Clinical grade Gait Analysis, validated through nine years of research. Proven and reliable measurement of temporal and spatial gait parameters as well as gait variability and gait symmetry. Record data for multiple walking tasks (including 6 minute walk, 30 metre walk and 25 foot walk).
Identify gait impairment and gait change
Kinesis Gait™ uses gait analysis to identify specific gait and mobility problems by comparing of patient data (e.g. gait variability, gait symmetry) to average values for age and gender. The results are colour coded to highlight mobility impairment.
Measure how well a patient responds to intervention, therapy or medication by trending gait data over time, as well as viewing all historical tests.
Objective assessment of each element of gait including, spatial gait parameters, temporal gait parameters, gait variability and gait symmetry. Customise results by pinning most relevant data to the summary results screen. Identify gait impairment - Data are colour-coded to highlight any statistical deviations in gait measures when compared to reference values.
Intuitive display of results, ability to track use of mobility aids or turn off timing limits.
Prompt and friendly user support.
Add notes on patient gait assessments. Export all patient gait analysis results in Excel format. Create both patient and clinician facing reports on each gait test, in PDF format. HIPAA compliant - Securely and automatically back-up gait analysis results to the cloud.
Over 8 years of dedicated
scientific research has gone
into developing our Gait assessment platform
Fast, low-cost and portable assessment of gait
Using wearable inertial
sensors for accurate
gait analysis and assessment of mobility
GDPR/HIPAA compliant technology
Integrated, secure solution to
backup gait analysis data to remote
server via Wi-Fi
For ease of reference
and onward referral
Product is a registered Class I medical device in the EU,
under the MDD and carries the CE mark.
Kinesis Gait™ is HIPAA compliant and registered with the FDA as a Class I (exempt) medical device in the USA,
is registered as a Class I medical device with Health Canada,
and is registered with the Therapeutic Goods Administration (TGA) in Australia.
Product has been certified for electrical safety to medical device safety standard EN 60601-1.