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NCT07217652Recruiting

Investigating Mediodorsal Thalamus Representations Underlying Human Cognitive Flexibility

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
10 Oct 2025
Start date
1 Dec 2025
Primary completion date
30 Jun 2030
Lead sponsor
Kai Hwang
NCT number
NCT07217652

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 1 Dec 2025 to the primary completion date, 30 Jun 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of benzodiazepines, long-acting opioids, or other psychotropic drugs that could alter cognitive performance

Other illness

  • Has a history of any neurological, psychiatric, or medical condition that could affect cognition
  • Known metal implants (including 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

Other

  • Not fluent in English
  • Currently pregnant or trying to get pregnant (this will be determined via self report and no records will be kept).

Who the study is looking for

  • 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 (including 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-related 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 (this will be determined via self report and no records will be kept).

Age in the registry: 18 years to 35 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Iowa
Coordinator of this site? Confirm its status
Iowa CityUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.