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Predicting Who Benefits From Robotic Walking Training in Neurological Disease

Studies which adults with neurological conditions respond to robotic gait training.

Plain-language title generated from the registry record
Registry title: Clinical and Instrumental Treatment's Predictors in Subjects With Neurological Diseases Using G-EO Robotic System

Key facts

Where
Milan, ItalySee the site

Where in Italy

  • Don Gnocchi FoundationMilan, ItalyTaking people

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Trial details

Who runs it
Fondazione Don Carlo Gnocchi ETS
Trial code
NCT05493514
Record updated
9 August 2022
Original description
The aim of this work is to elaborate a statistical model to predict the effectiveness of robotic treatment in subjects with neurological diseases. The model will be used to understand which subjects are most responsive to this type of treatmentRead full original descriptionShow less

Clinical and Instrumental Treatment's Predictors in Subjects With Neurological Diseases Using G-EO Robotic System: an Observational Longitudinal Study

The aim of this work is to elaborate a statistical model to predict the effectiveness of robotic treatment in subjects with neurological diseases. The model will be used to understand which subjects are most responsive to this type of treatment

Inclusion: Diagnosis of Multiple Sclerosis, Parkinson Disease, Stroke or acquired brain injury; Minimum number of sessions: 10 sessions with the GEO system; Minimum frequency of sessions: 2 per week; Age ≥ 18 years; Ability to walk for at least 10 meters, also with aid; Indication of robotic treatment in the therapeutic plan; Body size suitable for the robotic device; ability to maintain verticality for 7 minutes; ability to maintain the sitting position without support for 30 seconds.

Exclusion: Presence of seizures that may be triggered by the use of the G-EO system; severe limitations of articular range of motion; medical problems compromising walking (e.g. fractures, pain, severe osteoporosis or severe spasticity); Presence of skin lesions in the areas of contact with the device.

ClinicalTrials.gov NCT05493514