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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00418652
Other study ID # SHEBA-06-4252-RA-CTIL
Secondary ID
Status Completed
Phase N/A
First received January 4, 2007
Last updated August 3, 2011
Start date January 2006

Study information

Verified date August 2011
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

Trans Cranial Magnetic Stimulation (TMS) over dorsal visual system will disturb the ability to identify objects with decreased level of fragmentation


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.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date
Est. primary completion date July 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Normal controls

Exclusion Criteria:

- neurological, ophthalmological or psychiatric problems

- family history of schizophrenia

- left handed

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
No TMS intervention
In the "no TMS" condition, no simulation was given and no coil placed near participants' heads.
TMS over the PO3 EEG site
10Hz TMS over the dorsal stream (PO3 EEG site)
TMS over the vertex
10Hz TMS for over vertex.

Locations

Country Name City State
Israel Psychiatry Clinic - Sheba Medical Center Tel-hashomer

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Results of the study assignments performed by the participants during the study. 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 No
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