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This is a study for a new mechanical transport device adapted to the hemiplegic patients.
Healthy volunteers :
After explaining the protocol and presenting the movement laboratory, the subjects are equipped with reflective markers on the 4 limbs, the trunk and the head. The subjects are installed on a seat positioned in front of 2 force platforms installed on the ground. The seat is equipped with a force platform.
Phase 1 :
After being seated, the subject realizes :
Phase 2:
After being seated, the subject performs a course comprising:
This phase 2 will last 30mn (15mn of course and 15mn of questions).
Hemiplegic subjects :
At each session, the subject is examined by a physician who evaluates the motor control (Fugl Meyer scale), the equilibrium (Berg scale) and the spatial hemineglect (Bergego scale).
Phase 1 is performed except the 3 seat to stand and stand to seat without assistance which are impossible.
Phase 2 is performed. An evaluation of the device over 4 hours is carried out for each subject in therapeutic apartment in simulated living conditions. The validation in living lab is carried out by an ergonomist and by a questionnaire on the comfort and safety of the various steps identified by the ergonomist.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Hemiplegic subjects | Experimental | Testing of a new device for seated-standing passages after undergoing medical evaluation included Fugl Meyer scale, Berg scale and Bergego scale. Phase 1 :
|
|
| Healthy volunteers | Experimental | Testing of a new device for seated-standing passages . Phase 1 :
|
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| New device for seated-standing passages | Device | Phase 1 : The subject perform different seated-standing passages (see "Arm") Phase 2 : After being seated, the subject performs a course comprising:
|
| Measure | Description | Time Frame |
|---|---|---|
| Time required to carry out each step of use of the device | Each step of phase 1 and phase 2 will be timed. | Day 1 |
| Measure | Description | Time Frame |
|---|---|---|
| Record of all adverse reactions. | The safety of the devices will be evaluated by the occurrence of adverse reactions. | Day 1 |
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Inclusion Criteria:
Healthy volunteers :
Hemiplegic patients :
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Brest University Hospital | Brest | 29200 | France | |||
| Centre de rééducation fonctionnelle de KERPAPE |
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| ID | Term |
|---|---|
| D006429 | Hemiplegia |
| ID | Term |
|---|---|
| D010243 | Paralysis |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D012816 | Signs and Symptoms |
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|
| Ploemeur |
| 56000 |
| France |
| D013568 |
| Pathological Conditions, Signs and Symptoms |