Characterizing Clinical and Pharmacological Neuroimaging Biomarkers
Overview
- Phase
- Early Phase 1
- Intervention
- MRI
- Conditions
- Cognitive Impairment
- Sponsor
- Yale University
- Enrollment
- 143
- Locations
- 1
- Primary Endpoint
- Working Memory (WM)
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
This study is part of a larger overall study that seeks to characterize clinical and pharmacological neuroimaging biomarkers. The purpose of this registered protocol is understand the effect of emotion on cognitions by specifically examining the effect of reward processing on working memory in patients with schizophrenia.
Detailed Description
Cognition rarely occurs in the 'real world' in isolation, and typically occurs under emotional influences that may alter how cognition occurs. Understanding these motivational and cognitive interactions will help better assess mechanisms that underlie the cognitive and negative symptoms of schizophrenia. To better understand the effect of emotion on cognitions, this study will examine the effect of reward processing on working memory in patients with schizophrenia. To this end, this will be a two-pronged approach. The first prong, is to understand the neural mechanisms of incentivized spatial working memory processes. fMRI will be used and a paradigm will be employed that combines reward processing and working memory to understand how patients with schizophrenia recruit neural systems in response to rewarded working memory. To further understand this, this study will compare the neural effects in patients with schizophrenia with patients with depression, another group of psychiatric patients who also suffer from cognitive and motivational deficits. Both of these groups suffer from cognitive and motivational deficits, yet the treatments and disease presentations differ. It is hypothesized that the ways in which cognitive and motivational processes interact in the brain will have some similarities, but also differences, that distinguish the two psychiatric illnesses. As part of this aim, a group of typical, healthy adults subjects will be recruited as a control. A subset of healthy participants that passed the medical and psychiatric screen will be invited to participate in the ketamine portion of the study which will be completed during the MRI session.
Investigators
Eligibility Criteria
Inclusion Criteria
- •For BOTH Non-Healthy Controls and Healthy Controls:
- •Right-handed as determined by the Edinburgh handedness questionnaire (Oldfield, 1971).
- •Premorbid IQ\>70 determined by WAIS similarities and matrix reasoning subtests; Any history indicating learning disability, mental retardation, or attention deficit disorder will exclude the subject from participation.
- •Must speak or read English at least 8th grade level or higher and to complete study evaluations.
- •Must have intact vision or vision that can be corrected by glasses or contact lenses (corrected 20 20/20).
- •Must be able to tolerate enclosed spaces \*\* only if participating in MRI portion.
- •Female subjects must be postmenopausal for a least 1 year, surgically sterile, or using a reliable method of contraception at screening. Reliable methods of contraception include double-barrier methods (e.g. condom and diaphragm, condom and foam, condom and sponge), intrauterine devices, or hormonal birth control methods. Women with positive serum pregnancy results at screening or self-reporting of pregnancy will be excluded from the study. \*\* only if participating in MRI portion.
- •Must be free of metallic foreign objects in body, such as aneurysm clips or pacemakers, or a questionable history of metallic fragments \*\* only if participating in MRI portion.
- •For Non-Healthy Controls Participants:
- •Adult patients from the community meeting diagnostic criteria for schizophrenia, schizoaffective disorder, psychosis at risk syndrome, Major Depressive Disorder or autism spectrum disorders.
Exclusion Criteria
- •For Healthy Controls:
- •Evidence or history of serious medical or physical conditions, including severe endocrine disorder (Cushing's, Lupus), heart disorder (past history of heart attacks, angina), or other major systemic medical conditions (kidney, MS, CP, blindness, serious physical disability).
- •Neurological conditions that might confound the results, including past stroke, seizures, dementia, brain tumor, brain surgery, neurological disease, head injury, or severe concussion (lasting \>2 minutes in their life).
- •Individual not larger than 55" around shoulders and widest part of chest (approx. 250lb limit) \*\* only if participating in MRI portion.
- •Any other condition that is contra-indicated for fMRI if selected to participate in fMRI portion as determined by the MRRC safety screen. \*\* only if participating in MRI portion.
- •Meeting current diagnostic criteria for any DSM-IV Axis I psychiatric disorders, determined by SCID-NP / MINI interviews.
- •First-degree relative with Axis I DSM-IV disorder.
- •Regular use of psychoactive drugs including anxiolytics and antidepressants.
- •Meeting current DSM-IV abuse and/or dependence diagnostic criteria for other substances, other than nicotine in the past 6 months as determined by SCID-NP / MINI interviews (excluding caffeine).
- •For Non-Healthy Controls:
Arms & Interventions
ASD Patients
This arm consists of patients diagnosed with Autism Spectrum Disorder (ASD) that will receive an MRI.
Intervention: MRI
Schizophrenic Patients
This arm consists of patients diagnosed with Schizophrenia that will receive an MRI.
Intervention: MRI
Healthy Controls
This arm consists of healthy control volunteer participants that will receive an MRI.
Intervention: MRI
Healthy Controls with Ketamine
This arm consists of healthy control volunteer participants that elect to receive ketamine prior to receiving an MRI.
Intervention: MRI
Healthy Controls with Ketamine
This arm consists of healthy control volunteer participants that elect to receive ketamine prior to receiving an MRI.
Intervention: Ketamine
Outcomes
Primary Outcomes
Working Memory (WM)
Time Frame: Up to 2 hours
The tool used to measure working memory (WM) is a spatial working memory task. We measure angular accuracy of spatial working memory, and better accuracy is indicated by a lower angular distance. Subjects are asked to centrally fixate, and a circle appears on the screen briefly, and then disappears. Afterwards they see a gray circle that is linked to a joystick and are asked to move the gray circle to where they best remembered the initial circle to be. We care about the angular distance between where the initial circle appeared and where they placed the gray circle. The low range is 0 degrees, and the high range is 180 degrees. Scores are presented as averages and standard deviations.
Secondary Outcomes
- Behavior(Up to 2 hours)
- BOLD(Up to 2 hours)
- Whole brain connectivity(Up to 2 hours)