Task Switching Between Target Templates During Visual Search in Healthy Adults

October 7, 2024 updated by: Lehigh University

Task Switching Between Positive and Negative Target Templates During Visual Search in Healthy Adults

In this line of research, the researchers having participants engage in task switching between tasks which require a positive (target) template, negative (distractor) template, or neutral (non-informative) template to the cognitive control factors associated with each template type during visual search. This is a basic science study.

Study Overview

Status

Enrolling by invitation

Conditions

Intervention / Treatment

Detailed Description

The researchers will have participants engage in task switching between tasks which require a positive (target) template, negative (distractor) template, or neutral (non-informative) template to the cognitive control factors associated with each template type during visual search. Looking for impacts of task switching helps to identify the components of the cognitive control system that overlap between different types of attentional templates. This is a basic science study.

Study Type

Interventional

Enrollment (Estimated)

24

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

  • United States
    • 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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

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

Exclusion Criteria:

-

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
Behavioral: Experimental: Within-Subjects Attentional Information
Behavioral: Visual Search Information Type (target or distractor information) Participants will have information about targets, distractors, or neither in different trials of the intervention.
Other Names:
  • Within-Subjects, all participants receive all interventions

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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)
Eye Movements to Objects on Computer Screen
Time Frame: One day (during testing)
Proportion (% of total) of eye movements directed to potential targets or distractors, measured with an Eye Link II eye tracker
One day (during testing)

Collaborators and Investigators

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

Sponsor

Lehigh University

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)

April 12, 2023

Primary Completion (Estimated)

February 17, 2025

Study Completion (Estimated)

June 17, 2025

Study Registration Dates

First Submitted

January 24, 2023

First Submitted That Met QC Criteria

January 24, 2023

First Posted (Actual)

February 2, 2023

Study Record Updates

Last Update Posted (Estimated)

October 9, 2024

Last Update Submitted That Met QC Criteria

October 7, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 4R15EY030247-01A1 (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.

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