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A Comparison Between the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training Early After Stroke (HAL-RCT)

Primary Purpose

Stroke, Gait, Hemiplegic, Ambulation Difficulty

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Hybrid Assistive Limb (HAL); gait training
Control Group; Conventional gait training
Sponsored by
Danderyd Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Rehabilitation, Robotics

Eligibility Criteria

18 Years - 67 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • less than 8 weeks since stroke onset; inability to walk independently due to lower extremity paresis (i.e. FAC score 0-1), able to sit on a bench with or-without supervision at least five minutes; sufficient postural control to allow upright position in standing with aids and/or manual support; ability to understand training instructions as well as written and oral study information and to express informed consent; body size compatible with the HAL suit.

Exclusion Criteria:

  • contracture restricting gait movements at any lower limb joint; cardiovascular or other somatic condition incompatible with intensive gait training; and severe, contagious infections.

Sites / Locations

  • Department of Rehabilitation Medicine, Danderyd Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Study Group

Control Group

Arm Description

Intervention: Hybrid Assistive Limb (HAL); gait training in combination with conventional training. Training with the exosceleton Hybrid Assistive Limb (HAL) is performed in 1 session per day, 4 days per week during 4 weeks. Time for each session is individualised but does not exceed 60 minutes/session (effective time). Training with HAL is performed in combination with body-weight support system and on a treadmill. The training program is performed by 2 physiotherapists, who have been trained in the HAL method.

Intervention: Conventional gait training is individualized and performed according to current practice (approximately 30-60 minutes/session, 5 days a week) and may include standing, weight shifting, stepping, over ground walking with assistance and/or assistant devices as well as the use of a treadmill and body weight support. Conventional gait training is offered to both study groups.

Outcomes

Primary Outcome Measures

Change in Functional Ambulation Categories (FAC)
Level of independence in walking, range 0-5

Secondary Outcome Measures

Full Information

First Posted
February 13, 2015
Last Updated
May 17, 2017
Sponsor
Danderyd Hospital
Collaborators
University of Tsukuba
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1. Study Identification

Unique Protocol Identification Number
NCT02410915
Brief Title
A Comparison Between the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training Early After Stroke
Acronym
HAL-RCT
Official Title
Gait Training Early After Stroke - a Comparison Between Training With the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
May 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Danderyd Hospital
Collaborators
University of Tsukuba

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Overall aim is to evaluate HAL for gait training early after stroke and the effect of HAL on short- and long-term functioning, disability and health compared to conventional gait training as part of an inpatient rehabilitation program early after stroke.
Detailed Description
To compare outcome after 4 weeks of gait training with HAL vs. 4 weeks of conventional gait training as part of a regular inpatient rehabilitation program for hemiparetic patients with severely limited mobility early after stroke. Study design: Randomized, controlled study with blinded outcome assessment. Conventional gait training is individualized and performed according to current practice (approximately 30-60 minutes/session, 5 days a week) and may include standing, weight shifting, stepping, over ground walking with assistance and/or assistant devices as well as the use of a treadmill and body weight support. Conventional gait training is offered to both study groups. Training with HAL is performed in 1 session per day, 4 days per week during 4 weeks. Time for each session is individualised but does not exceed 60 minutes/session (effective time). Training with HAL is performed in combination with body-weight support system and on a treadmill. The training program is performed by 2 physiotherapists, who have been trained in the HAL method.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Gait, Hemiplegic, Ambulation Difficulty, Hemiparesis
Keywords
Rehabilitation, Robotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study Group
Arm Type
Experimental
Arm Description
Intervention: Hybrid Assistive Limb (HAL); gait training in combination with conventional training. Training with the exosceleton Hybrid Assistive Limb (HAL) is performed in 1 session per day, 4 days per week during 4 weeks. Time for each session is individualised but does not exceed 60 minutes/session (effective time). Training with HAL is performed in combination with body-weight support system and on a treadmill. The training program is performed by 2 physiotherapists, who have been trained in the HAL method.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
Intervention: Conventional gait training is individualized and performed according to current practice (approximately 30-60 minutes/session, 5 days a week) and may include standing, weight shifting, stepping, over ground walking with assistance and/or assistant devices as well as the use of a treadmill and body weight support. Conventional gait training is offered to both study groups.
Intervention Type
Device
Intervention Name(s)
Hybrid Assistive Limb (HAL); gait training
Other Intervention Name(s)
Hybrid Assistive Limb (HAL)
Intervention Description
Training with HAL is performed in 1 session per day, 4 days per week during 4 weeks. Time for each session is individualised but does not exceed 60 minutes/session (effective time). Training with HAL is performed in combination with body-weight support system and on a treadmill. The training program is performed by 2 physiotherapists, who have been trained in the HAL method.
Intervention Type
Other
Intervention Name(s)
Control Group; Conventional gait training
Intervention Description
Conventional gait training is individualized and performed according to current practice (approximately 30-60 minutes/session, 5 days a week) and may include standing, weight shifting, stepping, over ground walking with assistance and/or assistant devices as well as the use of a treadmill and body weight support. Conventional gait training is offered to both study groups.
Primary Outcome Measure Information:
Title
Change in Functional Ambulation Categories (FAC)
Description
Level of independence in walking, range 0-5
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Other Pre-specified Outcome Measures:
Title
Change in Gait Deviation Index (GDI)
Description
Gait pattern function will be assessed using a motion capture system (Vicon MX40, Oxford, UK) with two force plates (Kistler, Winterthur, Switzerland) and wireless surface electromyography (EMG, Noraxon, Scottsdale, Arizona, USA). Markers will be placed according to a conventional full-body model (Vicon Plug-in-Gait) and surface EMGs, according to standardized electrode placement (www.seniam.org).
Time Frame
After 4 weeks of training and 6 months after stroke
Title
Change in GDI-kinetic.
Description
Gait pattern function will be assessed using a motion capture system (Vicon MX40, Oxford, UK) with two force plates (Kistler, Winterthur, Switzerland) and wireless surface electromyography (EMG, Noraxon, Scottsdale, Arizona, USA). Markers will be placed according to a conventional full-body model (Vicon Plug-in-Gait) and surface EMGs, according to standardized electrode placement (www.seniam.org).
Time Frame
After 4 weeks of training and 6 months after stroke
Title
Change in Barthel Index
Description
Independence in mobility and personal care
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Change in Fugl-Meyer for Lower extremities
Description
Sensory and motor function in lower extremities
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Change in Berg Balance scale
Description
Balance
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Change in Modified Aschworth scale
Description
Spasticity
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Change in 2 minutes walk test
Description
Walking
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Change in Alberts test
Description
Neglect
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Change in EQ5D
Description
Health outcome
Time Frame
Assessed at baseline, after 4 weeks of training and 6 months after stroke
Title
Stroke impact scale
Description
Functioning and disability
Time Frame
6 months after stroke

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
67 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: less than 8 weeks since stroke onset; inability to walk independently due to lower extremity paresis (i.e. FAC score 0-1), able to sit on a bench with or-without supervision at least five minutes; sufficient postural control to allow upright position in standing with aids and/or manual support; ability to understand training instructions as well as written and oral study information and to express informed consent; body size compatible with the HAL suit. Exclusion Criteria: contracture restricting gait movements at any lower limb joint; cardiovascular or other somatic condition incompatible with intensive gait training; and severe, contagious infections.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jörgen Borg, Professor
Organizational Affiliation
Department of Rehabilitation medicine, Danderyd Hospital, Karolinska Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Rehabilitation Medicine, Danderyd Hospital
City
Danderyd
State/Province
Stockholm
ZIP/Postal Code
18288
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
24890413
Citation
Nilsson A, Vreede KS, Haglund V, Kawamoto H, Sankai Y, Borg J. Gait training early after stroke with a new exoskeleton--the hybrid assistive limb: a study of safety and feasibility. J Neuroeng Rehabil. 2014 Jun 2;11:92. doi: 10.1186/1743-0003-11-92.
Results Reference
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A Comparison Between the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training Early After Stroke

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