- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01550211
Changes in Brain Synchronization During Perceptual and Linguistic Tasks in Schizophrenic Patients
This study aims to identify electrophysiological correlates of impaired perceptual and linguistic processes in chronic schizophrenic patients, un-medicated first-episode schizophrenic patients and their healthy relatives.
Following administrating some questionnaires (demographic details and psychiatric history questionnaire, handedness questionnaire, reading abilities test and positive and negative symptoms questionnaire) and performing a perception test and a verbal abstract intelligence test, participants will conduct a brain scan during a series of perceptual and linguistic tasks.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Maor Zeev-Wolf, M.A.
- Phone Number: 972-50-7737032
- Email: maorwolf@gmail.com
Study Locations
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-
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Hod-Hasharon, Israel
- Shalvata MHC
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Contact:
- Maor Zeev-Wolf, M.A.
- Phone Number: 972-50-7737032
- Email: maorwolf@gmail.com
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Sub-Investigator:
- Maor Zeev-Wolf, M.A.
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
- Chronic patients - Up to 30 chronic schizophrenic patients.
- Naive patients - Up to 30 unmedicated first episode schizophrenic patients.
- Patients' relatives - Up to 60 family members (parents or siblings) of the participants - control group 1.
- Students - Up to 30 students from Bar-Ilan University - control group 2.
Description
Inclusion Criteria:
Inclusion criteria for chronic patients:
- Hebrew native speakers.
- Diagnosis of schizophrenia with a history of more than one episode.
- Capable and willing to provide informed consent.
Inclusion criteria for naive patients:
- Hebrew native speakers.
- Diagnosis of schizophrenia with a history of only one episode and unmedicated.
- Capable and willing to provide informed consent.
Inclusion criteria for patients' relatives (control group 1):
- Hebrew native speakers.
- Without any psychiatric history.
- Have a child and/or a sibling with schizophrenia.
Inclusion Criteria for students (control group 2):
- Hebrew native speakers.
- Without any psychiatric history.
Exclusion Criteria:
Exclusion Criteria for patient groups (chronic and "naïve"):
- Left handedness.
- Reading disability.
- Visual perception disability.
- Brain damage and/or a history of seizures.
- Impaired intelligence.
- Metal implants.
Exclusion Criteria for control groups (family members and students):
- Psychiatric history.
- Left handedness.
- Reading disability.
- Visual perception disability.
- Brain damage and/or a history of seizures.
- Impaired intelligence.
- Metal implants.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Students
Healthy students from Bar-Ilan University
|
Conducting a brain scan during a series of perceptual and linguistic tasks
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Schizophrenic patients' relatives
Healthy family members (parents or siblings) of the schizophrenic participants (chronic and naive)
|
Conducting a brain scan during a series of perceptual and linguistic tasks
|
Naive schizophrenic patients
Naive patients with a diagnosis of schizophrenia, a history of only one psychotic episode and un-medicated
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Conducting a brain scan during a series of perceptual and linguistic tasks
|
Chronic schizophrenia patients
Chronic patients with a diagnosis of schizophrenia and a history of more than one psychotic episode
|
Conducting a brain scan during a series of perceptual and linguistic tasks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Magnetic field amplitude and source
Time Frame: 45 minutes
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45 minutes
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Hilik Levkovitz, Professor, Shalvata MHC
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
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
Other Study ID Numbers
- SHA-0001-12
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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