The digital health technology (DHT) Syde® provides an end-to-end solution for continuous, real-world assessment of patient movement in clinical studies.
Syde’s wearable sensors continuously capture movement data as patients go about their daily activities. Each night, the sensors are placed on their docking station for battery charging and secure, passive data transfer. This ensures minimal burden on patients and clinical teams while maintaining seamless, high-quality data collection.
In real life, the Syde® sensors continuously record data during the day while the patient wears them.
At night, they are placed on their docking station for battery charging and data uploading.
Once the data is uploaded, Syde’s proprietary algorithms reconstruct 3D trajectories of patient movement to derive clinically meaningful variables.
From passively collected raw sensor data to clinical variables, the Syde platform converts everyday movement into objective, regulatory-grade insights on patient motor function.
High precision sensors for 3D trajectory reconstruction with centimetric accuracy⁴ʼ⁵
Each Syde case contains ready-to-use elements to quickly start data collection:
Our algorithms transform real-world motor patterns into validated clinical endpoints. Syde supports both upper and lower-limb assessments, including SV95C (Stride Velocity 95th Centile, top ambulation speed), the first digital endpoint qualified by the EMA.
At Sysnav Healthcare, we recognize that usability is a critical determinant of patient comfort and compliance in clinical research.
Tests for clinical trials should not be a burden on patients, their families, or clinical teams.
Syde was developed in collaboration with patient associations to ensure ergonomic design, ease of operation, and adaptability across heterogeneous patient populations. Its design integrates seamlessly into daily life, minimizing burden while enabling high-quality motor data collection.
Tests for clinical trials should not be a burden on patients, their families, or clinical teams.
Syde was developed in collaboration with patient associations to ensure ergonomic design, ease of operation, and adaptability across heterogeneous patient populations. Its design integrates seamlessly into daily life, minimizing burden while enabling high-quality motor data collection.
We uphold the highest standards of privacy and security while handling medical data:
Here is an example of a patient-facing instructional video for participants in a clinical study.
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Answers to common questions about integrating Syde platform into your clinical trial.
Standard deployment takes 8 to 12 weeks and includes Syde specific protocol consultation, regulatory documentation preparation, site training, and device shipment. Accelerated timelines are available for urgent trials, and we align with your existing study startup milestones to minimize delays.
We provide periodic data transfers containing validated clinical endpoints in a format compatible with your statistical software. Each delivery includes tailored analyses customized to your protocol requirements, comprehensive quality control reports with patient-level compliance and data completeness metrics, and dedicated support for data interpretation to help your teams understand the endpoint’s clinical significance.
