SAFEWALKER Contribution to the Rehabilitation of Older People After a Post-fall Syndrome (SAFEER)

Toulouse University Hospital

Status: Completed

Conditions: Post-fall Syndrome

Treatments: Device: SAFEWALKER

Study type: Interventional

Funder types: Other

Identifiers

NCT02485171

RC31/14/7420

Details and patient eligibility

About

The main objective of this study is to evaluate the feasibility and acceptability of the use of the robot "SAFEWALKER" complement classical rehabilitation in a group of elderly patients over 70 years during the rehabilitation of post-fall syndrome.

Full description

The post-fall syndrome is an acute functional complications of falls that affects nearly one in five elderly fallers. It combines phobia of the previous vacuum, axial and hypertension astasia abasia.

Unrecognized and untreated, it progresses to a major regressive syndrome, severe physical, psychological and social implications. Only an early rehabilitation for an early resumption of walking, prevents such a development.

The main element is to support and encourage the subject to walking. In practice, it was found that the physiotherapist can not be present daily and the duration of its intervention is often short-lived.

This study will examine the contribution of a medical device of a walking aid (SAFEWALKER the robot) in the rehabilitation and empowerment of seniors with a post-fall syndrome. The SAFEWALKER, which is a walking aid device (http://www.safewalker.com), completes the support action exercised by a third person, by reducing support and securing travel. It allows the subject to move alone at will and is a continuity in relation to the management of the physiotherapist, a potential source of motivation.

The hypothesis is that the SAFEWALKER device can be complementary to the walking rehabilitation in post-fall syndrome.

Enrollment: 20 patients

Sex: All

Ages: 70+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients hospitalized for the treatment of post-fall syndrome

Exclusion criteria

• Demential pathology (Mini Mental State <20)
• Parkinson's disease and other degenerative neurological disorders
• Stroke sequelae
• Fractures members in the previous 12 months
• Lower limb prostheses in place within 6 months prior
• Psychiatric disease
• Presence of mucocutaneous lesions perineal
• Obesity (weight >120 kg)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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20 participants in 2 patient groups

Experimental

Experimental group

Description:

Introduction of a walking aid device SAFEWALKER for elderly patients during rehabilitation after a post-fall syndrome.

Treatment:

Device: SAFEWALKER

No intervention

No Intervention group

Description:

No introduction of a walking aid device for elderly patients during rehabilitation after a post-fall syndrome.