Actively Recruiting
Investigating Mediodorsal Thalamus Representations Underlying Human Cognitive Flexibility
Led by Kai Hwang · Updated on 2026-02-13
100
Participants Needed
1
Research Sites
243 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this basic experimental research study is to examine how the human thalamus supports flexible thinking and behavior. Specifically, the research aims to elucidate how the mediodorsal (MD) thalamus encodes and updates "context"-the mental framework that determines which rules or actions are relevant in a given situation. This work may contribute to understanding why certain psychiatric conditions, such as schizophrenia and ADHD, involve difficulties with cognitive flexibility and control. The primary research questions are: Does the MD thalamus represent the context that organizes how working memory guides task selection? Does the MD thalamus signal when context needs to be updated after a change in task demands? Do these thalamic representations support generalization to new situations or rules? Participants will complete cognitive tasks while undergoing high-resolution brain imaging using 7-Tesla MRI. The investigators will combine behavioral data, computational modeling, and advanced neuroimaging analyses to examine how the thalamus interacts with the cortex during flexible decision-making.
CONDITIONS
Official Title
Investigating Mediodorsal Thalamus Representations Underlying Human Cognitive Flexibility
Who Can Participate
Eligibility Criteria
You may qualify if you...
- No history of any neurological, psychiatric, or medical condition that could affect cognition
- No use of benzodiazepines, long-acting opioids, or other psychotropic drugs that could alter cognitive performance
- Normal or corrected-to-normal vision (visual acuity)
- Normal color perception (Farnsworth-Munsell 100 Hue Test)
- Fluent in English
- No metal implants such as aneurysm clip, cardiac pacemaker, ICD, IUD, neurostimulation system, spinal cord stimulator, internal electrodes or wires, bone stimulator, ear implant, insulin or other infusion pump or device, prosthesis, artificial or prosthetic limb, shunt, vascular access port or catheter, thermodilution catheter, medication patch, radiation seeds or implants, wire mesh implant, tissue expander, surgical staples or clips or sutures, joint replacement, joint/bone pin/screw/nail/wire/plate, dentures, or non-removable hearing aid
- No exposure to shrapnel or other MR contraindications
- No non-removable body piercing jewelry
- No non-removable makeup
- No history of claustrophobia
- No history of breathing problems
- Not currently pregnant or trying to get pregnant (self-reported)
You will not qualify if you...
- History of any neurological, psychiatric, or medical condition that could affect cognition
- Use of benzodiazepines, long-acting opioids, or other psychotropic drugs that could alter cognitive performance
- Not fluent in English
- Known metal implants such as aneurysm clip, cardiac pacemaker, ICD, IUD, neurostimulation system, spinal cord stimulator, internal electrodes or wires, bone stimulator, ear implant, insulin or other infusion pump or device, prosthesis, artificial or prosthetic limb, shunt, vascular access port or catheter, thermodilution catheter, medication patch, radiation seeds or implants, wire mesh implant, tissue expander, surgical staples or clips or sutures, joint replacement, joint/bone pin/screw/nail/wire/plate, dentures, or non-removable hearing aid
- History of claustrophobia
- Currently pregnant or trying to get pregnant (self-reported)
AI-Screening
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Trial Site Locations
Total: 1 location
1
The University of Iowa
Iowa City, Iowa, United States, 52242
Actively Recruiting
Research Team
K
Kai Hwang, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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