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Completed

NCT Number: NCT02410915

A Comparison Between the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training Early After Stroke

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.

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Key information

Age range

18 year–67 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Rehabilitation Medicine, Danderyd Hospital

Danderyd, Stockholm County, 18288, Sweden

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Hybrid Assistive Limb (HAL); gait training

Device

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.

Other names: Hybrid Assistive Limb (HAL)

Control Group; Conventional gait training

Other

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 outcomes

  1. Change in Functional Ambulation Categories (FAC)

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Level of independence in walking, range 0-5

Other outcomes

  1. Change in Gait Deviation Index (GDI)

    Time frame: After 4 weeks of training and 6 months after stroke

    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).

  2. Change in GDI-kinetic.

    Time frame: After 4 weeks of training and 6 months after stroke

    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).

  3. Change in Barthel Index

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Independence in mobility and personal care

  4. Change in Fugl-Meyer for Lower extremities

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Sensory and motor function in lower extremities

  5. Change in Berg Balance scale

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Balance

  6. Change in Modified Aschworth scale

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Spasticity

  7. Change in 2 minutes walk test

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Walking

  8. Change in Alberts test

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Neglect

  9. Change in EQ5D

    Time frame: Assessed at baseline, after 4 weeks of training and 6 months after stroke

    Health outcome

  10. Stroke impact scale

    Time frame: 6 months after stroke

    Functioning and disability

Sponsors and collaborators

Lead sponsor

Danderyd Hospital

Other

Collaborators

  • University of Tsukuba

Registry information

Official study title

Gait Training Early After Stroke - a Comparison Between Training With the Exoskeleton Hybrid Assistive Limb and Conventional Gait Training

Acronym: HAL-RCT

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Apr 8, 2015
Registry last updated
May 18, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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