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Robotic support in gait training for neurological patients

Robotic support in gait training for neurological patients - Robotic support in gait training

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON44012
Enrollment
50
Registered
2010-11-04
Start date
2011-02-14
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cerebrovascular accident / spinal cord injury Myelopathy Stroke

Interventions

None listed

Sponsors

Universiteit Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In general the inclusion criteria are: -age > 18 years - a stable medical condition - a physical condition which allows for 3 minutes of supported walking - have sufficient cognitive abilities (Mini-Mental State Examination * 22);Specifically inclusion criteria for spinal cord injury patients are: - a first ever SCI - time since injury > 6 months - complete or incomplete lesion (AIS A,B, C or D) - injury to the spinal cord from below C6, on at least one side of the body - able to sit unsupported (to sit upright without using the hands or an external support);Stroke patients are explicitly included in the study if they: - are diagnosed with a hemiparesis as the result of a stroke - have had the stroke > 6 months ago - score 1 to 4 on the functional ambulation classification - have sufficient communication abilities (Utrechtse Communicatie Onderzoek * 3)

Exclusion criteria

Exclusion criteria: Spinal cord injury patients and stroke patients are excluded if they: - have current orthopaedic problems - other neurological diseases - have a history of cardiac conditions that interfere with physical load - had no independent ambulation prior to SCI or stroke, - have contraindication for lower extremity weight bearing (chronic joint pain, fracture) - inappropriate or unsafe fit of the robotic trainer due to the participant*s body size (bodyweight > 100 kg) and/ or joint contractures. - have spin-stabilizing devices for whom their treating surgeon contraindicates gait - have pressure sore stage 2 or higher

Design outcomes

Primary

MeasureTime frame
The feasibility of a control algorithm will be assessed based on its ability to provide the patient with the required support in a safe and comfortable way, its ability to bring about the desired walking pattern

Secondary

MeasureTime frame
The measured muscle activity will be used to determine whether the control algorithm encourages patients in self generating muscle activity. The responses in the joint movements to the robotically applied forces will be used to derive the subject specific impairments.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)