Parkiwatch
Overview
Koios Care’s Parkiwatch is a Class IIa Software as a Medical Device (EU MDR 2017/745) designed for the continuous, passive detection and quantitative assessment of kinematic patterns in adults with Parkinson’s Disease. It focuses on identifying tremor, bradykinesia, and dyskinesia. The tool utilizes everyday devices like Android smartphones and compatible smartwatches to collect data in the background, without requiring clinic-grade hardware or daily diaries. This data is then transformed into validated kinematic measures and supportive digital health measures. Parkiwatch aims to bridge the gap between infrequent clinic visits and the continuous, fluctuating nature of Parkinson’s symptoms, providing healthcare professionals with objective information to interpret alongside their clinical assessment. It does not diagnose Parkinson’s Disease, recommend or change medication, or replace the judgment of healthcare professionals.
Reviewed by Pouyan Golshani, MD — Interventional Radiologist
Key Features
- Continuous, passive detection of kinematic patterns
- Quantitative assessment of tremor, bradykinesia, and dyskinesia
- Utilizes Android smartphones and compatible smartwatches
- Background data collection
- Objective kinematic measures
- Dashboard and PDF reports for healthcare professionals
- Supports decentralized clinical trials for pharma
- Validated by peer-reviewed publications and research
Use Cases
- Remote monitoring of Parkinson's disease symptoms
- Providing objective data between clinic visits for clinicians
- Empowering patients with objective insights into their condition
- Facilitating decentralized clinical trials for pharmaceutical companies
- Research into Parkinson's disease kinematics
Details
| Category | N/A |
| Pricing | Paid — For patients: €20 / month; For clinicians & hospitals: unknown; For pharma & research: unknown |
| Deployment | Cloud-based |
| Compliance | |
| BAA Available | Unknown |
| HIPAA Compliant | Unknown |
| FDA Status |
Not applicable AI-estimated Parkiwatch is a Class IIa Software as a Medical Device under EU MDR 2017/745, not FDA cleared. It does not diagnose Parkinson’s Disease, recommend or change medication, or replace the judgment of healthcare professionals. |
| Integrations | |
| EHR | Not specified |
| Specialties | All specialties |
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