Schizophrenia Clinical Trial
Official title:
Research on Transcranial Direct Current Stimulation (tDCS) as a Treatment for Cognitive Deficits in Schizophrenic
This trial attempts to evaluate the effects of intensive transcranial direct-current stimulation (tDCS) on improving cognition in schizophrenia patients and changes in resting state brain network connectivity, especially increasing connectivity in the tasks related network, and increasing activation the DLPFC in a working memory task. Half of the participants will be randomized to tDCS group, while the other half will be randomized to receive sham tDCS.
Schizophrenia patients (SZ) show profound and persistent cognitive deficits in attention,
executive processing, and verbal and visuospatial memory, which persist even after psychotic
symptoms are ameliorated. Cognitive deficits may be more important in preventing functional,
occupational, and social recovery in SZ than other symptom domains and are not effectively
treated by current pharmacological approaches. Transcranial direct-current stimulation (tDCS)
is less expensive than other modalities (e.g. repetitive transcranial magnetic stimulation;
rTMS), easily available, and has a good safety profile in healthy controls (HC) and SZ.
However, these prior studies did not make use of a validated measure such as the MATRICS
consensus battery (MCCB), which is now established as the standard for assessing cognitive
improvement in SZ. Despite these promising preliminary results, this effect of tDCS in SZ
needs to be confirmed and the underlying biological mechanism elucidated. Therefore, the
investigators employed MCCB to evaluate the effects on improving cognition and functional MRI
to explore the underlying mechanism.
Half of the participants will be randomized to tDCS group, while the other half will be
randomized to receive sham tDCS. Active vs. sham treatment will be randomly using computer
generated lists. Subjects and researcher-administrators of tDCS and testers or evaluators
will be blind to treatment.The main cognitive outcome measure, the MCCB, will be administered
at baseline and 1 day after the last tDCS session.Participants will be scanned once prior to
tDCS sessions, and within one day after the 10th tDCS sessions using our Siemens 3T Verio MRI
scanner.
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