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Robot-assisted Gait Training in Multiple Sclerosis Subjects

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Lokomat (Hocoma, Switzerland)
Conventional Therapy
Sponsored by
University Hospital of Ferrara
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring multiple sclerosis, gait rehabilitation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • males and females, community dwelling, age 18 or older
  • diagnosis of multiple sclerosis in a stable phase, with relapses > 6 months prior to study enrollment
  • moderate to severe gait impairments referred to Expanded Disability Status Scale (EDSS) between 6 and 7

Exclusion Criteria:

  • neurologic conditions in addition to multiple sclerosis that may affect motor function
  • medical conditions likely to interfere with the ability to safely complete the study
  • impaired cognitive functioning: Mini Mental Status Examination < 24
  • severe lower-extremities spasticity or contractures that may limit range of motion(Ashworth score >4 for hip, knee or ankle flexors/extensors

Sites / Locations

  • Physical Medicine and Rehabilitation Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Robot-assisted gait training

Conventional Therapy

Arm Description

Subjects will wear a harness attached to a system to provide body weight support and they will walk on a treadmill with the help of a robotic-driven gait orthosis. The legs are guided according to a physiological gait pattern. The torque of the knee and hip drives can be adjusted from 100% to 0% for one or both legs. The speed of the treadmill can be adjusted from 0 km/h to approximately 3 km/h and body weight support from 0% to 100%. Training sessions will last for an hour with 30 minutes of real walking time, because subject set-up in the device take approximately 30 minutes.

Training sessions will focus on locomotor function improvements. Subjects will receive 45 minutes of individual conventional physiotherapy for session. During the first 5-10 minutes the subjects will perform lower-limb and core stretching exercises to increase muscles flexibility; then they'll deal with lower-limb muscles strengthening exercises tailored on their baseline characteristics (10 minutes). After that they will be trained on walking abilities (like walking at different speeds, rapid changes directions) for 30 minutes with or without assistive aids.

Outcomes

Primary Outcome Measures

motor unit firing rate characteristics
It will be performed through the analysis of superficial EMG signals during isometric knee extension.

Secondary Outcome Measures

walking endurance
six minute walking test
mobility
Timed Up and Go Test
balance
Berg Balance Test
gait speed
10 meter test
Fatigue
Fatigue Severy Scale
quality of life
SF-36
depression
patient health questionnaire (PHQ-9)

Full Information

First Posted
September 14, 2011
Last Updated
January 15, 2014
Sponsor
University Hospital of Ferrara
Collaborators
Azienda Ospedaliero, Universitaria Pisana
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1. Study Identification

Unique Protocol Identification Number
NCT01435694
Brief Title
Robot-assisted Gait Training in Multiple Sclerosis Subjects
Official Title
The Effects of Robot-assisted Gait Training on Locomotor Function and Motor Unit Firing in Multiple Sclerosis Subjects With Severe Gait Impairments. A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital of Ferrara
Collaborators
Azienda Ospedaliero, Universitaria Pisana

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Aims of the study: This is a randomized-controlled trial to test the effects of robot-assisted gait training on locomotor function and motor unit firing rate in multiple sclerosis subjects with severe gait impairments. The control group will be treat with conventional physical therapy. Subjects and methods: 60 multiple sclerosis patients will be recruited in two outpatient rehabilitation clinics. Informed consent will be obtained. Participants will be randomized to Robot-assisted gait training (experimental group) or conventional therapy (control group) through a randomization stratification approach, according to a block randomization of 4. The experimental group will receive 12 robot-assisted gait training sessions over 6 weeks (2 sessions/week). The control group will receive 12 conventional therapy sessions over 6 weeks (2 sessions/week), that will focus on gait training. Primary outcome measures will be both neurophysiological measures (motor unit firing rate characteristics) and clinical test for gait speed (10m walking test). Secondary outcome measures will include: clinical tests of walking endurance (six minute walking test), balance (Berg Balance Test) and mobility (Up and Go Test). Clinical assessment of lower-extremities spasticity (Modified Ashworth Scale), motor fatigue (Fatigue Severity Scale), depression (PHQ-9) and quality of life (SF-36) will be monitored. Subject acceptance and confidence in the treatments will be track with a Visual Analog Scale. Outcome measures will be assessed the week prior to treatment initiation (T0), after 6 sessions (T1), the week after the end of treatment (T2) and at 3 months follow-up (T3) to evaluate treatments retention, by a clinician blinded to the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
multiple sclerosis, gait rehabilitation

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Robot-assisted gait training
Arm Type
Experimental
Arm Description
Subjects will wear a harness attached to a system to provide body weight support and they will walk on a treadmill with the help of a robotic-driven gait orthosis. The legs are guided according to a physiological gait pattern. The torque of the knee and hip drives can be adjusted from 100% to 0% for one or both legs. The speed of the treadmill can be adjusted from 0 km/h to approximately 3 km/h and body weight support from 0% to 100%. Training sessions will last for an hour with 30 minutes of real walking time, because subject set-up in the device take approximately 30 minutes.
Arm Title
Conventional Therapy
Arm Type
Active Comparator
Arm Description
Training sessions will focus on locomotor function improvements. Subjects will receive 45 minutes of individual conventional physiotherapy for session. During the first 5-10 minutes the subjects will perform lower-limb and core stretching exercises to increase muscles flexibility; then they'll deal with lower-limb muscles strengthening exercises tailored on their baseline characteristics (10 minutes). After that they will be trained on walking abilities (like walking at different speeds, rapid changes directions) for 30 minutes with or without assistive aids.
Intervention Type
Behavioral
Intervention Name(s)
Lokomat (Hocoma, Switzerland)
Other Intervention Name(s)
robotic-driven gait orthosis
Intervention Type
Behavioral
Intervention Name(s)
Conventional Therapy
Primary Outcome Measure Information:
Title
motor unit firing rate characteristics
Description
It will be performed through the analysis of superficial EMG signals during isometric knee extension.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
walking endurance
Description
six minute walking test
Time Frame
12 months
Title
mobility
Description
Timed Up and Go Test
Time Frame
12 months
Title
balance
Description
Berg Balance Test
Time Frame
12 months
Title
gait speed
Description
10 meter test
Time Frame
12 months
Title
Fatigue
Description
Fatigue Severy Scale
Time Frame
12 months
Title
quality of life
Description
SF-36
Time Frame
12 months
Title
depression
Description
patient health questionnaire (PHQ-9)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: males and females, community dwelling, age 18 or older diagnosis of multiple sclerosis in a stable phase, with relapses > 6 months prior to study enrollment moderate to severe gait impairments referred to Expanded Disability Status Scale (EDSS) between 6 and 7 Exclusion Criteria: neurologic conditions in addition to multiple sclerosis that may affect motor function medical conditions likely to interfere with the ability to safely complete the study impaired cognitive functioning: Mini Mental Status Examination < 24 severe lower-extremities spasticity or contractures that may limit range of motion(Ashworth score >4 for hip, knee or ankle flexors/extensors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sofia Straudi, MD
Organizational Affiliation
Ferrara University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Carmelo Chisari, MD
Organizational Affiliation
Pisana University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nino Basaglia, MD
Organizational Affiliation
Ferrara University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Physical Medicine and Rehabilitation Department
City
Ferrara
ZIP/Postal Code
44100
Country
Italy

12. IPD Sharing Statement

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Robot-assisted Gait Training in Multiple Sclerosis Subjects

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