Dark adaptation measurement with a mobile device
Dark adaptation measurement with a mobile device
批准号:
10006831
负责人:
SHRINIVAS PUNDLIK
金额:
$23.82万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-30 至 2022-08-31
关键词:
AdoptedAdoptionAffectAgeAge FactorsAge related macular degenerationAgreementAlgorithmsAnalysis of VarianceBiological MarkersBlindnessCellular PhoneCharacteristicsClinicClinicalComputer softwareCustomDark AdaptationDarknessDataDetectionDevicesDiseaseDisease ProgressionEarly DiagnosisElderlyElectronicsEnvironmentEvaluationExposure toEyeFaceGoalsHealthHealth Services AccessibilityHome environmentImpairmentImprove AccessIndividualLeadLightLightingMeasurementMeasuresMethodsMonitorOutcomeParticipantPatientsPhotoreceptorsPopulationPopulations at RiskProceduresProcessReadingRegression AnalysisRetinaRiskScreening procedureSensitivity and SpecificitySeriesSeveritiesStimulusStructureTest ResultTestingTimeValidationVisionVision DisordersVisual AcuityWorkbasecostcost effectiveeffectiveness evaluationhandheld mobile deviceimage processinginstrumentluminancenovelresponsesample fixationscreeningvirtual realityvirtual reality headsetvisual stimulus
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英文摘要
Project Summary / Abstract
In this project we propose to validate a mobile device based dark adaptation measurement method for
detection of age-related macular degeneration (AMD). Dark adaptation (DA) is the natural process where our
eyes adapt to darkness after being exposed to a bright light. This process of DA is known to be impaired or
delayed in people with AMD, even at a very early stage when other vision measures such as visual acuity (VA)
are unaltered. Delays in dark adaptation are also correlated with severity of AMD. Thus, DA is a key biomarker
of AMD which can be helpful in early detection and even monitoring disease progression. While dedicated
clinical devices for DA measurement have been developed, their high cost and limited availability are barriers
for adoption of DA testing as part of screening tests for AMD. If a key vision measurement like dark adaptation
can be adopted on a consumer electronics platform such as mobile devices, it can be made accessible to a
large at-risk population in a cost-effective manner. We have developed a method for mobile device based DA
measurement (MOBILE-DA). Subjects sitting in a dark room fixate on a target on the mobile device placed at
reading distance, and a series of visual stimuli are presented at a fixed eccentricity with respect to the fixation.
The subjects respond to the perceived stimulus by tapping the screen and the device logs the data. Preliminary
experimentation suggests that it is feasible to measure DA using contemporary mobile devices. The DA
response measured using MOBILE-DA differed significantly between AMD subjects and elderly normal
controls, indicating that MOBILE-DA could be sensitive to measuring functional vision changes occurring in
AMD. In this project, our main aim is to evaluate the effectiveness of MOBILE-DA in measuring DA
characteristics in early/intermediate stage AMD patients with visual acuity 20/40 or better. A significant
association of AMD presence on MOBILE-DA characteristics will imply that MOBILE-DA can be potentially
used as an early detection tests in clinic. We will compare MOBILE-DA measurements with an existing clinical
dark adaptometer device in all study participants for its further validation. We will also compare MOBILE-DA
measurements between early and intermediate AMD subject groups to determine whether MOBILE-Da
parameters are significantly associated with the severity of AMD. This will impact its potential to be used for
monitoring disease progression. The second aim of this project is to develop a custom smartphone virtual
reality (VR) googles for deploying MOBILE-DA to obtain better control over measurement conditions by
reducing the interference of external lighting conditions and for allowing automated monitoring of fixation
stability during the test using the front camera of the smartphones and novel image processing algorithms. We
will compare within-subjects the MOBILE-DA measurements with and without smartphone VR googles mode.
This study will help us comprehensively evaluate different aspects of MOBILE-DA and its potential to impact
AMD screening in the short-term, home-monitoring in AMD patients by enabling self-testing in the long term.
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