Systems and methods are disclosed for assessing user physiology via eye tracking data. One method includes determining a plurality of visual assessments; determining, for each assessment of the plurality of visual assessments, a data schema, where at least one data schema is associated with more than one assessment of the plurality of visual assessments; storing the determined data schema; receiving user eye tracking data associated with a selected visual assessment of the plurality of visual assessments; determining, of the stored data schema(a), a selected stored data schema associated with the selected visual assessment; categorizing the received eye tracking data based on the selected stored data schema; computing quantitative data based on the categorized data and data related to one or more individuals other than the user; generating a report of user physiological function based on the computed quantitative data; and outputting the report to a web portal.

According to a method for determining metamorphopsia based on user interaction disclosed as an embodiment of the present invention, a test chart may be displayed to a user, an input from the user for a part which is perceived as being distorted in the displayed test chart may be received, and a metamorphopsia degree of the user may be accurately determined based on a distortion area selected according to the received input. Further, according to another embodiment of the present invention, a test chart may be displayed to a user, a response (e.g., distance values of points, an area value, etc. in a zone) for each zone for the test chart may be received from the user, and metamorphopsia of the user may be determined based on the received response.

An OCT system for generating images of an anterior or posterior segment of an eye is described. The system includes a light source, a controller, optics, a detector, and a processor. The light source generates a beam of light and is capable of operating in a posterior or an anterior segment imaging mode. In the posterior segment imaging mode, the light source outputs light with a spectral bandwidth equal or narrower than the width of the 1060 nm water absorption window. In the anterior segment imaging mode, the light source outputs light with a spectral bandwidth larger than the width of the 1060 nm water absorption window. The controller enables switching between the posterior or anterior segment imaging mode. The optics scan the light over a set of transverse locations across the eye. The detector measures returning light and generates output signals for use by the processor to generate images.

The invention relates to a system and to a method for training head movements of a person. Visual stimuli are generated with a visual stimulus generation device for a left and/or right eye of the person. Head movements of the person are captured with a measurement device. The head movement of the person captured with respect to a generated visual stimulus is assessed in a computational unit. Assessment information that is dependent on the assessment of the head movement captured with respect to a generated visual stimulus is then provided for the person with an output device.

Systems and methods are disclosed for assessing user physiology via eye tracking data. One method includes determining a plurality of visual assessments; determining, for each assessment of the plurality of visual assessments, a data schema, where at least one data schema is associated with more than one assessment of the plurality of visual assessments; storing the determined data schema; receiving user eye tracking data associated with a selected visual assessment of the plurality of visual assessments; determining, of the stored data schema (a), a selected stored data schema associated with the selected visual assessment; categorizing the received eye tracking data based on the selected stored data schema; computing quantitative data based on the categorized data and data related to one or more individuals other than the user; generating a report of user physiological function based on the computed quantitative data; and outputting the report to a web portal.

An intraocular pressure sensor is presented that achieve very low power consumption. The intraocular pressure sensor takes the form of an implantable assembly configured to be implanted in an eye of a subject. Specifically, the implantable assembly is comprised of a capsular tension ring attached to a flexible printed circuit board. The flexible printed circuit board includes a cutout that is sized to encircle the pupil of the eye and is C shaped. One or more electrical components are also mounted onto the flexible printed circuit board. One such component is a voltage reference generator that is implemented by a circuit which provides inherently low process variation and low power consumption.

Various embodiments of an eye imaging apparatus are disclosed. In some embodiments, the eye imaging apparatus may comprise a light source, an image sensor, a hand-held computing device, and an adaptation module. The adaptation module comprises a microcontroller and a signal processing unit configured to adapt the hand-held computing device to control the light source and the image sensor. In some embodiments, the imaging apparatus may comprise an exterior imaging module to image an anterior segment of the eye and/or a front imaging module to image a posterior segment of the eye. The eye imaging apparatus may be used in an eye imaging medical system. The images of the eye may be captured by the eye imaging apparatus, transferred to an image computing module, stored in an image storage module, and displayed in an image review module.

An eye-fatigue examining device and an eye-fatigue examining method capable of examining eye fatigue of a subject's eye regardless of an age of a patient are provided. The eye-fatigue examining device includes: a light quantity difference adjusting unit that increases a light quantity difference between lights respectively incident on right and left subject's eyes; a gaze direction detecting unit that detects gaze directions of the respective subject's eyes while the light quantity difference adjusting unit increases the light quantity difference; and a light quantity difference deciding unit that decides a specific light quantity difference at which a change in the gaze directions due to the increase in the light quantity difference occurs, based on the detection result of the gaze direction detecting unit.

An ultra wide field fundus imaging system comprises a photosource, an optical splitter, a scanning assembly, a curved reflector, a probe pinhole and an imaging assembly. The scanning assembly includes a first scanning mirror scanning along a first direction and a second scanning mirror scanning along a second direction. The light emitted by the photosource passes through the optical splitter, then successively is reflected by the first scanning mirror, the curved reflector, the second scanning mirror and the curved reflector, and then enters in the fundus; the light entering the fundus is reflected by the retina and then successively is reflected by the curved reflector, the second scanning mirror, the curved reflector, the first scanning mirror and then returned to the optical splitter; the light is reflected by the optical splitter and passes through the probe pinhole, finally the light enters in the imaging assembly. Compared with the prior art, the ultra wide field fundus imaging system realizes fundus imaging by total reflection and can effectively avoid ghost images caused by lens module imaging to improve the imaging quality. Since the curvature of the curved reflector is gradually changed, so the light reflected by the curved reflector can enter in the fundus at a larger incident angle to achieve wide field imaging.

The methods and systems provided can automatically determine an Arteriolar-to-Venular diameter Ratio, AVR, in blood vessels, such as retinal blood vessels and other blood vessels in vertebrates. The AVR is an important predictor of increases in the risk for stroke, cerebral atrophy, cognitive decline, and myocardial infarct.