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NIH/NIBIB EB007163
PI: Carlo J. De Luca, PhD1 Co-PIs: Serge H. Roy, ScD1, S. Hamid Nawab, PhD1,2, Joe Jabre, MD3 Other Key Persons: L. Gilmore, ABEE1, Samuel Chang, MS1,2, Peter Novak, MD3, Cathi Thomas, RN, MS3
2
BOSTON
UNIVERSITY
NeuroMuscular Research Center, Boston University Electrical and Computer Engineering, College of Engineering, Boston University 3 Department of Neurology, Boston Medical Center
1
Medicine
SCHOOL of
Goal:
To develop a Personal Status Monitor (PSM) that automatically identifies and tracks movement disorders, medication states, and mobility in patients with Parkinsons disease. Project 2: Clinical Application to PD
Data Collection Protocol: patients are monitored using the Personal Status Monitor (PSM) and are videotaped during
this approximately 4-hour period that is timed to coincide with a complete medication cycle (from On to wearing Off). Activities are conducted in a laboratory configured like an apartment. The activities include standardized motor tests used for clinical assessment (e.g. motor scales from UPDRS), scripted functionl tasks (e.g. sit-stand-and-walk) and freeroaming activity.
Movement Disorders
W earable Wireless ireless E M GM S ystem W earable W E G S ystem
with Parkinsons disease. Physicians rely on patient diaries to monitor these complications. Diaries need to be recorded every 15 min, are often inaccurate, have poor time resolution, and are difficult for patients to manage.
Proposed Solution
Medication States
Levodopa Intake Onset Dyskinesia Peak-Dose Dyskinesia End-of-Dose Dyskinesia
Mobility States Sitting Standing Walking Lying Down The PSM will automatically identify transitions between these four mobility states.
Tremor: Oscillatory, rhythmic movement Bradykinesia: Slow movement Akinesia: Inability to initiate a movement Dyskinesia: Spasmodic movement ment t h a
OFF
Off-Period Freezing disorders Bradykinesia t Tremor
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Off-Period Freezing Bradykinesia Tremor
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WEARING-OFF
Hardware developed by research team members to acquire and store multi-channel signals from hybrid sensors using wireless technology. Hybrid sensors under development in this project will detect EMG and accelerometer (ACC) signals.
The PSM will automatically identify these four different movement disorders associated with Parkinsons disease and their severity.
The PSM will automatically identify the onset and duration of the patients On, Off, and On-with-Dyskinesia medication phases.
Walking While On
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A schematic of the proposed Personal Status Monitor (PSM) for identifying movement disorders, medication states, and mobility in patients with Parkinsons disease by the automatic analysis and interpretation of electromyographic (EMG) and accelerometer (ACC) signals recorded from the surface of the body. In this example, the PSM device is monitoring the subject while walking. The proposed system will provide a continuous history and statistical summarization that can be made available to the clinician to help manage
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Algorithm Development
Planner
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T ime (s )
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Knowledge Sources
Assessment level C E D Abnormality level F E D C B A Mobility Epoch. Abnorm. Mobility Assess. Abnorm. Abnorm. Assess. Mobility Abnorm. Epoch Mobility
Raw data
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Feature Extraction
Filter
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Sample data from a patient asked to sit quietly and not move. The figure on the left was taken during his Off period when he was experiencing Tremor and on the right during his On w/ Dyskinesia period. Data were recorded from the Anterior Deltoid (Ch1-4) and Biceps brachii (Ch 5-8). EMG signals are in black; ACC signals are in blue.
-1
Sample data from the same patient while walking. The figure on the left was taken during his On period when he walked normally without movement disorders and on the right during his Off period when he had Akinesia or Freezing. Data were recorded from the Quadraceps (Ch1-4) and Tibialis Anterior muscles (Ch 5-8).
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Preliminary Results
Results from the algorithms provide automatic classification of mobility states and movement disorders in a patient with PD transitioning from Off to On-with-Dyskinesia. Classification is made solely on the basis of EMG and ACC data. Only 4 of the 8 sensors were used for the mobility analysis. No attempts were made to reduce the number of requisite sensors (to less than 8) for identifying movement disorders at this stage of algorithm development. Classification resolution is 1s and the sensitivity is 95% based on the interpretation of videotaped data by movement disorder specialists. The patient is a 73 y.o. male with advanced PD characterized by severe motor fluctuations.
Filter
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Output Layer
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DATA Acquisition
Blackboard Database
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Walking
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Blackboard architecture for the PSM application. The blackboard database shown here contains four data representation levels (Signal Epoch, Mobility, Movement Abnormality, and Medication State). Transformations between levels are carried out by a collection of independent programs that are typically called Knowledge Sources and are invoked according to algorithmically defined control plans.
Features from the raw EMG and ACC signals are analyzed using Artificial Neural Networks (ANNs). More specifically, dynamically evolving features for each activity are characterized through TimeDependent Neural Networks. ANN technology is being used in conjunction with Rule-Based Systems technology. Iterative Correlation Analysis is used for correcting initial identifications. These diverse techniques operate collectively through the Blackboard architecture in the previous figure.
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Bradykinesia
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Dyskinesia
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P A
Tremor
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We have built a custom hybrid surface sensor acquisition system for acquiring EMG and ACC signals from patients and control subjects. Algorithm development has been enhanced for standardized and singular activities using a blackboard-based signal processing system and time-dependent neural networks. Preliminary classification results for patients with Parkinson's disease resulted in 95% sensitivity for mobility and movement disorders during standardized and singular activities. We are currently preparing to acquire sufficient data to enhance the algorithms for monitoring patients during unconstrained free-form activities.
Special thanks to the patients and staff of the Boston University Parkinsons Disease Center