- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05633238
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
Intervention / Treatment
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.
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)
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
Keywords
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.
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