The Computational and Neural Mechanisms Linking Decision-making and Memory in Humans

Sponsor
Icahn School of Medicine at Mount Sinai (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06072378
Collaborator
National Institute of Mental Health (NIMH) (NIH)
25
1
1
22
1.1

Study Details

Study Description

Brief Summary

Learning to make good decisions in the present, and accurately recalling events and information from the past, are critical aspects of human cognition that are often impaired in many psychiatric disorders. This project aims to identify the how the choices individuals make influence what, and how, people remember by combining disparate techniques in computational modeling and direct brain recordings in human subjects. The researcher developed a dual-task paradigm, probing how decisions in one task affect immediate recognition memory. To examine the neural mechanisms underlying model-free RL's influence on memory, the researcher will record local field potential (LFP) and single neuron activity in various brain regions as epilepsy patients perform the proposed task. The results of this project will identify specific neurocomputational mechanisms unifying decision-making and memory processes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Value-manipulation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
25 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
The Computational and Neural Mechanisms Linking Decision-making and Memory in Humans
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2025
Anticipated Study Completion Date :
Aug 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Value-manipulation

Participants with epilepsy will complete a behavioral task in which they use a laptop computer to do a decision-making and memory task.

Behavioral: Value-manipulation
During the decision-making task, different choices are assigned different values probabilistically.

Outcome Measures

Primary Outcome Measures

  1. Local-field potentials changes [During task participation, approx. 30-45 min in the first 2 weeks of hospital stay]

    Detection of local-field potentials (LFPs) in the various regions (hippocampus, amygdala, and frontal cortex). Local field potentials are the biological voltages recorded by macroelectrodes implanted in participant's subcortical regions as part of their treatment for epilepsy. LFP changes (measured as increases or decreases in voltage) as a function of participant behavior will be recorded, and in response to the task manipulation of the value of choices during the decision-making task

  2. Firing rate changes [During task participation, approx. 30-45 min in the first 2 weeks of hospital stay]

    Single-neuron activity recorded from the hippocampus, amygdala, and frontal cortex. Single-neuron activity refers the micro-scale changes in single-neuron action potentials recorded by microelectrodes implanted in subcortical regions. Firing rate changes (measured as difference in spikes/seconds [Hz]) will be reported for neurons as a function of how behavior changes when the value of choices is altered.

Secondary Outcome Measures

  1. Reaction time [During task participation, approx. 30-45 min in the first 2 weeks of hospital stay]

    Reaction times involve measuring how quickly the participant makes each choice during the decision-making and memory tasks, in milliseconds. This will be recorded by logging keypresses and mouse inputs to the behavioral computers. Slow reaction times indicate increased cognitive processing.

  2. Number of hit rates for decision-making [During task participation, approx. 30-45 min in the first 2 weeks of hospital stay]

    Choices in decision-making task involved logging the decision-making selections that participants make. This will be recorded by logging keypresses and mouse inputs (left or right) to the behavioral computers. This will be used to track whether participants decisions change when value manipulations occur.

  3. Number of hit rates for Memory performance [During task participation, approx. 30-45 min in the first 2 weeks of hospital stay]

    Memory performance involved logging the memory-recognition selections that participants make. This will be recorded by logging keypresses and mouse inputs (old or new) to the behavioral computers. This will be used to track whether participants memory performance changes when value manipulations occur.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Has seizure activity which is deemed non-responsive to standard pharmacological intervention(s), as determined by treating Neurologist and established clinical practices

  • Has elected to receive clinically indicated intracranial EEG (electrocorticography (ECoG), stereoelectroencephalography (SEEG)) and/or temporal responsive neurostimulation (RNS) for medication-refractory epilepsy outside of this research study, as determined by treating clinician(s) and per current clinical practice

  • Capacity to provide written informed consent

  • Language proficiency in English or Spanish

  • Willing and able to comply with all study-related procedures

Exclusion Criteria:
  • History of psychosis, such as in the context of depressive or manic episode.

  • Active suicidal ideation with intent, suicide attempt within the last six months, or other serious suicide risk

  • Inability to provide informed consent or reliably participate in study assessments, as per the Montreal Cognitive Assessment (MOCA; score < 26) or in the opinion of the evaluating neuropsychologist.

  • Individuals unwilling or unable to undergo electrode implantation procedures

  • Medical contraindications to neurosurgery or for general anesthesia, neurosurgery, or an MRI scan (required for electrode implantation)

  • Neurological disorder other than epilepsy or other significant brain pathology, if contraindicated in the opinion of implanting neurosurgeon.

  • Women who are pregnant

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mount Sinai West New York New York United States 10024

Sponsors and Collaborators

  • Icahn School of Medicine at Mount Sinai
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Salman E Qasim, PhD, Icahn School of Medicine at Mt. Sinai

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Salman E Qasim, Postdoctoral Fellow, Icahn School of Medicine at Mount Sinai
ClinicalTrials.gov Identifier:
NCT06072378
Other Study ID Numbers:
  • GCO 22-1028
  • K99MH132873
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 10, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No

Study Results

No Results Posted as of Oct 10, 2023