SSVEP and Distractor Processing During Visual Search

September 26, 2024 updated by: Lehigh University

SSVEP and Distractor Processing During Visual Search in Healthy Adults

In this line of research, the researchers are utilizing an EEG measure of repeated visual stimulation, the Steady-State Visually Evoked Potential (SSVEP) to examine processing of target and distractor information during visual search. This is a basic science study.

Study Overview

Status

Enrolling by invitation

Conditions

Detailed Description

The researchers are interested in how the brain responds to target and distractor information during visual search. The researchers will manipulate the information available to the research participants, and measure research participants brain responses to information matching target or distractor features utilizing an EEG measure of repeated visual stimulation, the Steady-State Visually Evoked Potential (SSVEP).

Study Type

Interventional

Enrollment (Estimated)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Bethlehem, Pennsylvania, United States, 18015
        • Lehigh University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • normal or corrected to normal visual acuity, normal color vision

Exclusion Criteria:

  • history of neurological disorders

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Within-Subjects Attentional Information
Within-Subjects, all participants receive all interventions
Participants will have information about targets, distractors, or neither in different blocks of the intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Steady-State Visually Evoked Response (SSVEP)
Time Frame: One day (during testing)
Brain response to visual stimuli flashing at a pre-defined frequency
One day (during testing)
Button Press Reaction Time
Time Frame: One day (during testing)
Speed to respond correctly to the target- after participant finds the target shape on a computer screen, they press a button to indicate what shape they see
One day (during testing)
Button Press Accuracy
Time Frame: One day (during testing)
Accuracy of responses to target item (% correct)- the researchers will measure whether the participants presses the correct button which corresponds to the target shape presented on the computer screen or the incorrect button
One day (during testing)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nancy Carlisle, PhD, Lehigh University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 15, 2021

Primary Completion (Estimated)

November 15, 2024

Study Completion (Estimated)

May 15, 2025

Study Registration Dates

First Submitted

November 7, 2022

First Submitted That Met QC Criteria

November 28, 2022

First Posted (Actual)

December 1, 2022

Study Record Updates

Last Update Posted (Actual)

September 27, 2024

Last Update Submitted That Met QC Criteria

September 26, 2024

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 3R15EY030247-01A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The researchers plan to share anonymized subject data on Open Science Framework.

IPD Sharing Time Frame

Upon publication.

IPD Sharing Access Criteria

Open Science Framework internet access.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Healthy

Clinical Trials on Visual Search Information Type (target or distractor information)

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