- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05784233
Relevance and Salience During Attention Task
February 1, 2024 updated by: Lehigh University
In this line of research, the researchers are examining the influence of relevance of a salient item on task performance, depending on overall task set.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
When finding a target item during visual search (looking for a pencil), a salient item can capture attention (your phone flashing from a message).
Typical attention studies only examine salient items when shown as distractor during search, to ensure any attention to the items are driven by salience alone.
However, the impact of salience may interact with the relevance of the item for the search task (e.g.
how likely the salient item is to be the target).
Here, the researchers investigate these interactions in a basic science study when participants perform an easy task or a difficult search task.
Study Type
Interventional
Enrollment (Actual)
117
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 99 years (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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 0% Relevance
0% chance of the salient item being the target during visual search task.
|
The proportion of trials, when the salient visual item is present in the array, where the salient item is the search target.
|
|
Experimental: 25% Relevance
25% chance of the salient item being the target during visual search task.
|
The proportion of trials, when the salient visual item is present in the array, where the salient item is the search target.
|
|
Experimental: 50% Relevance
50% chance of the salient item being the target during visual search task.
|
The proportion of trials, when the salient visual item is present in the array, where the salient item is the search target.
|
|
Experimental: 75% Relevance
75% chance of the salient item being the target during visual search task.
|
The proportion of trials, when the salient visual item is present in the array, where the salient item is the search target.
|
|
Experimental: 100% Relevance
100% chance of the salient item being the target during visual search task.
|
The proportion of trials, when the salient visual item is present in the array, where the salient item is the search target.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Button Press Reaction Time
Time Frame: During Testing (single day)
|
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
|
During Testing (single day)
|
|
Button Press Accuracy
Time Frame: During Testing (single day)
|
Accuracy of responses to target item- 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
|
During Testing (single day)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 15, 2022
Primary Completion (Actual)
October 28, 2022
Study Completion (Actual)
October 28, 2022
Study Registration Dates
First Submitted
March 13, 2023
First Submitted That Met QC Criteria
March 13, 2023
First Posted (Actual)
March 24, 2023
Study Record Updates
Last Update Posted (Estimated)
February 2, 2024
Last Update Submitted That Met QC Criteria
February 1, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 5R15EY030247-01A1 (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
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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