Schizophrenia Clinical Trial
Official title:
Transcranial Alternating Current Stimulation (tACS) for Cognitive Impairments in Patients With Schizophrenia: a Randomized Controlled Trial
This trial attempts to investigate whether 10 sessions of tACS improves cognitive function, especially which domains of cognitive function are most improved and to investigate whether 10 sessions of tACS affecting brain activation during a working memory task and changes patterns of brain connectivity networks.Subjects will be divided into 2 groups 2:1, active and sham tACS. 50 subjects will be in the active group, and 25 subjects in the sham group (specific numbers to be decided on later).
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. Alternating current stimulation (tACS) 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. The ability
to entrain γ oscillations with 40Hz tACS, might compensate more specifically for this deficit
in γ oscillations in schizophrenia, and, may therefore, produce more robust behavioral
improvements in working memory and other aspects of cognition.However, no studies have looked
at the effects of multiple daily tACS stimulation at a 40HZ γ frequency on cognitive function
and symptoms in schizophrenia. This provides a rationale for the current study, which
proposes to investigate the effects of 10 sessions of 40HZ tACS on cognitive functions,
symptoms in schizophrenia.
Active vs. sham treatment will be randomly assigned in a 2:1 fashion (A:S) in groups using
computer generated lists. Subjects and tDCS testers or evaluators will be blind to treatment.
Subjects will be evaluated with cognitive, symptom and functional measures at baseline,
within 1 day ( or 2 days fro some measures) after 10 sessions, 2 weeks after 10 sessions, 1
month after 10 sessions, and 2 months after 10 sessions.After the 1 month evaluation,
subjects in the initial active tACS group will be randomly assigned to receive either 5
booster sessions of either active or sham tACS ( 25 subjects each), following parameters used
in the initial treatment. Subjects in the initial Sham group will receive 5 booster session
Sham tACS. Participants will be scanned once prior to tACS sessions, and within 3 days after
the 10th tACS session, using our Siemens 3T Tim Verio MRI scanner with a standard 32-channel
phased-array head coil.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05039489 -
A Study on the Brain Mechanism of cTBS in Improving Medication-resistant Auditory Hallucinations in Schizophrenia
|
N/A | |
Completed |
NCT05111548 -
Brain Stimulation and Cognitive Training - Efficacy
|
N/A | |
Completed |
NCT05321602 -
Study to Evaluate the PK Profiles of LY03010 in Patients With Schizophrenia or Schizoaffective Disorder
|
Phase 1 | |
Completed |
NCT04503954 -
Efficacy of Chronic Disease Self-management Program in People With Schizophrenia
|
N/A | |
Completed |
NCT02831231 -
Pilot Study Comparing Effects of Xanomeline Alone to Xanomeline Plus Trospium
|
Phase 1 | |
Completed |
NCT05517460 -
The Efficacy of Auricular Acupressure on Improving Constipation Among Residents in Community Rehabilitation Center
|
N/A | |
Completed |
NCT03652974 -
Disturbance of Plasma Cytokine Parameters in Clozapine-Resistant Treatment-Refractory Schizophrenia (CTRS) and Their Association With Combination Therapy
|
Phase 4 | |
Recruiting |
NCT04012684 -
rTMS on Mismatch Negativity of Schizophrenia
|
N/A | |
Recruiting |
NCT04481217 -
Cognitive Factors Mediating the Relationship Between Childhood Trauma and Auditory Hallucinations in Schizophrenia
|
N/A | |
Completed |
NCT00212784 -
Efficacy and Safety of Asenapine Using an Active Control in Subjects With Schizophrenia or Schizoaffective Disorder (25517)(P05935)
|
Phase 3 | |
Completed |
NCT04092686 -
A Clinical Trial That Will Study the Efficacy and Safety of an Investigational Drug in Acutely Psychotic People With Schizophrenia
|
Phase 3 | |
Completed |
NCT01914393 -
Pediatric Open-Label Extension Study
|
Phase 3 | |
Recruiting |
NCT03790345 -
Vitamin B6 and B12 in the Treatment of Movement Disorders Induced by Antipsychotics
|
Phase 2/Phase 3 | |
Recruiting |
NCT05956327 -
Insight Into Hippocampal Neuroplasticity in Schizophrenia by Investigating Molecular Pathways During Physical Training
|
N/A | |
Terminated |
NCT03209778 -
Involuntary Memories Investigation in Schizophrenia
|
N/A | |
Terminated |
NCT03261817 -
A Controlled Study With Remote Web-based Adapted Physical Activity (e-APA) in Psychotic Disorders
|
N/A | |
Completed |
NCT02905604 -
Magnetic Stimulation of the Brain in Schizophrenia or Depression
|
N/A | |
Recruiting |
NCT05542212 -
Intra-cortical Inhibition and Cognitive Deficits in Schizophrenia
|
N/A | |
Completed |
NCT04411979 -
Effects of 12 Weeks Walking on Cognitive Function in Schizophrenia
|
N/A | |
Terminated |
NCT03220438 -
TMS Enhancement of Visual Plasticity in Schizophrenia
|
N/A |