Decision-Making in Schizophrenia: a Combined Neuroimaging and Experience Sampling Study
- Conditions
- SchizophreniaSchizoaffective DisorderControl Subjects
- Registration Number
- NCT06745479
- Lead Sponsor
- Rutgers, The State University of New Jersey
- Brief Summary
The goal of this clinical trial is to learn if attention and ways of thinking impact decision-making and brain processes related to decision-making in people with schizophrenia or schizoaffective disorder relative to people without either condition. It will also learn how brain functioning during decision-making relates to real-world decisions made during daily life. The main questions it aims to answer are:
* Does paying attention to specific information impact decision-making and brain processes?
* Does thinking in a certain way according to specific 'thinking strategies' improve brain processes related to decision-making?
* Does brain functioning during decision-making relate to real-world choices to engage in activities?
Researchers will compare brain functioning and decision-making on computer tasks of gambling after participants have been trained to use a positive thinking strategy. They will compare what is different in the brain and behavior when participants use this strategy and when they do not. Participants will also answer brief surveys about activities and feelings for a week in their daily lives.
Participants will:
* Complete several hours of clinical interviewing, cognitive tests, and surveys of about symptoms, experiences, and personality
* Complete computer tasks about gambling decisions during MRI brain scanning and while having their visual attention measured using eye-tracking
* Complete brief surveys about their activities and feelings 5 times a day for 1 week using a cell phone. Each survey only take several minutes.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 74
The following inclusion criteria apply to all subjects:
- Between ages of 18-45.
- Have capacity to provide informed consent
- Fluent communication in English
- Willingness and ability to follow study requirements, as evidenced by an ability to provide written or virtual informed consent and read, and complete, study procedures.
- Cognitive ability to understand tasks and estimated IQ greater than 70.
The following additional inclusion criteria apply to subjects with schizophrenia/schizoaffective disorder:
- Primary diagnosis of schizophrenia or schizoaffective disorder
The following additional inclusion criteria apply to subjects without schizophrenia:
- Inclusion based on subject matched to psychiatric group based on age, sex, race/ethnicity, and education level
The following exclusion criteria apply to all subjects:
- Self-disclosed or noticeable intoxication from alcohol or illicit drugs (e.g., arriving to participate in the study drunk/high)
- Self-disclosure of consistent current substance use other than nicotine, alcohol, or cannabis (e.g. cocaine, heroin).
- Many-year history of severely disordered substance use other than nicotine/tobacco (determined via interview)
- Significant physical health disorder, robust physical health conditions, neurological disease/disorder (e.g., Parkinson's, history of strokes).
- History of traumatic brain injury, head injury resulting in loss of consciousness for an extended duration or with noted neurobehavioral consequences.
- History of electroconvulsive therapy
- History of seizures or epilepsy.
- Currently untreated or unstable psychiatric and medical conditions.
- Intellectual disability
- Contra indications for MR imaging
The following additional exclusion criteria apply to subjects without schizophrenia:
- Pervasive history of problematic substance use (other than nicotine or alcohol) as defined by meeting DSM-5 criteria for a substance use disorder.
- Diagnosis of, or first-degree relative with, significant psychiatric disorder (e.g., bipolar disorder, psychotic disorder, or Cluster A personality disorder).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Nucleus Accumbens Brain Activation Single timeframe during 1.5 hours of MRI scanning and behavioral task completion. Brain activation in the nucleus accumbens (ventral striatum) measured via functional magnetic resonance imaging (fMRI) on trials that are preceded by the cognitive regulation strategy relative to trials without the cognitive regulation strategy.
Gambling Choice Behavior Single timeframe during 1.5 hours of MRI scanning and behavioral task completion. Risky reward pursuit, defined as gamble choices on trials that are preceded by the cognitive regulation strategy relative to trials without the cognitive regulation strategy.
- Secondary Outcome Measures
Name Time Method Brain Activation and Functional Connectivity Single timeframe during 1.5 hours of MRI scanning and behavioral task completion Brain activation and functional connectivity in areas across the whole brain measured via functional magnetic resonance imaging (fMRI) on trials that are preceded by the cognitive regulation strategy relative to trials without the cognitive regulation strategy.
Related Research Topics
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Trial Locations
- Locations (1)
Center for Advanced Human Brain Imaging Research
🇺🇸Piscataway, New Jersey, United States