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

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.

Study Overview

• Status: Recruiting
• Conditions: Schizophrenia; Anodal Stimulation tDCS; Working Memory
• Intervention / Treatment: Procedure: Transcranial direct current stimulation

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).

• Study Type: Interventional
• Enrollment (Anticipated): 128
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Christian Plewnia, MD; Phone Number: ++49 (0)7071-2986121; Email: christian.plewnia@uni-tuebingen.de

Study Locations

• Germany
  • Muenchen, Germany
    • Recruiting
    • LMU Muenchen, Department of Psychiatry and Psychotherapy
    • Contact: Alkomiet Hasan, MD
  • Tuebingen, Germany, 72076
    • Recruiting
    • University Hospital Tuebigen, Department of Psychiatry and Psychotherapy
    • Contact: Christian Plewnia, MD; Phone Number: +49 7071 29 86121; Email: christian.plewnia@uni-tuebingen.de

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 60 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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 Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Transcranial direct current stimulation; tDCS with varying intensity, location and polarity	Procedure: Transcranial direct current stimulation; Other Names: tDCS
Placebo Comparator: Sham stimulation; Double blind sham stimulation with sham mode of neuroConn device	Procedure: Transcranial direct current stimulation; Other Names: tDCS

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of dprime	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	Assessment during stimulation in a n-back task at three specific timepoints during one week

Secondary Outcome Measures

Outcome Measure	Time Frame
Change of reaction time in n-back task	Assessment during stimulation in a n-back task at three specific timepoints during one week

Collaborators and Investigators

• Sponsor: University Hospital Tuebingen
• Collaborators: University Hospital Munich
• Investigators: Principal Investigator: Christian Plewnia, Prof., MD, University Hospital Tuebingen, Department of Psychiatry and Psychotherapy

Study record dates

Study Major Dates

• Study Start: October 1, 2015
• Primary Completion (Anticipated): August 1, 2022
• Study Completion (Anticipated): October 1, 2022

Study Registration Dates

• First Submitted: June 20, 2016
• First Submitted That Met QC Criteria: June 30, 2016
• First Posted (Estimate): July 6, 2016

Study Record Updates

• Last Update Posted (Actual): April 28, 2021
• Last Update Submitted That Met QC Criteria: April 27, 2021
• Last Verified: April 1, 2021

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Schizophrenia Spectrum and Other Psychotic Disorders; Schizophrenia
• Other Study ID Numbers: 01EE1407H

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No