Assessment of vGRF Measurement During Walking With Feetme® Insoles in Healthy Adults
Completed
- Conditions
- Healthy Volunteers
- Registration Number
- NCT06027762
- Lead Sponsor
- FeetMe
- Brief Summary
The objective of the present study is to demonstrate the validity and reliability of vGRF and other gait parameters measurement in healthy adults while walking with FeetMe® insoles compared to force plates (AMTI BP400600) and video motion capture system (Vicon NEXUS and MX-T40) .
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 37
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method precision of measurement of 'maximum weight acceptance' and 'push-off' peaks in healthy adults by FeetMe® insoles between February 2022 and November 2022 The primary objective of this clinical trial is to quantify precision of measurement of two peaks of vGRF, peaks that correspond to 'maximum weight acceptance' and 'push-off', also called 'heelmax load' and 'toemax load' for healthy adults by FeetMe® insoles compared with Vicon and force plates during a free walk test.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hopitaux Saint-Maurice
🇫🇷Saint-Maurice, Ile-de-France, France