Study of Locomotor Expectations for Ascending/Descending Slope and Stairs in Patients With Limb Amputations
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Functional analyses, 3D analysis of walking and balance, Functional analyses.
- Who it may be relevant to
- Registry conditions: Lower Limb Amputation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Patients with lower limb amputations are equipped with prostheses that can be mechanical and/or electronic. These prostheses can be mono-articular (only the ankle) or bi-articular (knee and ankle for example). For amputee patients, situations that may seem trivial, such as climbing and descending stairs, become complex. Thus during the descent of stairs, an unamputated person will slow down the descent by contracting the thigh muscles, which are obviously lacking in the amputee patient. Current prostheses, known as "intelligent" (or "microprocessor") prostheses, make it possible to adjust the locomotion only once the first step has been taken and to assist the patient during ascent/descent situations on slopes and stairs. The next technological challenge in the development of lower limb equipment is to be able to anticipate these complex environmental situations, in order to secure and facilitate movement even before the obstacle is crossed or the terrain changed. This project plans to use the locomotor expectations commonly made during walking as a means of regulating the locomotor pattern. We believe that these expectations will depend on the situation, i.e. a particular anticipation when climbing or descending a slope, or when approaching a staircase, etc. To understand and describe these locomotor expectations, we plan to use recent techniques called supervised machine learning. These will make it possible to classify locomotor behaviour when walking on a slope or stairs. In the second phase, we would like to describe precisely the characteristics of the movements of the joints, and of the muscles during these adaptations. The final objective of this work is to create an autonomous sensor system to control the anticipatory behaviour of a lower limb prosthesis.
Interventions
- Other Functional analyses
2-minute walking test 200-metre walking test - Other 3D analysis of walking and balance
Walking analysis Balance analysis Analysis of the strength of the flexor and extensor muscles of the trunk and lower limb - Other Functional analyses
400-metre walking test 200-metre walking test
Primary outcome measures
- The error rate of the algorithm [Time frame: 2 months]
Eligibility criteria
Inclusion criteria
Healthy volunteers:
- person who has given oral consent
- male or female adult
- person being able to understand simple orders, locomotion instructions
Lower limb amputee patients:
- person who has given oral consent
- male or female adult
- patient with unilateral major lower limb amputation of any origin (traumatic, vascular, infectious, congenital or neoplastic) with definitive equipment used routinely for at least 3 months.
- person able to understand simple orders, locomotion instructions
Exclusion criteria
- person not affiliated or not benefiting from a heath insurance system
- person subject to a legal protection measure (curatorship, guardianship)
- person with a legal guardian
- pregnant or breastfeeding woman
- adult unable to consent
- person with a dislocated hip
- subject with conditions or disabilities other than amputation that affect walking
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Other
Study locations
France · 1 center
- CHU Dijon Bourgogne — Dijon
Identifiers
NCT: NCT04030650 · CASILLAS 2018-1