Spinocerebellar ataxia

Developing digital tools for objective assessment of disease symptoms in spinocerebellar ataxia.

Spinocerebellar ataxia (SCA) is a group of hereditary ataxias that are characterized by progressive problems with movement. SCA symptoms can vary depending on the specific type and severity of the condition, but they generally involve progressive issues with movement and coordination.

Our research in SCA is focused on establishing the clinical validity of using wearable sensors for objective assessment of disease symptoms in different types of CMT disease.

Our clinical study in SCA

BioDigit SCA

Status: completed
Number of participants: 18
Monitoring period: 1 clinical visit
Study product:  LEGSys

Our research partners

If you're interested in discussing our research, including access to our study protocol and data, or using our products in your clinical trials and research, please contact us.

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