NCT06436209

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Mar 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress90%
Mar 2024Jul 2026

Study Start

First participant enrolled

March 27, 2024

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

April 17, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 31, 2024

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2026

Last Updated

August 15, 2025

Status Verified

May 1, 2025

Enrollment Period

2.3 years

First QC Date

April 17, 2024

Last Update Submit

August 12, 2025

Conditions

Keywords

psychological refractory period (PRP), behavioral training, neural representational geometry, lateral prefrontal cortex, separability and generalizability

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

EXPERIMENTAL
Behavioral: Multitask Practice Intervention (MPI)

Single Task Practice

ACTIVE COMPARATOR
Behavioral: Single-task Practice Intervention (SPI)

Interventions

Multitask practice intervention (MPI) includes multiple behavioral testing sessions during which participants receive practice with multitasking two tasks using the psychological refractory period procedure.

Multitask Practice

Single task practice intervention (SPI) includes multiple behavioral testing sessions during which participants receive separate practice on two tasks.

Single Task Practice

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

Metcalf Research Building, Brown University & MRI Research Facility, Brown University

Providence, Rhode Island, 02912, United States

RECRUITING

MeSH Terms

Conditions

Multitasking Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • David Badre, PhD

    Brown University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

David Badre, PhD

CONTACT

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

Locations