Assessment of vGRF Measurement During Walking With Feetme® Insoles in Healthy Adults (FeetMe-GRF)

FeetMe

Status: Completed

Conditions: Healthy Volunteers

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT06027762

2021-A02409-32

Details and patient eligibility

About

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) .

Enrollment: 37 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria.

Volunteers with following criteria satisfied:

• Between the ages of 18 and 80.
• Shoe size between 35 to 46.
• Body weight from 40kg to 120kg.
• Able to walk for 30 mins without assistance.
• Comfortable with using a smartphone.

Non-inclusion Criteria.

A volunteer will not be included if one of the following conditions is met:

• cognitive or behavioral problems limiting communication or participation in the study
• deprivation of liberty by a legal or administrative decision
• adults subject to a legal protection measure or unable to express their consent
• pregnant, parturient and nursing mothers
• people admitted to a health or social establishment for purposes other than research
• Past or planned surgery with the possibility of impacting walking in the past 3 months or which had an impact on walking: orthopedic surgery, trauma to the lower limbs and spine, urological or gynecological surgery, brain and spinal cord surgery .
• Chronic disease affecting walking: Rheumatological, orthopedic, painful, neurological pathology.

Trial design

37 participants in 1 patient group

Single-Groupe