NCT06673303

Brief Summary

A fundamental problem in neuroscience is how the brain computes with noisy neurons. An advantage of population codes is that downstream neurons can pool across multiple neurons to reduce the impact of noise. However, this benefit depends on the noise associated with each neuron being independent. Noise correlations refer to the covariance of noise between pairs of neurons, and such correlations can limit the advantages gained from pooling across large neural populations. Indeed, a large body of theoretical work argues that positive noise correlations between similarly tuned neurons reduce the representational capacity of neural populations and are thus detrimental to neural computation. Despite this apparent disadvantage, such noise correlations are observed across many different brain regions, persist even in well-trained subjects, and are dynamically altered in complex tasks. The investigators have advanced the hypothesis that noise correlations may be a neural mechanism for reducing the dimensionality of learning problems. The viability of this hypothesis has been demonstrated in neural network simulations where noise correlations, when embedded in populations with fixed signal-to-noise ratio, enhance the speed and robustness of learning. Here the investigators aim to empirically test this hypothesis, using a combination of computational modeling, fMRI and pupillometry. Establishing a link between noise correlations and learning would open the door to an investigation into how brains navigate a tradeoff between representational capacity and the speed of learning.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
47

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 18, 2024

Completed
17 days until next milestone

First Posted

Study publicly available on registry

November 4, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

December 14, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2025

Completed
Last Updated

May 26, 2026

Status Verified

November 1, 2024

Enrollment Period

9 months

First QC Date

October 18, 2024

Last Update Submit

May 21, 2026

Conditions

Keywords

noise correlationsperceptual learningneural networkfeature dimensions

Outcome Measures

Primary Outcomes (2)

  • Participant learning asymmetry in the behavioral task

    The participants' learning asymmetries on the task-relevant and task-irrelevant dimensions are evaluated with our reinforcement learning model that recover their learning gradient on the respective learning dimensions.

    From the end of the behavioral session to the beginning of the scanning session, typically within a week

  • Noise correlations in the brain

    The investigators will identify the noise correlation - the ratio of trial-by-trial variability associated with a stimulus along the task-relevant versus task-irrelevant coding axes. The coding axes will be decoded from region of interests using multi-voxel patterns associate with individual trials.

    Through completion of analysis, an average of 6 months

Study Arms (1)

Dynamic perceptual discrimination task

EXPERIMENTAL

The task featured two task conditions, each of which required the integration of information from both stimulus dimensions. In each condition, participants viewed a stimulus containing motion and color information and were required to specify one of two possible responses. Within each condition, rules and the response mapping changed occasionally, but always by changing on a fixed feature dimension (ie. rightward/purple, leftward/orange). These uncued intra-dimensional shifts involved translational shifts in the learning boundary, requiring them to adapt their decision making within a familiar dimension. These shifts compelled participants to continuously adjust their learning strategies by focusing on the most relevant feature dimension.

Behavioral: Dynamic perceptual discrimination taskDiagnostic Test: fMRI

Interventions

The study featured two task conditions, each of which required the integration of information from both stimulus dimensions. In each condition, participants viewed a stimulus containing motion and color information and were required to specify one of two possible responses. Within each condition, rules and the response mapping changed occasionally, but always by changing on a fixed feature dimension (ie. rightward/purple, leftward/orange). These uncued intra-dimensional shifts involved translational shifts in the learning boundary, requiring them to adapt their decision making within a familiar dimension. These shifts compelled participants to continuously adjust their learning strategies by focusing on the most relevant feature dimension.

Dynamic perceptual discrimination task
fMRIDIAGNOSTIC_TEST

Participant brain imaging data will be collected concurrently while performing the perceptual discrimination task.

Dynamic perceptual discrimination task

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age above 18
  • Normal or correctable vision

You may not qualify if:

  • Age under 18
  • Claustrophobia
  • Color blindness
  • Neuroleptics medications
  • History of drug abuse and/or alcoholism
  • Conditions contraindicated for MRI such as:
  • Surgical implant that is not MRI compatible
  • Metal fragments in the body
  • Tattoo with metallic ink
  • Eye diseases / impairment:
  • Cataracts
  • Macular degeneration
  • Retinopathies
  • Partial vision loss
  • Medical history:
  • +5 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Brown University

Providence, Rhode Island, 02906, United States

Location

Related Publications (3)

  • Fusi S, Miller EK, Rigotti M. Why neurons mix: high dimensionality for higher cognition. Curr Opin Neurobiol. 2016 Apr;37:66-74. doi: 10.1016/j.conb.2016.01.010. Epub 2016 Feb 4.

    PMID: 26851755BACKGROUND
  • Cohen MR, Newsome WT. Context-dependent changes in functional circuitry in visual area MT. Neuron. 2008 Oct 9;60(1):162-73. doi: 10.1016/j.neuron.2008.08.007.

    PMID: 18940596BACKGROUND
  • Nassar MR, Scott D, Bhandari A. Noise Correlations for Faster and More Robust Learning. J Neurosci. 2021 Aug 4;41(31):6740-6752. doi: 10.1523/JNEUROSCI.3045-20.2021. Epub 2021 Jun 30.

    PMID: 34193556BACKGROUND

MeSH Terms

Interventions

Magnetic Resonance Imaging

Intervention Hierarchy (Ancestors)

TomographyDiagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Study Officials

  • Matthew Nassar, PhD

    Brown University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 18, 2024

First Posted

November 4, 2024

Study Start

December 14, 2024

Primary Completion

September 1, 2025

Study Completion

September 1, 2025

Last Updated

May 26, 2026

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Anyone interested in IPD should reach out to the Principal Investigator

Locations