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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05709743
Other study ID # 4R15EY030247-01A1
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date April 12, 2023
Est. completion date October 17, 2023

Study information

Verified date June 2023
Source Lehigh University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 24
Est. completion date October 17, 2023
Est. primary completion date September 17, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - normal or corrected to normal visual acuity, normal color vision Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

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.

Locations

Country Name City State
United States Lehigh University Bethlehem Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Lehigh University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Button Press Reaction Time 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)
Primary Button Press Accuracy 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)
Primary Eye Movements to Objects on Computer Screen Proportion (% of total) of eye movements directed to potential targets or distractors, measured with an Eye Link II eye tracker One day (during testing)
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