- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05863715
Working Memory Quality of Attentional Templates
May 16, 2023 updated by: Lehigh University
In this line of research, the researchers are examining a basic science question regarding the working memory representations underlying visual search using a positive template (looking for a target) or a negative template (avoiding a distractor).
Study Overview
Detailed Description
When finding a search target, receiving a target cue or distractor cue can increase search efficiency.
Critically, in order to use these cues to help search performance, they must be maintained in working memory.
The researchers are examining whether the working memory representations are of similar quality for a target cue (positive template) or distractor cue (negative template).
Study Type
Interventional
Enrollment (Actual)
34
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
- 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 Cue Type
Participants receive a target color cue (positive), a distractor color cue (negative), or a neutral non-informative cue prior to visual search.
|
Participants receive a target color cue (positive), a distractor color cue (negative), or a neutral non-informative cue prior to visual search.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Button Press Reaction Time
Time Frame: Day 1 (single day of 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
|
Day 1 (single day of testing)
|
|
Button Press Accuracy
Time Frame: Day 1 (single day of testing)
|
Accuracy of responses to target item-measure whether the participants presses the correct button which corresponds to the target shape presented on the computer screen or the incorrect button
|
Day 1 (single day of testing)
|
|
Working Memory Report Quality
Time Frame: Day 1 (single day of testing)
|
Accuracy of computer clicks on a set of colors to indicate memory of cue presented
|
Day 1 (single day of testing)
|
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
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)
September 27, 2022
Primary Completion (Actual)
November 17, 2022
Study Completion (Actual)
November 17, 2022
Study Registration Dates
First Submitted
May 3, 2023
First Submitted That Met QC Criteria
May 16, 2023
First Posted (Actual)
May 18, 2023
Study Record Updates
Last Update Posted (Actual)
May 18, 2023
Last Update Submitted That Met QC Criteria
May 16, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 7R15EY030247-01A1 (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
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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