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Efficacy and Mechanisms of Transcranial Direct Current Stimulation (tDCS) - Effects on Working Memory in Schizophrenia

Not Applicable
Conditions
Schizophrenia
Working Memory
Anodal Stimulation tDCS
Interventions
Procedure: Transcranial direct current stimulation
Registration Number
NCT02823639
Lead Sponsor
University Hospital Tuebingen
Brief Summary

Impairments of cognition are a core, severely disabling feature of schizophrenia leading to poor long-term outcome with no established treatment available.

Particularly impaired executive functions (e.g working memory) are frequently observed and are consistently associated with reduced activation of the dorsolateral prefrontal cortex (dlPFC). Deficits in those functions have been shown to be closely related to negative symptoms, thought disorder, and functional outcome in schizophrenia leading to the notion that frontal lobe dysfunction is crucially important in schizophrenic psychopathology.

Noninvasive brain stimulation like tDCS can enhance executive functions like working memory in healthy subjects as well as in patients. To identify the optimal parameters for this intervention in patients with schizophrenia, the investigators first test the effects of different polarities (anodal, cathodal), stimulation intensities (1mA, 2mA) and laterality (left, right) on working-memory performance (nback task) in a sham-controlled cross-over design (n=128). To elucidate mechanisms of action, oscillatory brain activity will be registered with electroencephalography (EEG).

These experiments will provide reliable data for an evidence-based development of new clinical interventions to improve treatment of cognitive deficits in patients with schizophrenia and thus enhance schizophrenia prevention and recovery.

Detailed Description

1. Working hypothesis:

In patients with subacute schizophrenia, transcranial direct current stimulation (tDCS) to the dorsolateral prefrontal cortex (dlPFC) exerts lasting beneficial effects on working-memory performance.

2. Research question(s):

In patients with remitted early phase schizophrenia, this research project aims at providing evidence for:

i) immediate improvement of working-memory performance by application of tDCS to the dlPFC in patients with schizophrenia; ii) determination of the optimal stimulation polarity, dosage and localization; iii) neurophysiological mechanisms (modulation in oscillatory activity and functional connectivity) and predictors of tDCS effects; iv) modulating effect of gender on the malleability of executive functions with tDCS.

3. Previous work of the investigators:

The investigators have provided proof-of principle evidence for persisting improvement of cognitive planning by a polarity-specific learning-stage dependent coupling of training and stimulation. The investigators have demonstrated that working memory and deficient cognitive control can be enhanced with anodal tDCS in depression and that the effects of tDCS are modulated by genetic polymorphisms. The investigators were the first to show impaired cortical plasticity following tDCS in schizophrenia patients at different disease states. Finally, the investigators have just successfully finished the world-wide largest clinical trial investigating the efficacy of non-invasive brain stimulation (rTMS) on negative symptoms in schizophrenia (DFG 241/10-1, Falkai, Hasan).

4. Aims and work plan:

To examine the potential of tDCS for the improvement of working memory with remitted schizophrenia the investigators are following this work plan:

I) Immediate effects on performance:

Assessment of efficacy of tDCS polarity (anodal, cathodal), dosage (1mA, 2mA) and laterality (left and right dlPFC) on working memory (adaptive n-back(6)) in patients (n=2x2x2x16=128). In a two-session cross-over design, stimulation (tDCS and sham) will be applied to the dlPFC (left or right) for 20min (during task performance).

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
128
Inclusion Criteria
  • diagnosed schizophrenia (DSM-V)
  • age (18 - 60 years)
  • right handedness
  • stable medication during 1 week of treatment and 1 week before
Exclusion Criteria
  • history of seizures
  • metal device throughout the body
  • pregnancy
  • use of anticonvulsive medication
  • use of benzodiazepines more than 1 mg of Lorazepam equivalent
  • current substance abuse (nicotine excluded)

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Transcranial direct current stimulationTranscranial direct current stimulationtDCS with varying intensity, location and polarity
Sham stimulationTranscranial direct current stimulationDouble blind sham stimulation with sham mode of neuroConn device
Primary Outcome Measures
NameTimeMethod
Change of dprimeAssessment during stimulation in a n-back task at three specific timepoints during one week

dprime provides the separation between the means of the signal and the noise distributions, compared against the standard deviation of the signal plus noise distributions

Secondary Outcome Measures
NameTimeMethod
Change of reaction time in n-back taskAssessment during stimulation in a n-back task at three specific timepoints during one week

Trial Locations

Locations (2)

University Hospital Tuebigen, Department of Psychiatry and Psychotherapy

🇩🇪

Tuebingen, Germany

LMU Muenchen, Department of Psychiatry and Psychotherapy

🇩🇪

Muenchen, Germany

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