active tDCS
Device: control

Study type

Interventional

Funder types

Other

Identifiers

NCT02227563
Meiron 2013-3

Details and patient eligibility

About

The aim of this study is to evaluate tDCS effects on schizophrenia symptoms, particularly on auditory verbal hallucinations. tDCS applied with cathodal (inhibitory) electrode over the left temporal parietal junction and anodal (excitatory) electrode over the left dorsolateral prefrontal cortex.

Enrollment

3 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ages 18-60
  • Primary diagnosis of Diagnostic and Statistical Manual, fifth edition, schizophrenia
  • Persistent auditory verbal hallucinations
  • Right handed
  • Under stable doses of antipsychotic medication for ≥4 weeks
  • Normal hearing by self-report and physical exam
  • Use of effective method of birth control for women of childbearing capacity
  • Capable to provide informed consent. For patients judged to be incapable to provide informed consent the legal guardian of the patient must agree to participation in the study and provide signed informed consent

Exclusion criteria

  • Current or past history of substance dependence or abuse (excluding nicotine)
  • Other current Axis I disorders
  • History of seizure, epilepsy in self or first degree relatives, stoke, brain surgery, head injury, intracranial metal implants, known structural brain lesion, devices that may be affected by tDCS (pacemaker, medication pump, cochlear implant, implanted brain stimulator)
  • Frequent and persistent migraines
  • History of adverse reaction to neurostimulation
  • Participation in study of investigational medication within 6 weeks
  • Pregnancy
  • Women who are breast-feeding
  • Current significant laboratory abnormality

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

3 participants in 2 patient groups

Active tDCS
Experimental group
Description:
active tDCS
Treatment:
Device: Active tDCS
control
Sham Comparator group
Description:
sham (placebo) tDCS condition
Treatment:
Device: control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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