Based on promising results of studies on sensory substitution, it is hypothesised that vibrotactile feedback provided to a complete SCI patient improves the performance with an exoskeleton.
ID
Bron
Verkorte titel
Aandoening
People with a complete spinal cord injury (AISA A or B)
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Concerning standing performance
- The maximal weight transfer onto a single limb during a standing lateral weight-shifting exercise
- Mean velocity of the centre of pressure during quiet stance
Concerning gait performance
- Walked distance during approximately one minute of straight walking
Achtergrond van het onderzoek
Rationale: Complete Spinal Cord Injury (SCI) patients lack motor function below the level of lesion and are wheelchair dependent. Exoskeletons give complete SCI patients the ability to walk individually. Although exoskeletons generate the basic motions for ambulation, postural stability has to be maintained by the user. However, the ability of complete SCI patients to maintain postural stability is affected. This is because complete SCI patients miss essential somatosensory information from below their level of lesion. Hence, walking in an exoskeleton is demanding and crutches are necessary to maintain balance.
When sensory information of a specific system is lost, the lack of sensory information can be substituted by providing feedback to another sensory system. As sensory feedback has shown to improve postural control in patients missing essential sensory information, such sensory substitution may also be effectively incorporated in complete SCI patients using an exoskeleton.
Objective: The aim of this study is to investigate the effect of discrete vibrotactile feedback of mediolateral weight shift and step initiation for complete SCI patients on the use of an exoskeleton.
Study design: The proposed study is an experimental pilot study.
Study population: Ten complete SCI patients (American Spinal Injury Association Impairment Scale (ASIA) A or B), who previously participated in the exoskeleton training program of the Sint Maartenskliniek and are able to walk individually, are included.
Main study parameters/endpoints: The primary outcome measures are the maximal weight transfer onto a single limb during a standing lateral weight-shifting exercise, the mean velocity of the centre of pressure during quiet stance and the walked distance during one minute of straight walking.
Doel van het onderzoek
Based on promising results of studies on sensory substitution, it is hypothesised that vibrotactile feedback provided to a complete SCI patient improves the performance with an exoskeleton.
Onderzoeksopzet
Two sessions of one and a half hour.
Onderzoeksproduct en/of interventie
In this experimental pilot study complete SCI patients, who previously participated in the exoskeleton training program of the Sint Maartenskliniek, are included. In the first session, subjects will start with a training session of one hour to become familiar with the vibrotactile feedback system during standing and walking in an exoskeleton. Subsequently, an experimental session of half an hour will follow in which the subjects will perform stance exercises while vibrotactile feedback is alternately present or absent. Within a week, subjects complete another experimental session of one and a half hour in which they will perform gait exercises while sensory feedback of different modalities is alternately present or absent.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- SCI classification ASIA A or B
- Level of SCI between T1 and L1
- Age ≥ 18
- Having experience with the ReWalk exoskeleton and able to walk without a physiotherapist
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Somatosensory problems prior to the complete SCI
- Visual or auditory problems that are not resolved with glasses or a hearing device
- Insufficient mastery of the Dutch language
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Toelichting
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL9107 |
CCMO | NL74476.091.20 |
OMON | NL-OMON49102 |