DiSCERN: Advanced PD Therapy Candidacy and Evaluation System
DiSCERN: Advanced PD Therapy Candidacy and Evaluation System
批准号:
10207343
负责人:
Aaron John Hadley
金额:
$80.27万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-20 至 2024-06-30
关键词:
Academic Medical CentersActivities of Daily LivingAlgorithmsAwarenessCaringCellular PhoneCessation of lifeChronicClinicClinicalClinical assessmentsCollectionCommunitiesComputer softwareDataData CollectionDecision MakingDeep Brain StimulationDetectionDevelopmentDiagnosisDisadvantagedDoseDyskinetic syndromeEmotionalEvaluationExpert SystemsFatigueFeedbackHealthHealth Care CostsHealth TechnologyHealthcareHomeImpaired cognitionImplantIncidenceInstitutionLeadLettersLevodopaMeasuresMedicalMethodsModelingMonitorMotorMovement DisordersNeurologyOperative Surgical ProceduresOutcomeParkinson DiseasePatient SelectionPatientsPerceptionPharmaceutical PreparationsPhasePilot ProjectsPopulationProcessProviderPumpQuality of lifeQuestionnairesResourcesRiskRuralRural PopulationScreening procedureSelection BiasSelf AssessmentSensitivity and SpecificitySiteSpecialistStandardizationSymptomsSystemTechnologyTelemedicineTherapeuticUnnecessary SurgeryValidationWireless Technologybasecompliance behaviorcostdata exchangedesigndiagnostic platformdiariesdisparity reductionexhaustexperiencehealth care deliveryhealth disparityimprovedinnovationmHealthmedical specialtiesmobile applicationmotion sensormotor disordermotor symptomnew technologynovelpatient screeningpredictive modelingpreventproduct developmentracial minorityremote monitoringremote screeningresponsescreeningside effectsmartphone Applicationsocioeconomicssuccesstherapy outcometoolwearable devicewearable sensor technology
中文摘要
总结
英文摘要
Summary
The objective is to design, develop, and clinically assess DiSCERN, a standardized telemedicine tool for
identifying patients with Parkinson’s disease (PD) who would benefit from advanced therapies (AT) and
determining when AT recipients need therapy adjustments. Once chronic PD medication usage results in
motor fluctuations and dyskinesias and all non-invasive therapies have been exhausted, AT (e.g., deep brain
stimulation, drug pumps) is often recommended. While experts at academic medical centers may appropriately
identify AT candidates, AT is underutilized due to limited access and inequitable utilization of limited evaluative
resources for a sizable subset of the PD population. Remote screening and monitoring with DiSCERN will
improve patient selection, reduce disparities, and expand access for rural populations and disadvantaged
communities. The system will engage and empower patients, providers, and healthcare institutions and lead to
improved health, healthcare delivery, and the reduction of health disparities. This mobile health technology will
include a patient friendly smartphone app, non-motor assessments, and wireless wearable sensors for
continuously monitoring PD motor symptoms, complications, and quality of life (QoL). We have previously
commercialized wearables and mobile apps for remote monitoring of PD motor symptoms and side effects,
which will significantly de-risk the project. Still, novel development and validation efforts are required to
commercialize this new technology. Innovations include: 1) integration of PD monitoring algorithms with
context aware activity detection for improved PD motor assessment and QoL quantification; 2) implementation
of the algorithms on a smartphone and wearable device; 3) development of a predictive model that uses motor
and non-motor features to accurately identify PD patients who would be good candidates for AT; and 4)
implementation of a model that alerts clinicians when an AT recipient needs a therapy adjustment. Through
integration with AT systems, DiSCERN will improve the clinician experience and allow the limited availability of
specialists to scale care to a diverse and growing PD population, who may not otherwise have access to AT.
Phase I includes: 1) validation of context aware activity detection algorithms on PD patient data; 2) determining
the extent specific activities or activity levels correlate with PD QoL; 3) using clinician feedback to identify
collected data features that are useful in informing AT clinical decisions; and 4) identification of wearables to be
used in the final system. Phase II includes: 1) transition of context aware activity detection and PD symptom
quantification algorithms onto a smartphone and wearable chips; 2) development of a smartphone app that
integrates data collection, non-motor assessment, and data-transfer to the cloud; and 3) collecting data from
AT candidates in the months before and after AT is initiated to develop models that accurately identify AT
candidates and when AT adjustments are needed. DiSCERN will improve therapy efficiency, expand access,
and result in more patients opting for AT.
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