Assessment of vGRF Measurement During Walking With Feetme® Insoles in Healthy Adults (NCT06027762) | Clinical Trial Compass
CompletedNot Applicable
Assessment of vGRF Measurement During Walking With Feetme® 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 FeetMe® insoles compared to force plates (AMTI BP400600) and video motion capture system (Vicon NEXUS and MX-T40) .
Who can participate
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
precision of measurement of 'maximum weight acceptance' and 'push-off' peaks in healthy adults by FeetMe® insoles
Timeframe: between February 2022 and November 2022