TMS Enhancement of Visual Plasticity in Schizophrenia
Status: | Recruiting |
---|---|
Conditions: | Schizophrenia |
Therapuetic Areas: | Psychiatry / Psychology |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 2/7/2019 |
Start Date: | September 27, 2017 |
End Date: | December 25, 2019 |
Contact: | Jessica Sewell |
Email: | jsewell@som.umaryland.edu |
Phone: | 410-402-6801 |
Testing TMS Enhancement of Visual Plasticity in Schizophrenia
The major goal is to determine if Transcranial magnetic stimulation (TMS) enhances visual
plasticity in schizophrenia. TMS sessions (sham/placebo and real TMS) will be conducted
before two MRI scans with two weeks in-between to assess whether TMS stimulation to the
visual cortex will enhance visual plasticity in patients with schizophrenia-spectrum
disorders. This project may provide a better understanding of the underlying neurobiological
mechanisms responsible for learning and memory deficits in schizophrenia.
plasticity in schizophrenia. TMS sessions (sham/placebo and real TMS) will be conducted
before two MRI scans with two weeks in-between to assess whether TMS stimulation to the
visual cortex will enhance visual plasticity in patients with schizophrenia-spectrum
disorders. This project may provide a better understanding of the underlying neurobiological
mechanisms responsible for learning and memory deficits in schizophrenia.
Learning and memory impairments are commonly observed in schizophrenia spectrum disorders.
Alterations in "long-term potentiation" (LTP), a basic mechanism underlying learning and
memory, may explain this impairment. This project will assess fMRI visual plasticity, thought
to reflect LTP, in participants with and without schizophrenia spectrum disorders. Previous
studies have shown that visual plasticity is impaired in schizophrenia. The major goal is to
determine if Transcranial magnetic stimulation (TMS) enhances visual plasticity in
schizophrenia. Transcranial magnetic stimulation (TMS) provides a non-invasive means for
altering brain electrical neural activity. TMS sessions (sham/placebo and real TMS) will be
conducted before two MRI scans with two weeks in-between to assess whether TMS stimulation to
the visual cortex will enhance visual plasticity in patients with schizophrenia-spectrum
disorders. This project may provide a better understanding of the underlying neurobiological
mechanisms responsible for learning and memory deficits in schizophrenia.
Alterations in "long-term potentiation" (LTP), a basic mechanism underlying learning and
memory, may explain this impairment. This project will assess fMRI visual plasticity, thought
to reflect LTP, in participants with and without schizophrenia spectrum disorders. Previous
studies have shown that visual plasticity is impaired in schizophrenia. The major goal is to
determine if Transcranial magnetic stimulation (TMS) enhances visual plasticity in
schizophrenia. Transcranial magnetic stimulation (TMS) provides a non-invasive means for
altering brain electrical neural activity. TMS sessions (sham/placebo and real TMS) will be
conducted before two MRI scans with two weeks in-between to assess whether TMS stimulation to
the visual cortex will enhance visual plasticity in patients with schizophrenia-spectrum
disorders. This project may provide a better understanding of the underlying neurobiological
mechanisms responsible for learning and memory deficits in schizophrenia.
Inclusion Criteria:
1. age: 18-65,
2. no neurological illness, head trauma, or major medical illness,
3. not pregnant or nursing,
4. no contraindication for TMS or MRI scanning,
5. no current substance abuse/dependence.
Healthy controls will have no DSM-5 diagnosis and no first-degree relatives with a
psychotic disorder.
Inclusion criteria for patients includes:
1. DSM-5 diagnosis of schizophreniform, schizophrenia or schizoaffective and competent to
sign an informed consent,
2. not currently taking other medications that affects brain structure (e.g. steroids),
3. less than 12 months antipsychotic exposure and on the same psychotropic medications
for 4 weeks prior to study,
4. not be taking clozapine (due to its effects on NMDA receptors and increase of seizure
threshold),
5. clinically stable (i.e. no change in psychotic symptoms for at least 4 weeks).
Exclusion Criteria:
1. age outside of 18-65,
2. neurological illness, head trauma, or major medical illness,
3. pregnant or nursing,
4. contraindication for TMS or MRI scanning,
5. current substance abuse/dependence,
6. currently taking medications that affects brain structure (e.g. steroids).
Healthy controls with a DSM-5 diagnosis and/or a first-degree relative with a psychotic
disorder. Participants with schizophrenia that are not competent to sign an informed
consent, have more than 12 months antipsychotic exposure, not on the same psychotropic
medications for 4 weeks prior to study, taking clozapine, and not clinically stable (i.e.a
change in psychotic symptoms for at least 4 weeks).
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