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Re-Step: Dynamic Balance Treatment of Gait for Acquired Brain Injury (ABI) Victims

Primary Purpose

Acquired Brain Injury

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Re-Step
Sponsored by
Reuth Rehabilitation Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acquired Brain Injury focused on measuring Postural balance, Motor Learning and Motor Control, Community integration, Quality of life, Functional ambulation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • At least one year after the Acquired brain injury.
  • Age 18 to 80 years
  • Independent walking ability for at least 10 meters
  • Patients who permanently use medications that have not been changed during the past month and with no further changes expected during the research
  • At least 19 points on the MoCA test

Exclusion Criteria:

  • Presence of degenerative neurological disability that is not secondary to the acquired brain injury
  • Other disabilities such as - severe back pain, radical active lumbosacral radicular pain, leg muscle pain, peripheral neuropathy, post-polio syndrome, rheumatic illnesses, previous orthopedic disabilities preceding or at the time of the injury that could affect the ability and pattern of walking, depression, and other neurotic syndromes including post-traumatic depression and post-traumatic stress disorder (PTSD) at a medium level or higher, chronic alcoholism and use of drugs.
  • Unstable state of health such as heart disease, respiratory insufficiency, peripheral vascular disease, acquired brain injury that has impaired walking ability
  • Inability to persevere and cooperate in the series of tests and the follow-up

Sites / Locations

  • Reuth Rehabilitation Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Re-Step

Arm Description

The system consists of a pair of special shoes which sole height and angles change in a specific given order, thereby facilitating motor learning and problem solving in real time. This unpredictable change will introduce a situation of necessary adaptation to keep balance.

Outcomes

Primary Outcome Measures

Community Balance & Mobility Scale (CB&M); Change from base line after intervention is being assessed
CB&M was designed to evaluate balance and mobility in patients who, although ambulatory, have balance impairments that reduce their full engagement in community living. 13 items of dynamic balance are graded 0-5 by a physiotherapist. The CB&M is a reliable and valid clinical outcome measure for evaluating change in ability in the higher functioning ambulatory patients with TBI.

Secondary Outcome Measures

10 Meter walk Test (10MWT)
Assesses walking speed in meters per second over a short duration. The individual is instructed to walk a set distance (6 meters, 10 meters, etc). Time is measured while the individual walks the set distance (often the individual is given space to accelerate to his/her preferred walking speed (this distance is not included when determining speed). The distance covered is divided by the time it took the individual to walk that distance.
Montreal Cognitive Assessment (MoCA)
Widely used method for assessing cognitive mental status both in clinical practice and in research. It is a brief, standardized method to grade patients' cognitive mental status. It assesses orientation, attention, immediate and short-term recall, language, and the ability to follow simple verbal and written commands. It provides a total score that places the individual on a scale of cognitive function. The MoCA test has a high sensitivity for detecting cognitive dysfunction.
fMRI functional magnetic Resonance Imaging; Change from base line after intervention is being assessed
Functional magnetic resonance imaging or functional MRI (fMRI) is a functional neuroimaging procedure using MRI technology that measures brain activity by detecting associated changes in blood flow. This technique relies on the fact that cerebral blood flow and neuronal activation are coupled. When an area of the brain is in use, blood flow to that region also increases.

Full Information

First Posted
July 24, 2014
Last Updated
March 9, 2021
Sponsor
Reuth Rehabilitation Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02215590
Brief Title
Re-Step: Dynamic Balance Treatment of Gait for Acquired Brain Injury (ABI) Victims
Official Title
Re-Step: a Computerized Dynamic Balance Treatment for Rehabilitation of Unassisted Gait in ABI Victims: a Prospective, Exploratory and Interventional Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
May 30, 2018 (Actual)
Study Completion Date
May 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Reuth Rehabilitation Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to: Test the walking functionality of people following Acquired brain injury (ABI) Suggesting a new treatment for their walking impairments Follow-up of motor learning ability and balance after intervention within this population The investigators intend to target dynamic stability and gait after ABI, in a group of individuals with ABI who have persistent balance and mobility deficits despite being able to walk independently and having high scores on standard clinical balance measures. Interventions: Training with Re-Step system shoes. In this study there is no control group.
Detailed Description
Study design: Type of research: Prospective, exploratory, clinical, interventional trial Specific objectives are: To explore the efficacy of Re-step rehabilitation technology to improve dynamic balance in the gait of people after Acquired Brain Injury (ABI). The investigators suggest a new technology of intervention that will induce unexpected changes of underfoot slopes, with Re-Step shoes, during walking and will force the central nervous system (CNS) to react and solve walking problems in real-time. The investigators propose that the new approach will have a significant motor function improvement on balance in gait, transferred to real environmental settings and be retained for long periods of time. Research methods: Subjects: A total of 40 subjects of ABI victims will be studied in one treatment group-Re-Step shoes walking training Time flow protocol: Participants will be approached using a database of hospitalized patients of Reuth Rehabilitation Hospital (Tel-Aviv, Israel) and through a call for participation placed in a newspaper. Subjects will be recruited according to inclusion/exclusion criteria, after medical examination and given consent of participation. Tests and measures (see outcome measures) will be applied to measure changes: T1 - before starting the intervention to form a baseline T2 - after 20 sessions of intensive treatments 60 min each, 2 sessions a week. T3 - 6 months after T2, a period of normal daily schedule of subjects, with no interventions, to examine for retainment of training results. The treatments will start in a week from T1; the T2 will be performed in a week after training was completed; T3 will be performed 6 months (take or leave 2 weeks) after T2.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acquired Brain Injury
Keywords
Postural balance, Motor Learning and Motor Control, Community integration, Quality of life, Functional ambulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Re-Step
Arm Type
Experimental
Arm Description
The system consists of a pair of special shoes which sole height and angles change in a specific given order, thereby facilitating motor learning and problem solving in real time. This unpredictable change will introduce a situation of necessary adaptation to keep balance.
Intervention Type
Device
Intervention Name(s)
Re-Step
Other Intervention Name(s)
Step of Mind's Re-Step System shoes
Intervention Description
Research Group: Each session begins with a warm-up exercise, muscle stretching, and strengthening exercises: duration 10 minutes. Afterwards, walking exercises for 40 minutes with Re-Step according to a program individually tailored and progressing with the training. Progress is shown by an increased range of tilting of the shoe and speed of changes, according to the individual ability of each patient. At the end of the session 10 min of cool-down exercises 22 training sessions of 60 minutes each, twice a week.
Primary Outcome Measure Information:
Title
Community Balance & Mobility Scale (CB&M); Change from base line after intervention is being assessed
Description
CB&M was designed to evaluate balance and mobility in patients who, although ambulatory, have balance impairments that reduce their full engagement in community living. 13 items of dynamic balance are graded 0-5 by a physiotherapist. The CB&M is a reliable and valid clinical outcome measure for evaluating change in ability in the higher functioning ambulatory patients with TBI.
Time Frame
Measuring mobility ability and balance at base line and changes after intervention; and changes and rtainment of achievments 6 months of no intervention
Secondary Outcome Measure Information:
Title
10 Meter walk Test (10MWT)
Description
Assesses walking speed in meters per second over a short duration. The individual is instructed to walk a set distance (6 meters, 10 meters, etc). Time is measured while the individual walks the set distance (often the individual is given space to accelerate to his/her preferred walking speed (this distance is not included when determining speed). The distance covered is divided by the time it took the individual to walk that distance.
Time Frame
Measuring at base line; change immediately after intervention, and changes and retainments of achievments after 6 months
Title
Montreal Cognitive Assessment (MoCA)
Description
Widely used method for assessing cognitive mental status both in clinical practice and in research. It is a brief, standardized method to grade patients' cognitive mental status. It assesses orientation, attention, immediate and short-term recall, language, and the ability to follow simple verbal and written commands. It provides a total score that places the individual on a scale of cognitive function. The MoCA test has a high sensitivity for detecting cognitive dysfunction.
Time Frame
Recruitment stage
Title
fMRI functional magnetic Resonance Imaging; Change from base line after intervention is being assessed
Description
Functional magnetic resonance imaging or functional MRI (fMRI) is a functional neuroimaging procedure using MRI technology that measures brain activity by detecting associated changes in blood flow. This technique relies on the fact that cerebral blood flow and neuronal activation are coupled. When an area of the brain is in use, blood flow to that region also increases.
Time Frame
Base line brain activity; change after treatment; and change after 6 months with no interventions

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least one year after the Acquired brain injury. Age 18 to 80 years Independent walking ability for at least 10 meters Patients who permanently use medications that have not been changed during the past month and with no further changes expected during the research At least 19 points on the MoCA test Exclusion Criteria: Presence of degenerative neurological disability that is not secondary to the acquired brain injury Other disabilities such as - severe back pain, radical active lumbosacral radicular pain, leg muscle pain, peripheral neuropathy, post-polio syndrome, rheumatic illnesses, previous orthopedic disabilities preceding or at the time of the injury that could affect the ability and pattern of walking, depression, and other neurotic syndromes including post-traumatic depression and post-traumatic stress disorder (PTSD) at a medium level or higher, chronic alcoholism and use of drugs. Unstable state of health such as heart disease, respiratory insufficiency, peripheral vascular disease, acquired brain injury that has impaired walking ability Inability to persevere and cooperate in the series of tests and the follow-up
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simona Bar-Haim, PhD; PT
Organizational Affiliation
The Laboratory for Rehabilitation and Motor Control of Walking Faculty of Health Sciences at Ben-Gurion University of the Negev Israel
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean-Jacques Vatine, Dr.
Organizational Affiliation
Reuth Rehabilitation Hospital Tel-Aviv Israel.
Official's Role
Study Director
Facility Information:
Facility Name
Reuth Rehabilitation Hospital
City
Tel-Aviv
ZIP/Postal Code
6772829
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
34739006
Citation
Joubran K, Bar-Haim S, Shmuelof L. Dynamic balance recovery in chronic acquired brain injury participants following a perturbation training. Int J Rehabil Res. 2021 Dec 1;44(4):350-357. doi: 10.1097/MRR.0000000000000485.
Results Reference
derived

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Re-Step: Dynamic Balance Treatment of Gait for Acquired Brain Injury (ABI) Victims

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