- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00418652
Interruption of Dorsal Visual Stream Using TMS
Interruption of Dorsal Visual Stream Using TMS in Normal Controls
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The participants performed two tasks under three different TMS conditions: no TMS, 10Hz TMS for over the dorsal stream (PO3 EEG site) or over the vertex.
First they performed a perceptual closure task which asked them to identify an object in a series of six progressively less degraded pictures.
Then, they also performed a control task previously shown not to be mediated by the LOC and not to be impaired in schizophrenia: The perception of illusory contours.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Tel-hashomer, Israel, 52621
- Psychiatry Clinic - Sheba Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Normal controls
Exclusion Criteria:
- neurological, ophthalmological or psychiatric problems
- family history of schizophrenia
- left handed
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: No TMS stimulation
The patients performed 2 tasks: a study and a control assignments with no TMS stimulation.
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In the "no TMS" condition, no simulation was given and no coil placed near participants' heads.
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Experimental: TMS over the dorsal stream
The patients performed 2 tasks: a study and a control assignments under TMS stimulation over the dorsal stream area (PO3 EEG site).
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10Hz TMS over the dorsal stream (PO3 EEG site)
Other Names:
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Sham Comparator: TMS over the vertex
The patients performed 2 tasks: a study and a control assignments under TMS stimulation over the vertex area.
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10Hz TMS for over vertex.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Results of the study assignments performed by the participants during the study.
Time Frame: The participants performed the tasks once during their study visit
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The subjects performed 2 tasks: The primary dependent measures consisted of the level of detail needed for correct object identification, response accuracy, and response time in milliseconds for correct responses. Illusory Contour Task: Subjects also performed a pulsed pedestal task, Participants were shown 55 drawings for 500 ms each. Some drawings contained partial contours which defined a geometric shape, while in others the contours did not define a shape. Participants were asked to indicate whether they recognized a geometric shape or not. Accuracy and response time were measured. |
The participants performed the tasks once during their study visit
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Revital Amiaz, MD, Sheba Medical Center
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SHEBA-06-4252-RA-CTIL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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