Brain Imaging of Cognition Inn Schizophrenia and Depression
NCT ID: NCT04159662
Last Updated: 2024-04-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
90 participants
OBSERVATIONAL
2019-12-12
2026-10-01
Brief Summary
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Detailed Description
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The study will involve three visits at The Royal's Institute of Mental Health Research. Each visit will last about 2.5 hours long.
Visits 1 and 2: We ask participants to fill out several questionnaires on a computer. We also ask participants to answer some questions about their current and past mental health. Participants will also perform some tasks involving general thinking skills.
Visit 3: This is the scan visit where we use fMRI, which is a technique that allows us to take a 3D picture of the brain using magnetic fields. It also allows us to estimate how active different regions of the brain are. During the fMRI, participants will lay down in a narrow tube in the fMRI scanner and hold still. Throughout the experiment, participant will perform three short tasks in the scanner, where they will see words and pictures and press a button to answer some questions.
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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Individuals with Schizophrenia or Schzioaffective Disorders
Clinical group
No interventions assigned to this group
Individuals with Major Depressive Disorder
Clinical group
No interventions assigned to this group
Healthy Individuals
Control group
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* current Intelligence Quotient (IQ) \> 70 as measured by the Wechsler Abbreviated Scale of Intelligence (WASI)
* the ability to read and speak fluent English
* a diagnosis of schizophrenia, schizoaffective or major depression disorder
* stable medication for more than one month
Exclusion Criteria
* a recent history of substance abuse or dependence (within the past 3 months)
* any magnetic resonance imaging (MRI) contraindications (e.g. metallic head implant, history of seizure, pacemaker)
* decisional incapacity requiring a guardian
* taking medications that are rated as Anticholinergic Burden (ACB) Score 3 (severe) or taking benzodiazepines on a daily basis
18 Years
65 Years
ALL
No
Sponsors
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The Royal Ottawa Mental Health Centre
OTHER
Responsible Party
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Synthia Guimond
Scientist
Principal Investigators
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Synthia Guimond, PhD
Role: PRINCIPAL_INVESTIGATOR
Royal Ottawa Mental Health Centre
Locations
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Royal Ottawa Mental Health Center
Ottawa, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2018037
Identifier Type: -
Identifier Source: org_study_id
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