Viewing Study NCT06436209



Ignite Creation Date: 2024-06-16 @ 11:49 AM
Last Modification Date: 2025-12-17 @ 3:12 AM
Study NCT ID: NCT06436209
Status: None
Last Update Posted: 2025-08-15 00:00:00
First Post: 2024-04-17 00:00:00

Brief Title: Cognitive Control & the Functional Organization of the Frontal Cortex
Sponsor: Brown University
Organization: Brown University

Study Overview

Official Title: Cognitive Control & the Functional Organization of the Frontal Cortex
Status: None
Status Verified Date: 2025-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Background and Study Rationale:

Human performance on a task deteriorates when it is performed concurrently with another task. This multitasking cost has been attributed to competition for shared computational or biological resources and there is considerable debate in the field about the specific nature of these putative resources. Extensive multitasking practice is known to reduce, and sometimes, abolish these costs. These practice-related gains have been attributed to changes in central processing, more efficient task scheduling, or the learning of specialized task representations. The human prefrontal cortex is critical to flexible cognitive control of behavior, and is involved in representing tasks. However, it remains unknown what effect multitasking practice has on prefrontal task representations. In this study, we will directly address a gap in our knowledge by testing the link between multitasking costs and the geometry of neural manifolds representing task inputs in the lateral PFC.

Study Design:

Overview:

This study is a single-center, randomized controlled trial designed to examine the effect of multitask practice on multitasking behavior, the geometry of neural representations of tasks in the lateral prefrontal cortex and the relationship between these effects. A total of 60 healthy subjects are planned, 30 subjects being randomized to each, the multitask practice group (MPG), and the single task practice group (SPG). Baseline and endline assessments of multitasking behavior and neural representations in lateral PFC with fMRI will be conducted in all subjects.

Study Treatments:

Single-task practice treatment:

The single-task practice treatment will involve 3 sessions of practice during which subjects will practice instructed tasks in individual task blocks. Up to 48 blocks of practice will be performed. Subjects will be given feedback at the end of each block on their accuracy and speed of responding and they will be given an improvement target.

Multitask practice treatment:

The multitask practice treatment will involve 3 sessions of practice during which subjects will practice instructed tasks in the psychological refractory period paradigm. Up to 48 blocks of practice will be performed. Subjects will be given feedback at the end of each block on their accuracy and speed of responding and they will be given an improvement target.

Subject Selection:

Subjects will be recruited from the Providence community. Subjects will be screened over a phone call. Inclusion criteria include right-handedness, age between 18 and 35, and normal or corrected-to-normal vision. Exclusion criteria include history of psychiatric or neurological deficits and MR contraindications. Consenting procedures will be conducted in person during Study Session 1 and continuing consent will be periodically obtained during all lab Study visits.

Random Assignment:

Up to 60 eligible patients will be randomly assigned to SPG or MPG treatment groups in a 1:1 ratio by using a random number generator coded in MATLAB. Neither the experimenters nor the study subjects, will be blinded to the assignment.

Study Structure:

A total of 14 study sessions are planned for each subject. Study session 1 will be employed for informed consent, scheduling and familiarization with study tasks. Baseline evaluations will take place during study sessions 2 through 5. Treatment will be administered during study sessions 6 through 8 during which subjects will receive either 3 sessions of multi-task practice (MPG) or 3 sessions of single-task practice (SPG). Endline evaluations will take place during study sessions 9 through 12. Detailed descriptions of each Study session and all paradigms used for measurements are given below.

Behavioral paradigms:

All behavioral task paradigms will be implemented using Psychtoolbox 3 in MATLAB or in JSPsych. All tasks involve responding to visual objects presented on a computer screen with keypresses either on a keyboard or on a response box. Visual objects will vary along 4 dimensions - shape (square or circle), circle (orange or blue), pattern (dotted or striped) or size (small or large). Along with the visual object, a response panel consisting of the symbols @ and #. Subjects will be introduced to three different tasks: the shape task, color task and the pattern task. In each task, they will make a binary classification of the visual object relying on the relevant task feature (e.g. color in the color task). Each binary class will be associated with one of two categories associated with the @ and # symbols. Subjects will then select the response key associated with the relevant symbol. The left-right position of the two symbols will be varied randomly from trial to trial such that the position would be the same as the previous trial on approximately 50% of the trials, and each trial-type was associated with an equal number of left and right responses.

Single task paradigm: In the single-task paradigm, visual objects will be presented for up to 2.2 s. Responses deadline is 2.2s. Inter-trial interval will be 1 s. Trials are presented in pure single-task blocks with 64 trials per block.

Mixed tasks paradigm: In the mixed tasks paradigm, visual objects will be presented for up to 2.2 s. Response deadline is 2.2s. Inter-trial interval will be jittered between 2 and 10 seconds. Trials of multiple task types will be presented in the same block, with a word cue identifying the task to be performed on every trial.

Psychological Refractory Period paradigm: In the PRP paradigm, two visual objects will be presented on every trial, one in the upper half of the screen, and the other in the bottom half of the screen. Visual objects will be presented with a stimulus onset synchrony (SOA) varying between 50 ms and 1.5 s. Trial length will be up to 3 s. Response deadline will be 3 s for responding to both visual objects. Inter-trial interval will be either 1 s (behavioral blocks) or jittered between 2 and 10 seconds (MRI blocks). Subjects will be instructed to perform the tasks in a specific order (e.g. Color, then Shape), responding to the first stimulus that appears with the rule associated with the first task in the order and to the object that appears second. A total of 3 different task orders will be presented to subjects (e.g. Color -\> Shape, Shape -\> Color and Color -\> Pattern) and these orders will be counterbalanced across subjects such that each task has placed every role equally in each treatment group. All task orders will be administered during both baseline and endline.

MRI Protocol:

Each subject will under MRI procedures during Study Visits 2, 3, 9 and 10. Each visit will last 2 hrs during which subjects will first be provided refresher instruction on the behavioral tasks before undergoing MRI for 1 hr. During each 1 hr MRI scanning session, subjects will first be screened for metal, briefed on safety procedures and motion minimization requirements, and then situated on the scanning table in a supine position. Their head will be stabilized with soft padding, and their ears will be protected from MR noise with ear plugs. Subjects will view a computer screen through a mirror installed on a headstage and will be provided with two response boxes for performing the tasks and an emergency buzzer for communicating with the experimenters and radiographers on duty. They will then undergo a multiple echo MPRAGE scan (repetition time (TR) = 2530 ms, echo times (TE) = 1.69, 3.55, 5.41, and 7.27 ms, flip angle = 7 degrees, 176 sagittal slices, 1 × 1 × 1 mm voxels) for 6 minutes during which they may close their eyes. Following this, subjects will undergo 5-10 runs of Echo Planar Imaging (TR = 1000 ms, TE = 32.6 ms, flip angle = 64, SMS = 5, Echo spacing 0.59, 65 interleaved slices with voxel size of 2.4mm x 2.4mm x 2.4mm), each lasting between 4 to 9 minutes, during which they will perform multiple blocks of either the mixed tasks paradigm (Days 2 and 9) or the PRP paradigm (Days 3 and 10).

Study Session Descriptions:

Study Session 1:

During Study session 1, subjects will go through the consenting process with a trained research assistant. After informed consent is provided, subjects will be given an overview of the study and they will be introduced to the basic task procedure and the color, shape and pattern rules. They will practice each task in the single task paradigm for 2 blocks each. Following this they will be introduced to the PRP paradigm with their assigned task orders, for 6 blocks. At the end of the session, subjects will be debriefed and remunerated for their participation.

Study Session 2:

During Study session 2, subjects will undergo baseline measurements with the PRP paradigm with their assigned task orders, for 12 blocks. At the end of the session, subjects will be debriefed and remunerated for their participation.

Study Session 3:

During Study session 3, subjects will undergo baseline measurements with the Mixed tasks paradigm for 12 blocks. At the end of the session, subjects will be debriefed and remunerated for their participation.

Study Session 4:

During Study session 4, subjects will undergo baseline measurements of the neural representations of tasks. The MRI protocol will be administered with the Mixed tasks paradigm.

Study Session 5:

During Study session 5, subjects will undergo baseline measurements of the neural representations of tasks. The MRI protocol will be administered with the PRP paradigm.

Study Sessions 6-8:

Subjects will be administered the treatment during these sessions. The single-task practice treatment group will receive 12-24 blocks of practice with the single task paradigm and they will be provided feedback on their performance after every block along with targets for improvement. The multi-task practice treatment will practice one of the three orders in the PRP paradigm across 12-24 blocks Subjects will be given feedback at the end of each block on their accuracy and speed of responding and they will be given an improvement target.

Study Session 9:

During Study session 9, subjects will undergo endline measurements with the PRP paradigm with their assigned task orders, for 12 blocks. At the end of the session, subjects will be debriefed and remunerated for their participation.

Study Session 10:

During Study session 10, subjects will undergo endline measurements with the Mixed tasks paradigm for 12 blocks. At the end of the session, subjects will be debriefed and remunerated for their participation.

Study Session 11:

During Study session 11, subjects will undergo endline measurements of the neural representations of tasks. The MRI protocol will be administered with the Mixed tasks paradigm.

Study Session 12:

During Study session 12, subjects will undergo endline measurements of the neural representations of tasks. The MRI protocol will be administered with the PRP paradigm.
Detailed Description: Background and Study Rationale

Human performance on a task deteriorates when it is performed concurrently with another task This multitasking cost has been attributed to competition for shared computational or biological resources and there is considerable debate in the field about the specific nature of these putative resources Extensive multitasking practice is known to reduce and sometimes abolish these costs These practice-related gains have been attributed to changes in central processing more efficient task scheduling or the learning of specialized task representations The human prefrontal cortex is critical to flexible cognitive control of behavior and is involved in representing tasks However it remains unknown what effect multitasking practice has on prefrontal task representations In this study we will directly address a gap in our knowledge by testing the link between multitasking costs and the geometry of neural manifolds representing task inputs in the lateral PFC

Study Design

Overview

This study is a single-center randomized controlled trial designed to examine the effect of multitask practice on multitasking behavior the geometry of neural representations of tasks in the lateral prefrontal cortex and the relationship between these effects A total of 60 healthy subjects are planned 30 subjects being randomized to each the multitask practice group MPG and the single task practice group SPG Baseline and endline assessments of multitasking behavior and neural representations in lateral PFC with fMRI will be conducted in all subjects

Study Treatments

Single-task practice treatment

The single-task practice treatment will involve 3 sessions of practice during which subjects will practice instructed tasks in individual task blocks Up to 48 blocks of practice will be performed Subjects will be given feedback at the end of each block on their accuracy and speed of responding and they will be given an improvement target

Multitask practice treatment

The multitask practice treatment will involve 3 sessions of practice during which subjects will practice instructed tasks in the psychological refractory period paradigm Up to 48 blocks of practice will be performed Subjects will be given feedback at the end of each block on their accuracy and speed of responding and they will be given an improvement target

Subject Selection

Subjects will be recruited from the Providence community Subjects will be screened over a phone call Inclusion criteria include right-handedness age between 18 and 35 and normal or corrected-to-normal vision Exclusion criteria include history of psychiatric or neurological deficits and MR contraindications Consenting procedures will be conducted in person during Study Session 1 and continuing consent will be periodically obtained during all lab Study visits

Random Assignment

Up to 60 eligible patients will be randomly assigned to SPG or MPG treatment groups in a 11 ratio by using a random number generator coded in MATLAB Neither the experimenters nor the study subjects will be blinded to the assignment

Study Structure

A total of 14 study sessions are planned for each subject Study session 1 will be employed for informed consent scheduling and familiarization with study tasks Baseline evaluations will take place during study sessions 2 through 5 Treatment will be administered during study sessions 6 through 8 during which subjects will receive either 3 sessions of multi-task practice MPG or 3 sessions of single-task practice SPG Endline evaluations will take place during study sessions 9 through 12 Detailed descriptions of each Study session and all paradigms used for measurements are given below

Behavioral paradigms

All behavioral task paradigms will be implemented using Psychtoolbox 3 in MATLAB or in JSPsych All tasks involve responding to visual objects presented on a computer screen with keypresses either on a keyboard or on a response box Visual objects will vary along 4 dimensions - shape square or circle circle orange or blue pattern dotted or striped or size small or large Along with the visual object a response panel consisting of the symbols and Subjects will be introduced to three different tasks the shape task color task and the pattern task In each task they will make a binary classification of the visual object relying on the relevant task feature eg color in the color task Each binary class will be associated with one of two categories associated with the and symbols Subjects will then select the response key associated with the relevant symbol The left-right position of the two symbols will be varied randomly from trial to trial such that the position would be the same as the previous trial on approximately 50 of the trials and each trial-type was associated with an equal number of left and right responses

Single task paradigm In the single-task paradigm visual objects will be presented for up to 22 s Responses deadline is 22s Inter-trial interval will be 1 s Trials are presented in pure single-task blocks with 64 trials per block

Mixed tasks paradigm In the mixed tasks paradigm visual objects will be presented for up to 22 s Response deadline is 22s Inter-trial interval will be jittered between 2 and 10 seconds Trials of multiple task types will be presented in the same block with a word cue identifying the task to be performed on every trial

Psychological Refractory Period paradigm In the PRP paradigm two visual objects will be presented on every trial one in the upper half of the screen and the other in the bottom half of the screen Visual objects will be presented with a stimulus onset synchrony SOA varying between 50 ms and 15 s Trial length will be up to 3 s Response deadline will be 3 s for responding to both visual objects Inter-trial interval will be either 1 s behavioral blocks or jittered between 2 and 10 seconds MRI blocks Subjects will be instructed to perform the tasks in a specific order eg Color then Shape responding to the first stimulus that appears with the rule associated with the first task in the order and to the object that appears second A total of 3 different task orders will be presented to subjects eg Color - Shape Shape - Color and Color - Pattern and these orders will be counterbalanced across subjects such that each task has placed every role equally in each treatment group All task orders will be administered during both baseline and endline

MRI Protocol

Each subject will under MRI procedures during Study Visits 2 3 9 and 10 Each visit will last 2 hrs during which subjects will first be provided refresher instruction on the behavioral tasks before undergoing MRI for 1 hr During each 1 hr MRI scanning session subjects will first be screened for metal briefed on safety procedures and motion minimization requirements and then situated on the scanning table in a supine position Their head will be stabilized with soft padding and their ears will be protected from MR noise with ear plugs Subjects will view a computer screen through a mirror installed on a headstage and will be provided with two response boxes for performing the tasks and an emergency buzzer for communicating with the experimenters and radiographers on duty They will then undergo a multiple echo MPRAGE scan repetition time TR 2530 ms echo times TE 169 355 541 and 727 ms flip angle 7 degrees 176 sagittal slices 1 1 1 mm voxels for 6 minutes during which they may close their eyes Following this subjects will undergo 5-10 runs of Echo Planar Imaging TR 1000 ms TE 326 ms flip angle 64 SMS 5 Echo spacing 059 65 interleaved slices with voxel size of 24mm x 24mm x 24mm each lasting between 4 to 9 minutes during which they will perform multiple blocks of either the mixed tasks paradigm Days 2 and 9 or the PRP paradigm Days 3 and 10

Study Session Descriptions

Study Session 1

During Study session 1 subjects will go through the consenting process with a trained research assistant After informed consent is provided subjects will be given an overview of the study and they will be introduced to the basic task procedure and the color shape and pattern rules They will practice each task in the single task paradigm for 2 blocks each Following this they will be introduced to the PRP paradigm with their assigned task orders for 6 blocks At the end of the session subjects will be debriefed and remunerated for their participation

Study Session 2

During Study session 2 subjects will undergo baseline measurements with the PRP paradigm with their assigned task orders for 12 blocks At the end of the session subjects will be debriefed and remunerated for their participation

Study Session 3

During Study session 3 subjects will undergo baseline measurements with the Mixed tasks paradigm for 12 blocks At the end of the session subjects will be debriefed and remunerated for their participation

Study Session 4

During Study session 4 subjects will undergo baseline measurements of the neural representations of tasks The MRI protocol will be administered with the Mixed tasks paradigm

Study Session 5

During Study session 5 subjects will undergo baseline measurements of the neural representations of tasks The MRI protocol will be administered with the PRP paradigm

Study Sessions 6-8

Subjects will be administered the treatment during these sessions The single-task practice treatment group will receive 12-24 blocks of practice with the single task paradigm and they will be provided feedback on their performance after every block along with targets for improvement The multi-task practice treatment will practice one of the three orders in the PRP paradigm across 12-24 blocks Subjects will be given feedback at the end of each block on their accuracy and speed of responding and they will be given an improvement target

Study Session 9

During Study session 9 subjects will undergo endline measurements with the PRP paradigm with their assigned task orders for 12 blocks At the end of the session subjects will be debriefed and remunerated for their participation

Study Session 10

During Study session 10 subjects will undergo endline measurements with the Mixed tasks paradigm for 12 blocks At the end of the session subjects will be debriefed and remunerated for their participation

Study Session 11

During Study session 11 subjects will undergo endline measurements of the neural representations of tasks The MRI protocol will be administered with the Mixed tasks paradigm

Study Session 12

During Study session 12 subjects will undergo endline measurements of the neural representations of tasks The MRI protocol will be administered with the PRP paradigm

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
5R01MH125497 NIH None httpsreporternihgovquickSearch5R01MH125497