The purpose of the research is to better understand the motor behavior of individuals in health and disease. The specific purpose of this project is to identify if we can utilize a smartphone to diagnose different movement disorders and monitor their symptoms. A. Objectives 1. Estimate symptom severity of Essential tremor (ET), Parkinson's disease (PD), Huntington's disease (HD), Primary focal dystonia (PFD), spinocerebellar ataxia (SCA), and Functional movement disorders (FMD) using a smartphone-based application 2. Differentiate individuals with the different movement disorders from healthy controls based on features from the smartphone data 3. Differentiate individuals with a specific movement disorder from people with other movement disorders based on features from the smartphone data B. Hypotheses / Research Question(s) We hypothesize that we can estimate the severity of symptoms using a smartphone application and that, using those estimates, we can differentiate individuals with movement disorders from healthy controls and from people with other movement disorders.
Movement disorders are a group of neurological conditions that alter human movements. They lead to functional impairments, diminished quality of life, and significant societal, economic, and familial burden. Due to the increase in population and longer life expectancy \[1\], more and more people will have to live with movement disorders. However, access to movement disorder specialists is already limited and will get worse \[2\]. Therefore, there is an urgent need to develop tools to aid non-specialist medical professionals identify and manage the symptoms (both motor and non-motor) of those disorders such that specialist can focus on more severe and complex cases. While there are several conditions that can be classified as movement disorders, the current proposal will focus on six disorders that have overlapping symptoms and could prove difficult to differentiate for non-specialists and/or clinicians that do not readily have access to genetic testing or imaging facilities: Essential tremor (ET), Parkinson's disease (PD), Huntington's disease (HD), primary focal dystonia (PFD), spinocerebellar ataxia (SCA), and functional movement disorders (FMD). While trained movement disorder specialists may correctly identify each of these disorders and provide optimal treatment, general practitioners and clinicians living in rural areas that do not have access to the most up-to-date diagnostic tools, such as neuroimaging and genetic testing, may face difficulty when treating those patients due to symptom variability and overlap in symptom presentation between different disorders; leading to sub-optimal treatment outcomes. As such, the development of simple, accurate, and inexpensive tools to help guide their clinical decisions is warranted. The ubiquity of mobile technology and wearable sensors may enable the development of such a tool. In recent years, our group and others have used mobile phones and wearable technology to assess symptoms in a multitude of disorders. This highlights the feasibility of our proposed system for the assessment and monitoring of symptom severity in individuals with movement disorders.
Study Type
OBSERVATIONAL
Enrollment
210
Rutgers University
Newark, New Jersey, United States
RECRUITINGUPDRS-III (Unified Parkinson's Disease Rating Scale)
1. Speech (rating 0-4 were 0 is normal and 4 is Unintelligible), similarly following activities are recorded with a scale of (0-4) 2. Facial Expression 3. Tremor at Rest (head, upper and lower extremities) 4. Action or Postural Tremor of Hands 5. Rigidity (Judged on passive movement of major joints with patient relaxed in sitting position. Cogwheeling to be ignored.) 6. Finger Taps (Patient taps thumb with index finger in rapid succession.) 7. Hand Movements (Patient opens and closes hands in rapid succession) 8. Rapid Alternating Movements of Hands (Pronation-supination movements of hands, vertically and horizontally, with as large an amplitude as possible, both hands simultaneously.) 9. Leg Agility (Patient taps heel on the ground in rapid succession picking up entire leg. Amplitude should be at least 3 inches.) 10. Arising from Chair 11. Posture 12. Gait 13. Postural Stability 14. Body Bradykinesia and Hypokinesia
Time frame: Will occur right after the consent received from patients during the first lab visit.
TETRAS-performance (The Essential Tremor Rating Assessment Scale)
Head Face Tongue Voice Upper limb Lower limb Spirals Handwriting Dot approximation Standing
Time frame: Will occur right after the consent received from patients during the first lab visit.
Motor UHDRS for HD (Unified Huntington's Disease Rating Scale: Reliability and Consistency)
OCULAR PURSUIT (horizontal and vertical) SACCADE INITIATION (horizontal and vertical) SACCADE VELOCITY (horizontal and vertical) DYSARTHRIA TONGUE PROTRUSION MAXIMAL DYSTONIA (trunk and extremities) MAXIMAL CHOREA (face, mouth, trunk and RETROPULSION PULL TEST FINGER TAPS (right and left) PRONATE/SUPINATE-HANDS (right and left) LURIA RIGIDITY-ARMS (right and left) BRADY KINESIA-BODY GAIT TANDEM WALKING
Time frame: Will occur right after the consent received from patients during the first lab visit.
(UDRS) Unified Dystonia Rating Scale
Eyes and upper face Lower face Jaw and tongue Larynx Neck Shoulder and proximal arm (right and left) Distal arm and hand including elbow Pelvis and proximal leg (right and left) Distal leg and foot including knee Trunk
Time frame: Will occur right after the consent received from patients during the first lab visit.
(BARS) Brief Ataxia Rating Scale
To develop a brief ataxia rating scale (BARS) for use by movement disorder specialists and general neurologists. BARS is valid, reliable, and sufficiently fast and accurate for clinical purposes.
Time frame: Will occur right after the consent received from patients during the first lab visit.
(s-FMDRS) Simplified Functional Movement Disorders Rating Scale
The Psychogenic Movement Disorders Rating Scale (PMDRS) has potential as a useful objective assessment in clinical research
Time frame: Will occur right after the consent received from patients during the first lab visit.
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