Purpose

The purpose of this study is to examine whether cerebellar stimulation can be used to improve cognitive deficits and mood in patients with schizophrenia, autism, bipolar disorder, Parkinson's disease, and major depression.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 90 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • A clinical diagnosis consistent with enrollment

Exclusion Criteria

  • History of recurrent seizures or epilepsy - Any other neurological or psychiatric diagnosis outside the diagnosis for which the participant is enrolled. - Active substance use disorder in the past 6 months other than tobacco use disorder. - Inability to consent for study. - Pacemaker - Coronary Stent - Defibrillator - Neurostimulation - Claustrophobia - Uncontrolled high blood pressure - Atrial fibrillation - Significant heart disease - Hemodynamic instability - Kidney disease - Pregnant, trying to become pregnant, or breast feeding

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Basic Science
Masking
Single (Participant)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
patient active rTMS
Subjects will receive 5 days of 2x daily rTMS targeted over the cerebellum.
  • Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
    Subjects with neuropsychiatric diagnoses and matched-controls will be receive theta frequency stimulation of the cerebellum. We will target the cerebellar vermis.
    Other names:
    • rTMS
Sham Comparator
patient sham rTMS
Subjects will receive 5 days of 2x daily sham stimulation of the cerebellum.
  • Device: Sham Repetitive Transcranial Magnetic Stimulation (rTMS)
    Subjects with neuropsychiatric diagnoses and matched-controls will be receive sham stimulation of the cerebellum. We will target the cerebellar vermis.
    Other names:
    • Sham stimulation
Active Comparator
Control active rTMS
  • Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
    Subjects with neuropsychiatric diagnoses and matched-controls will be receive theta frequency stimulation of the cerebellum. We will target the cerebellar vermis.
    Other names:
    • rTMS
Sham Comparator
Control sham rTMS
  • Device: Sham Repetitive Transcranial Magnetic Stimulation (rTMS)
    Subjects with neuropsychiatric diagnoses and matched-controls will be receive sham stimulation of the cerebellum. We will target the cerebellar vermis.
    Other names:
    • Sham stimulation

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Krystal Parker, PhD

Study Contact

Krystal L Parker, Ph.D
319-353-4554
CT201610712@gmail.com

Detailed Description

Our recent work found that patients with Parkinson's disease and schizophrenia have impaired frontal EEG rhythms in the theta and delta range (1-8 Hz).We have been using transcranial direct current stimulation to recover these rhythms as patients perform elementary cognitive tasks. We found that although we are able to modulate cerebellar and frontal activity with tDCS, this effect is minimal as the depth of the current is not great enough to modulate all cerebellar activity. Here we use transcranial magnetic stimulation (TMS) to modulate neural activity in the frontal cortex and recover cognitive function in patients with autism, schizophrenia, bipolar disorder and Parkinson's disease. The purpose of the study is to explore cerebellar stimulation as a potential new treatment to restore frontal activity and cognitive function in autism, schizophrenia, bipolar disorder and Parkinson's disease.Subjects will be brought in for 5 to 6 separate visits, with cerebellar or sham TMS stimulation twice per day for 5 days, as well as 3 follow-up visits.During these visits the patient will have cognitive, disease-specific and emotional testing, including EEG testing and MRI imaging. For those participants that received sham stimulation we will again use EEG to record how single pulses of magnetic or electrical stimulation influences other regions of the cerebellum and downstream brain regions. These data will provide insight into how the cerebellum may influence downstream brain regions and play a role in cognitive and motor performance. All data will be analyzed offline to determine if performance on the interval timing task and/or frontal brain rhythms change following transcranial magnetic stimulation as compared to the pre-stimulation blocks of trials. Additionally, we will analyze changes in their cognitive function, symptom ratings, functional and structural MRI, and mood following stimulation. Controls will receive both active and sham treatment for comparison.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.