Outcomes Associated With Progressive Balance And Gait Training Using The KineAssist® Robot

January 18, 2017 updated by: University of Alabama at Birmingham
Using a randomized controlled research design, compare walking outcomes resulting from gait and balance training with standard physical therapist interaction versus training with the addition of a KineAssist® robotic system that provides for safety and freedom of movement.

Study Overview

Detailed Description

Several studies have investigated the use of balance and gait training and have demonstrated significant improvements in walking speed with trained stroke survivors. The inherent risks associated with balance and gait training requires the therapist to be vigilant with providing safety and support during challenging tasks. As a result, consumers are not challenged to their furthest limits and therapists put an inordinate amount of physical effort into safety control. KineAssist® Design, LLC in collaboration with Rehabilitation Institute of Chicago, developed the KineAssist® Balance and Gait Training System (KineAssist®). The KineAssist® is a novel device that allows full freedom of motion for the trunk and pelvis during gait and balance tasks, with additional postural control to enhance balance stability. These functions are available while the device follows the individual overground with minimal interference. The availability of postural control during complex and omnidirectional movement tasks allows the clinician to guarantee consumer safety and body weight support while at the same time provide graded task challenges to the fullest limits of the consumers capabilities. This KineAssist® is revolutionary in that it is the first device that is fully interactive and responsive to the movements and intentions of both the consumer and the therapist during overground challenging balance and gait activities.

Accordingly, the long-term objective of this research is to test the efficacy of robotically enhanced, progressive gait and balance training for improving walking outcomes post-stroke. The following two aims are designed to test whether the KineAssist® provides a more challenging training environment than is typical with physical therapy, and then compares walking outcomes as a result of long-term (6 weeks) training.

Aim: Using a randomized controlled research design, compare walking outcomes resulting from gait and balance training with standard physical therapist interaction versus training with the addition of a KineAssist®t.

Overall, these studies are an important advance for the development of effective clinical interventions for individuals with impaired locomotor ability post-stroke. This study will provide critical information on physiological effects and clinical outcomes and provide important evidence for the use of this new class of robotic technology that accommodates both the clinician and the consumer in stroke rehabilitation.

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alabama
      • Birmingham, Alabama, United States, 35210
        • Locomotor Control Lab

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • > 6 months post-stroke
  • post-stroke hemiparesis
  • 1.0 m/sec or slower walking speed

Exclusion Criteria:

  • musculoskeletal injury
  • recent history of cardiac event
  • other neurological disease or disorders
  • inability to follow three-step commands
  • uncontrolled diabetes and/or high blood pressure

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Standard physical therapist
A combination of nine balance training tasks where the physical therapist provides guarding against loss of balance

Nine balance tasks:

  1. long forward step
  2. forward reach
  3. push forward
  4. push backward
  5. step over hurdle
  6. step up on foam surface
  7. step up on solid surface
  8. sit-to-stand
  9. step onto slippery surface The therapist will provide guarding support
Experimental: standard robotic guarding
A combination of nine balance training tasks where the robotic system provides guarding against loss of balance

Nine balance tasks:

  1. long forward step
  2. forward reach
  3. push forward
  4. push backward
  5. step over hurdle
  6. step up on foam surface
  7. step up on solid surface
  8. sit-to-stand
  9. step onto slippery surface The guarding support will be provided by a robot
Experimental: challenge based robotic guarding
A combination of nine balance training tasks where the robotic system provides guarding against loss of balance while the participant works at a level greater than their current balance capability

Nine balance tasks where the subject is challenged to perform at a harder level of difficulty:

  1. long forward step
  2. forward reach
  3. push forward
  4. push backward
  5. step over hurdle
  6. step up on foam surface
  7. step up on solid surface
  8. sit-to-stand
  9. step onto slippery surface The guarding support will be provided by a robot

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean time of 10 meter walk test at baseline
Time Frame: baseline
baseline
Mean time of 10 meter walk test at 3 weeks post baseline
Time Frame: 3 weeks post baseline
3 weeks post baseline
Mean time of 10 meter walk test at 6 weeks at end of training
Time Frame: 6 weeks post baseline
6 weeks post baseline
Mean time of 10 meter walk test at 6 months post training
Time Frame: 6 months post end of training
6 months post end of training
Mean time of 6 minute walk test at baseline
Time Frame: baseline
baseline
Mean time of 6 minute walk test at 3 weeks post baseline
Time Frame: 3 weeks post baseline
3 weeks post baseline
Mean time of 6 minute walk test at 6 weeks post baseline (end of training)
Time Frame: 6 weeks post baseline (end of training)
6 weeks post baseline (end of training)
Mean time of 6 minute walk test at 6 months post training
Time Frame: 6 months post end of training (7.5 months post baseline)
6 months post end of training (7.5 months post baseline)
Mean Berg Balance Scale score at baseline
Time Frame: baseline
The Berg Balance Scale has a range of 56 (best) to 14 (worst). There are 14 different balance tasks each with a an assigned rank of 1 - 4 (1, 2, 3, 4). 1 is the worst performance and 4 is the best.
baseline
Mean Berg Balance Scale score at 3 weeks post baseline
Time Frame: 3 weeks post baseline
The Berg Balance Scale has a range of 56 (best) to 14 (worst). There are 14 different balance tasks each with a an assigned rank of 1 - 4 (1, 2, 3, 4). 1 is the worst performance and 4 is the best.
3 weeks post baseline
Mean Berg Balance Scale score at 6 weeks post baseline (end of training)
Time Frame: 6 weeks post baseline
The Berg Balance Scale has a range of 56 (best) to 14 (worst). There are 14 different balance tasks each with a an assigned rank of 1 - 4 (1, 2, 3, 4). 1 is the worst performance and 4 is the best.
6 weeks post baseline
Mean Berg Balance Scale score at 6 months post end of training
Time Frame: 6 months post end of training (7.5 months post baseline)
The Berg Balance Scale has a range of 56 (best) to 14 (worst). There are 14 different balance tasks each with a an assigned rank of 1 - 4 (1, 2, 3, 4). 1 is the worst performance and 4 is the best.
6 months post end of training (7.5 months post baseline)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2008

Primary Completion (Actual)

September 1, 2013

Study Registration Dates

First Submitted

October 16, 2016

First Submitted That Met QC Criteria

December 8, 2016

First Posted (Estimate)

December 13, 2016

Study Record Updates

Last Update Posted (Estimate)

January 19, 2017

Last Update Submitted That Met QC Criteria

January 18, 2017

Last Verified

October 1, 2016

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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