- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04964674
Psychometric Testing and Cue Utilization During Cued Visual Search
October 3, 2023 updated by: Lehigh University
The experimenters will examine the relationship between utilization of positive (target cue) and negative (distractor cue) templates during a cued visual search task with performance on a set of measures related to executive functions associated with attentional control: shifting, updating, and inhibition.
Study Overview
Detailed Description
The experimenters will utilize the typical procedures for the cued attentional task, while also deploying the Miyake executive function analysis.
Data will also include a working memory capacity measure.
Study Type
Interventional
Enrollment (Estimated)
99
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 Contact
- Name: Nancy B Carlisle, PhD
- Phone Number: 610-758-5122
- Email: nbc415@lehigh.edu
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Normal or corrected-to-normal visual acuity, normal color vision
Exclusion Criteria:
- age
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: Attentional Tests- Miyake and others
All participants will complete a series of behavioral tasks, including cued visual search with positive, negative, and neutral cues, Miyake executive attention tasks, and a visual working memory task.
Single Arm.
|
Take measurements of behavioral performance
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Positive, Negative, Neutral Attention Task Performance Speed
Time Frame: 1 day
|
Reaction times on visual search task with positive, negative, and neutral cues
|
1 day
|
Positive, Negative, Neutral Attention Task Performance Accuracy
Time Frame: 1 day
|
Accuracy on visual search task with positive, negative, and neutral cues
|
1 day
|
Miyake Executive Attention task- Updating
Time Frame: 1 day
|
Updating Attention
|
1 day
|
Miyake Executive Attention task-Shifting
Time Frame: 1 day
|
Shifting Attention
|
1 day
|
Miyake Executive Attention task-Inhibition
Time Frame: 1 day
|
Inhibition of attention
|
1 day
|
Working Memory Capacity
Time Frame: 1 day
|
Estimate of working memory capacity based on behavioral performance
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nancy Carlisle, PhD, Lehigh University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Miyake A, Friedman NP, Emerson MJ, Witzki AH, Howerter A, Wager TD. The unity and diversity of executive functions and their contributions to complex "Frontal Lobe" tasks: a latent variable analysis. Cogn Psychol. 2000 Aug;41(1):49-100. doi: 10.1006/cogp.1999.0734.
- Arita JT, Carlisle NB, Woodman GF. Templates for rejection: configuring attention to ignore task-irrelevant features. J Exp Psychol Hum Percept Perform. 2012 Jun;38(3):580-4. doi: 10.1037/a0027885. Epub 2012 Apr 2.
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, 2021
Primary Completion (Estimated)
March 30, 2024
Study Completion (Estimated)
March 30, 2024
Study Registration Dates
First Submitted
April 14, 2021
First Submitted That Met QC Criteria
July 6, 2021
First Posted (Actual)
July 16, 2021
Study Record Updates
Last Update Posted (Actual)
October 5, 2023
Last Update Submitted That Met QC Criteria
October 3, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1R15EY030247-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Anonymous behavioral performance data will be available for other researchers upon request
IPD Sharing Time Frame
Upon publication of the work, for at least 5 years
IPD Sharing Access Criteria
Request
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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