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Stroke Rehabilitation Program Based on a Powered Lower Extremity Exoskeleton in Chile

Stroke Rehabilitation Program Based on a Powered Lower Extremity Exoskeleton in Chile

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04228224
Enrollment
50
Registered
2020-01-14
Start date
2019-07-01
Completion date
2020-03-31
Last updated
2020-07-16

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

Conditions

Stroke

Keywords

Stroke, Hemiparesis, Gait, Brain-Computer Interface, Rehabilitation, Exoskeleton

Brief summary

This research will study the effects of a rehabilitation program assisted by a powered lower extremity exoskeleton in patients after stroke. It will compare clinical and biomechanical features of patients at baseline and after intervention. Additionally, it will also examine the use of a brain-computer-interface (BCI) to command movements on the powered lower limb exoskeleton. The findings will be used to improve understanding human-robot interaction, to improve the design of the robotic devices and to improve rehabilitation services.

Detailed description

Stroke is one of the leading causes of mortality, morbidity and disability in adults in developed countries. Survivors may suffer several neurological deficits or deficiencies, such as hemiparesis, communication disorders, cognitive deficits and visuospatial perception disorders. Hemiplegia is a par loss of hemi-body voluntary motricity following a brain injury, usually resulting in alterations of the locomotor system with persistent disorders of movement and posture. Hemiplegia significantly affects gait performance. Gait recovery is an important objective in the rehabilitation program for stroke patients.The currently available treatment techniques include classical techniques of gait rehabilitation, functional electrical stimulation, electromechanic devices, robotic devices and brain-computer interfaces, among others.The evidence suggest that the combination of different rehabilitation strategies is more effective than conventional rehabilitation techniques alone. Technology-based rehabilitation methods such as robotic devices need more research to demonstrate their effects on gait recovery. This study will assess the effects of a rehabilitation program with a powered lower extremity exoskeleton in people with stroke. Additionally, it will also examine the use of a brain-computer-interface (BCI) to command movements on the powered lower limb exoskeleton. The findings will be used to improve understanding human-robot interaction, to improve the design of the robotic devices and to improve rehabilitation services.

Interventions

DEVICERobot-assisted training with a lower extremity powered exoskeleton (H3 Exoskeleton, Spain)

The H3 is a powered lower extremity exoskeleton with actuated at hips, knees and ankles joints. A novel control software has been design and implemented in this device, which allows selective joint movement and recording of data from each rehabilitation session.

Conventional gait rehabilitation consist in walking and other applicable lower limb exercises performed by participants with assistance of a physical therapist.

Sponsors

Corporación de Rehabilitación Club de Leones Cruz del Sur
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* unilateral lower extremity paresis * haemorrhagic or ischemic stroke * a minimum of six months after the acute infarction/onset of the disease * full passive range of motion in lower extremity or at least at neutral position * be able to stand freely * be able to walk with or without aid for at least 20 meters in less than 2 minutes

Exclusion criteria

* peripheral nervous system pathology * epilepsy * weight over 100 kg * no cognitive ability to follow the study instructions * pregnancy * use of implanted devices * instable lower extremity joints or fixed contracture

Design outcomes

Primary

MeasureTime frameDescription
Gait Deviation Index BaselineBaselineGait Deviation Index will be calculated for each patient using a 3D VICON infra-red camera system.
Gait Deviation Index Post-Intervention12 weeksGait Deviation Index will be calculated for each patient using a 3D VICON infra-red camera system.

Secondary

MeasureTime frameDescription
Distance in 6 Minute Walk Test (6MWT) BaselineBaselineMeasure of the distance a subject covers during an indoor gait on a flat, hard surface in 6 minutes, using assistive devices, as necessary. The test consist in a evaluation of functional exercise capacity and is used as a sub-maximal test of aerobic capacity and endurance.
Distance in 6 Minute Walk Test (6MWT) Post-Intervention12 weeksMeasure of the distance a subject covers during an indoor gait on a flat, hard surface in 6 minutes, using assistive devices, as necessary. The test consist in a evaluation of functional exercise capacity and is used as a sub-maximal test of aerobic capacity and endurance.
Muscle tone measured using modified ashworth scale (MAS) BaselineBaselineTests resistance to passive movement about a joint with varying degrees of velocity. A score of 1 indicates no resistance, and 5 indicates rigidity.
Muscle tone measured using modified ashworth scale (MAS) Post-Intervention12 weeksTests resistance to passive movement about a joint with varying degrees of velocity. A score of 1 indicates no resistance, and 5 indicates rigidity.
Passive range of motion BaselineBaselinePassive range of motion in lower extremities. ROM will be assessed by using an universal goniometer
Passive range of motion Post-Intervention12 weeksPassive range of motion in lower extremities. ROM will be assessed by using an universal goniometer
10 meter walk test BaselineBaselineThe 10 Metre Walk Test is a performance measure used to assess walking speed in metres per second over a short distance. It can be employed to determine functional mobility, gait, and vestibular function.
10 meter walk test Post-Intervention12 weeksThe 10 Metre Walk Test is a performance measure used to assess walking speed in metres per second over a short distance. It can be employed to determine functional mobility, gait, and vestibular function.
Timed Up and Go BaselineBaselineMeasurement of the time in seconds for a person to rise from sitting from a standard arm chair, walk 3 meters, turn, walk back to the chair, and sit down. The person wears regular footwear and customary walking aid.
Maximal muscle strength BaselineBaselineMaximal muscle strength (peak torque, Nm) during maximal voluntary unilateral hip extension-flexion, and hip adduction-abduction (standing), knee extension-flexion (seated), respectively. Both the affected (AF) and non-affected (NA) leg. A hand-held dynamometer will be used for the assessment.
Berg Balance Scale BaselineBaselineBerg balance scale is used for functional balance. participants are asked to perform 14 tasks frequently used in daily life activities. The highest possible score is 56 points. A higher score indicates better balance.
Berg Balance Scale Post-Intervention12 weeksBerg balance scale is used for functional balance. participants are asked to perform 14 tasks frequently used in daily life activities. The highest possible score is 56 points. A higher score indicates better balance.
Functional Ambulation Classification (FAC) BaselineBaselineFAC is a functional walking test that evaluates ambulation ability. This 6-point scale assesses ambulation status by determining how much human support the patient requires when walking, regardless of whether or not they use a personal assistive device.
Functional Ambulation Classification (FAC) Post-Intervention12 weeksFAC is a functional walking test that evaluates ambulation ability. This 6-point scale assesses ambulation status by determining how much human support the patient requires when walking, regardless of whether or not they use a personal assistive device.
Patient satisfaction with device: Quebec User Evaluation of Satisfaction with Assistive Technology12 weeksMeasured with QUEST scale. The Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 2.0) is a 12-item outcome measure that assesses user satisfaction with two components, Device and Services. Scores of 1 indicate dissatisfaction and scores of 5 indicate high satisfaction
Medical Research Council test (MRC) BaselineBaselineManual evaluation of muscle strength. This scale grades muscle power on a scale of 0 to 5 in relation to the maximum expected for that muscle. Grade 0 = no movement is observed, grade 5= muscle contracts normally against full resistance. Six muscles groups are tested at both sides of the body: shoulder abduction, elbow flexion, wrist extension, hip flexion, knee extension, ankle dorsiflexion. Maximal total score is 60.
Medical Research Council test (MRC) Post-Intervention12 weeksManual evaluation of muscle strength. This scale grades muscle power on a scale of 0 to 5 in relation to the maximum expected for that muscle. Grade 0 = no movement is observed, grade 5= muscle contracts normally against full resistance. Six muscles groups are tested at both sides of the body: shoulder abduction, elbow flexion, wrist extension, hip flexion, knee extension, ankle dorsiflexion. Maximal total score is 60.
Gait Speed BaselineBaselineGait Speed will be calculated for each patient using a 3D VICON infra-red camera system.
Gait Speed Post-intervention12 weeksGait Speed will be calculated for each patient using a 3D VICON infra-red camera system.
Timed Up and Go Post-Intervention12 weeksMeasurement of the time in seconds for a person to rise from sitting from a standard arm chair, walk 3 meters, turn, walk back to the chair, and sit down. The person wears regular footwear and customary walking aid.
Maximal muscle strength Post-Intervention12 weeksMaximal muscle strength (peak torque, Nm) during maximal voluntary unilateral hip extension-flexion, and hip adduction-abduction (standing), knee extension-flexion (seated), respectively. Both the affected (AF) and non-affected (NA) leg. A hand-held dynamometer will be used for the assessment.

Countries

Chile

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026