Cognitive Control & the Functional Organization of the Frontal Cortex
2 other identifiers
interventional
60
1 country
1
Brief Summary
The goal of this basic experimental clinical trial is to understand the effect of multitasking practice on the structure of neural representations of tasks in the human lateral prefrontal cortex and control brain regions. The main question it aims to answer is: What changes in neural representational structure predict improvements in multitasking behavior due to multitasking practice? Healthy human participants will learn two independent tasks, each mapping a set of stimuli to motor responses based on different rules. Participants will be randomized to one of two interventions. Participants assigned to the multitask practice intervention (MPI) will practice multitasking the two tasks over multiple days. Those assigned to the single-task practice intervention (SPI) will instead practice each task separately while controlling for the total number of practice opportunities associated with each task across the interventions. Both before and after the practice, the ability of all participants to perform both tasks simultaneously will be behaviorally measured using a well-established psychological refractory period (PRP) paradigm, and their neural representations will be measured using functional MRI while they perform the two tasks. Researchers will then compare improvements in multitasking behavior across the two groups, as well as changes in neural representational geometry of the tasks in the lateral prefrontal cortex and control brain regions, and test whether multitasking training is associated with specific changes in neural representations in the lateral prefrontal cortex.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 27, 2024
CompletedFirst Submitted
Initial submission to the registry
April 17, 2024
CompletedFirst Posted
Study publicly available on registry
May 31, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 31, 2026
August 15, 2025
May 1, 2025
2.3 years
April 17, 2024
August 12, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Effect of the practice intervention on change in overall and task-relevant neural separability in lateral prefrontal cortex
Overall neural separability (also referred to as shattering dimensionality) will be measured by employing cross-validated neural decoding of lateral PFC fMRI BOLD multi-voxel patterns, averaging decoding accuracies across all balanced dichotomies of the task inputs. Task-relevant neural separability will be measured by averaging decoding accuracies across all task-relevant variables.
through study completion, an average of 1.5 years
Effect of multitasking practice on behavioral multitasking cost
Behavioral multitasking cost will be estimated by computing the difference in mean response time on task 2 on long SOAs and short SOAs in the Psychological Refractory Period paradigm. The effect of multitasking practice on behavioral multitasking will be estimated using linear mixed-effects regression, and is defined as the regression weight associated with the interaction effect of time point and intervention on multitasking cost.
through study completion, an average of 1.5 years
Contribution of overall and task-relevant neural separability in lateral prefrontal cortex to the effect of multitasking practice on behavioral multitasking cost
The contribution of prefrontal neural separability change to the effect of multitasking practice on behavioral multitasking will be estimated using linear mixed-effects regression, and is defined as the regression weight associated with the interaction effect of time point, intervention and separability on multitasking cost.
through study completion, an average of 1.5 years
Secondary Outcomes (2)
Cross-classification generalization performance of task-relevant variables in lateral prefrontal cortex
through study completion, an average of 1.5 years
Coding axis angles between stimulus feature representations in two tasks in lateral prefrontal cortex
through study completion, an average of 1.5 years
Study Arms (2)
Multitask Practice
EXPERIMENTALSingle Task Practice
ACTIVE COMPARATORInterventions
Multitask practice intervention (MPI) includes multiple behavioral testing sessions during which participants receive practice with multitasking two tasks using the psychological refractory period procedure.
Single task practice intervention (SPI) includes multiple behavioral testing sessions during which participants receive separate practice on two tasks.
Eligibility Criteria
You may qualify if:
- Normal or corrected to normal vision.
You may not qualify if:
- Left handedness
- Presence or history of neurological or psychiatric disorders
- Usage of brain related medications
- Previous head injury and time spent unconscious
- Any implanted medial fragment or device in the body of the participant.
- Tattoos above the neck
- Injury to the eye or other body part involving a metallic object or fragment.
- Welding, grinding, or cutting of metal in lifetime of participant without usage of safety protection glasses.
- injury to the participant by a metallic object or foreign body (e.g., BB, bullet, shrapnel, etc.)
- Pregnancy or possibility of pregnancy
- Implants or devices including:
- Electronic implant or device, Magnetically-activated implant or device, Cardiac pacemaker, Implanted cardioverter defibrillator (ICD), Aneurysm clip(s), Neurostimulation system, Spinal cord stimulator, Internal electrodes or wires, Bone growth/bone fusion stimulator, Cochlear, otologic, or other ear implant, Insulin or infusion pump, Implanted drug infusion device, Any type of prosthesis (eye, penile, etc.), Heart valve prosthesis, Eyelid spring or wire, Artificial or prosthetic limb, Metallic stent, filter, or coil, Shunt (spinal or intraventricular), Vascular access port and/or catheter, Radiation seeds or implants, Swan-Ganz or triple lumen catheter, Medication patch (Nicotine,Nitroglycerine), Any metallic fragment or foreign body, Wire mesh implant, Tissue expander (e.g., breast), Surgical staples, clips, or metallic sutures Joint replacement (hip, knee, etc.) Bone/joint pin, screw, nail, wire, plate, etc. IUD or diaphragm, Dentures or partial plates, Tattoo or permanent makeup above the neck, Body piercing jewelry that can not be removed, Breathing disorder, Motion disorder or tremors, Claustrophobia, Hearing aid
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Brown Universitylead
- National Institute of Mental Health (NIMH)collaborator
Study Sites (1)
Metcalf Research Building, Brown University & MRI Research Facility, Brown University
Providence, Rhode Island, 02912, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David Badre, PhD
Brown University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 17, 2024
First Posted
May 31, 2024
Study Start
March 27, 2024
Primary Completion (Estimated)
July 31, 2026
Study Completion (Estimated)
July 31, 2026
Last Updated
August 15, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will share