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

NCT ID: NCT02823639

Last Updated: 2021-04-28

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 128 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2022-10-31

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).

Conditions

Anodal Stimulation tDCS; Schizophrenia; Working Memory

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Transcranial direct current stimulation

tDCS with varying intensity, location and polarity

Group Type: ACTIVE_COMPARATOR

Transcranial direct current stimulation

Intervention Type: PROCEDURE

Sham stimulation

Double blind sham stimulation with sham mode of neuroConn device

Group Type: PLACEBO_COMPARATOR

Transcranial direct current stimulation

Intervention Type: PROCEDURE

Interventions

Transcranial direct current stimulation

Intervention Type: PROCEDURE

Other Intervention Names

tDCS

Eligibility Criteria

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)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital Munich

OTHER

Sponsor Role: collaborator

University Hospital Tuebingen

OTHER

Sponsor Role: lead

Responsible Party

Christian Plewnia, MD

Prof. Dr.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Christian Plewnia, Prof., MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Tuebingen, Department of Psychiatry and Psychotherapy

Locations

LMU Muenchen, Department of Psychiatry and Psychotherapy

München, , Germany

Site Status: RECRUITING

University Hospital Tuebigen, Department of Psychiatry and Psychotherapy

Tübingen, , Germany

Site Status: RECRUITING

Countries

Germany

Central Contacts

Christian Plewnia, MD

Role: CONTACT

christian.plewnia@uni-tuebingen.de

++49 (0)7071-2986121

Facility Contacts

Alkomiet Hasan, MD

Role: primary

Christian Plewnia, MD

Role: primary

christian.plewnia@uni-tuebingen.de

+49 7071 29 86121

Other Identifiers

01EE1407H

Identifier Type: -

Identifier Source: org_study_id