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

Stroke Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04228224
• Other study ID #: CorporacionRCLCS0001
• Status: Completed
• Phase: N/A
• Start date: July 1, 2019
• Est. completion date: March 31, 2020

Study information

• Verified date: July 2020
• Source: Corporación de Rehabilitación Club de Leones Cruz del Sur
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: March 31, 2020
• Est. primary completion date: January 31, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Stroke

Intervention

Device:
• Robot-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.

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

Locations

Country	Name	City	State
Chile	Corporación de Rehabilitación Club de Leones Cruz del Sur	Punta Arenas	XII Región

Sponsors (1)

Lead Sponsor	Collaborator
Corporación de Rehabilitación Club de Leones Cruz del Sur

Country where clinical trial is conducted

Chile, 

References & Publications (4)

Belda-Lois JM, Mena-del Horno S, Bermejo-Bosch I, Moreno JC, Pons JL, Farina D, Iosa M, Molinari M, Tamburella F, Ramos A, Caria A, Solis-Escalante T, Brunner C, Rea M. Rehabilitation of gait after stroke: a review towards a top-down approach. J Neuroeng Rehabil. 2011 Dec 13;8:66. doi: 10.1186/1743-0003-8-66. Review. — View Citation

Bortole M, Venkatakrishnan A, Zhu F, Moreno JC, Francisco GE, Pons JL, Contreras-Vidal JL. The H2 robotic exoskeleton for gait rehabilitation after stroke: early findings from a clinical study. J Neuroeng Rehabil. 2015 Jun 17;12:54. doi: 10.1186/s12984-015-0048-y. — View Citation

Flansbjer UB, Holmbäck AM, Downham D, Patten C, Lexell J. Reliability of gait performance tests in men and women with hemiparesis after stroke. J Rehabil Med. 2005 Mar;37(2):75-82. — View Citation

Wallard L, Dietrich G, Kerlirzin Y, Bredin J. Effects of robotic gait rehabilitation on biomechanical parameters in the chronic hemiplegic patients. Neurophysiol Clin. 2015 Sep;45(3):215-9. doi: 10.1016/j.neucli.2015.03.002. Epub 2015 Sep 14. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Gait Deviation Index Baseline	Gait Deviation Index will be calculated for each patient using a 3D VICON infra-red camera system.	Baseline
Primary	Gait Deviation Index Post-Intervention	Gait Deviation Index will be calculated for each patient using a 3D VICON infra-red camera system.	12 weeks
Secondary	Maximal muscle strength Baseline	Maximal 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.	Baseline
Secondary	Maximal muscle strength Post-Intervention	Maximal 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.	12 weeks
Secondary	Distance in 6 Minute Walk Test (6MWT) Baseline	Measure 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.	Baseline
Secondary	Distance in 6 Minute Walk Test (6MWT) Post-Intervention	Measure 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.	12 weeks
Secondary	Muscle tone measured using modified ashworth scale (MAS) Baseline	Tests resistance to passive movement about a joint with varying degrees of velocity. A score of 1 indicates no resistance, and 5 indicates rigidity.	Baseline
Secondary	Muscle tone measured using modified ashworth scale (MAS) Post-Intervention	Tests resistance to passive movement about a joint with varying degrees of velocity. A score of 1 indicates no resistance, and 5 indicates rigidity.	12 weeks
Secondary	Passive range of motion Baseline	Passive range of motion in lower extremities. ROM will be assessed by using an universal goniometer	Baseline
Secondary	Passive range of motion Post-Intervention	Passive range of motion in lower extremities. ROM will be assessed by using an universal goniometer	12 weeks
Secondary	10 meter walk test Baseline	The 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.	Baseline
Secondary	10 meter walk test Post-Intervention	The 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.	12 weeks
Secondary	Timed Up and Go Baseline	Measurement 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.	Baseline
Secondary	Timed Up and Go Post-Intervention	Measurement 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.	12 weeks
Secondary	Berg Balance Scale Baseline	Berg 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.	Baseline
Secondary	Berg Balance Scale Post-Intervention	Berg 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.	12 weeks
Secondary	Functional Ambulation Classification (FAC) Baseline	FAC 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.	Baseline
Secondary	Functional Ambulation Classification (FAC) Post-Intervention	FAC 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.	12 weeks
Secondary	Patient satisfaction with device: Quebec User Evaluation of Satisfaction with Assistive Technology	Measured 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	12 weeks
Secondary	Medical Research Council test (MRC) Baseline	Manual 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.	Baseline
Secondary	Medical Research Council test (MRC) Post-Intervention	Manual 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.	12 weeks
Secondary	Gait Speed Baseline	Gait Speed will be calculated for each patient using a 3D VICON infra-red camera system.	Baseline
Secondary	Gait Speed Post-intervention	Gait Speed will be calculated for each patient using a 3D VICON infra-red camera system.	12 weeks