Assessment of vGRF Measurement During Walking With FeetmeĀ® Insoles in Healthy Adults (NCT06027762) | Clinical Trial Compass
CompletedNot Applicable
Assessment of vGRF Measurement During Walking With FeetmeĀ® Insoles in Healthy Adults
France37 participantsStarted 2022-02-01
Plain-language 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 FeetMeĀ® insoles compared to force plates (AMTI BP400600) and video motion capture system (Vicon NEXUS and MX-T40) .
Who can participate
Age range18 Years ā 80 Years
SexALL
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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.
What they're measuring
1
precision of measurement of 'maximum weight acceptance' and 'push-off' peaks in healthy adults by FeetMeĀ® insoles
Timeframe: between February 2022 and November 2022