Eye Movements, Visual Perception and Attention
2 other identifiers
interventional
155
1 country
1
Brief Summary
During visual fixation, small eye movements of which we are usually not aware, prevent the maintenance of a steady direction of gaze. These eye movements are finely controlled and shift retinal projection of objects within the fovea, the region of the retina where visual acuity is highest. This program of research examines the link between these eye movements and attention, and tests the hypothesis that attention, similarly to eye movements, can be controlled at the foveal level. Psychophysical experiments with human subjects, using state-of-the-art techniques, high resolution eyetracking and retinal stabilization are conducted to address these questions. Gaze-contingent calibration procedures are employed to achieve high accuracy in gaze localization. A custom developed gaze-contingent display is used to shift in real-time visual stimuli on the monitor to compensate for the observer eye movements during fixation periods and to maintain stimuli at a desired location on the retina. Experiments involve visual discrimination/detection tasks with stimuli presented at selected eccentricities within the fovea. Participants' performance and reaction times are examined under different conditions, in which various types of attention are manipulated. In addition to advancing our basic understanding of visual perception, this research leads to a better understanding of attentional control at the foveal scale and of the contribution of microscopic eye movements to the acquisition and processing of visual details.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedFirst Submitted
Initial submission to the registry
March 20, 2019
CompletedFirst Posted
Study publicly available on registry
March 21, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2024
CompletedResults Posted
Study results publicly available
June 18, 2025
CompletedJune 18, 2025
June 1, 2025
6.1 years
March 20, 2019
May 15, 2025
June 3, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
Average Performance in Visual Tasks
Proportion correct responses in visual tasks. For each visual stimulus presentation, observers performed a four-alternative forced-choice (4AFC) task. A trial was considered correct if the participant's selected response matched the identity of the presented stimulus; otherwise, it was marked as incorrect.
Day 0
Microsaccades Rate
rate of microsaccades per second
Day 0
Study Arms (1)
Normal Vision
EXPERIMENTALThis study examines high-acuity vision, oculomotor behavior recorded using high-resolution eyetracking. Healthy participants are asked to perform different types of visual tasks, ranging from letter identification to judging facial expressions while their eye movements will be recorded with high-precision together with their behavioral performance in the task.
Interventions
In the experiments, participants will sit in front of a computer monitor located a less than a meter of distance and will analyze the content of images extracted from collections of natural and computer-generated scenes. Subjects will be asked to report verbally or by pressing keys on a keyboard on image characteristics such as the locations of the objects present in the scenes, their number and/or their identities. Some experiments will involve a search paradigm in which subjects will have to report on the location and/or fine characteristics of a target element among a field of distracting similar elements, and/or visual discrimination tasks. The duration of the interval of time in which the image is maintained on the screen may be varied between few tens of milliseconds to several seconds. In a set of experiments, the eye movements performed by the subjects during the execution of the visual tasks will be recorded as explained below.
Eligibility Criteria
You may qualify if:
- Subjects will be eligible for the study if they:
- Are at least 18 years old
- Speak English
- Have read, understood, and signed the informed consent form Have normal visual acuity (20/20 or better) without correction (i.e. without glasses or contact lenses) and no known visual deficits. A standard visual acuity screening will be performed by means of a Snellen chart (the standard eye chart) at the beginning and the end of the experiments.
You may not qualify if:
- Subjects will be excluded if they:
- Are under 18 years old
- Cannot understand the experimental procedures Have reported vision loss, including the need for correction (i.e. glasses or contact lenses), or fail the visual acuity screening performed during the experiments. We expect a very minor portion of subjects to be excluded as a result of this test, as the good vision requirement will be clearly stated in our recruitment materials. There will be no data collection for subjects who will not pass the acuity test.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Rochesterlead
- National Eye Institute (NEI)collaborator
Study Sites (1)
University of Rochester
Rochester, New York, 14642, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Martina Poletti
- Organization
- University of Rochester
Study Officials
- PRINCIPAL INVESTIGATOR
Martina Poletti, Ph.D.
University of Rochester
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 20, 2019
First Posted
March 21, 2019
Study Start
January 1, 2018
Primary Completion
February 1, 2024
Study Completion
February 1, 2024
Last Updated
June 18, 2025
Results First Posted
June 18, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share