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Robot-assisted Gait Training in Patients With Multiple Sclerosis: Efficacy and Comparison With Traditional Methods

Primary Purpose

Multiple Sclerosis

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Lokomat (Hocoma, Zurich, Switzerland)
Conventional Physiotherapy
Sponsored by
Habilita, Ospedale di Sarnico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Gait orthosis, Lokomat, Robotic Rehabilitation

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diagnosis of multiple sclerosis according to the McDonald's Criteria in stable phase of disease for at least 3 months.
  • ability to walk 25 foot without assistance
  • EDSS score between 3.5 and 7

Exclusion Criteria:

  • exacerbations of the disease in the last 3 months
  • deficits of somatic sensation involving the legs
  • other neurological, orthopedic or cardiovascular co-morbility
  • severe posture abnormalities
  • severe-moderate cognitive impairment (Mini Mental State ≤ 21)
  • body weight greater than 135 kg;
  • height more than 200 cm;
  • limb-length discrepancy greater than 2 cm;
  • presence of skin lesions on the trunk, pelvis and lower limbs that could interfere with the placement of the electrodes and straps anchoring the Lokomat.

Sites / Locations

  • HABILITARecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group

Control group

Arm Description

Participants received 25 sessions of robotically driven gait orthosis training on the Lokomat. Training occurred approximately 5 days/ week for 5 weeks, and each training session on the Lokomat lasted 30 minutes. All sessions were supervised by a trained research therapist. All participants started with 40% body weight-support and an initial treadmill speed of 1.5 km/h. Body weight-support was used primarily to facilitate an increase in walking speed; therefore, progression of training across subsequent sessions was standardized by preferentially increasing speed and then unloading body weight-support. Speed was increased to a range of 2.2 to 2.5 km/h before body weight-support was decreased. There was an active attempt to enhance the level of training at each session. After every Lokomat session, participants performed also 60 minutes of physiotherapy including general exercise program and a conventional gait training

Participants received 25 sessions of conventional physiotherapy. Training occurred approximately 5 days/week for 5 weeks, and each training session lasted 1 hour and half. Patients allocated to the Control Group performed the same conventional physiotherapy training of the other group: a general exercise program and a conventional gait training. The general exercise program consisted in cardiovascular warm-up exercises, muscle stretching exercises, active-assisted or active isometric and isotonic exercises for the main muscles of the trunk and limbs, relaxation exercises, coordination and static/dynamic balance exercises. The conventional gait therapy was based on the proprioceptive neuromuscular facilitation concept, training in walking on different surfaces with or without appropriate walking aids, exercises for the restoration of a correct gait pattern, implementation of residual compensatory strategies and progressive increase of walking resistance

Outcomes

Primary Outcome Measures

Timed 25 Foot Walk (25FW)
Assessment of gait performance in terms of speed. First component of the Multiple Sclerosis Functional Composite (MSCF) scale - leg function / ambulation, for the study and measurement of functional outcomes in clinical trials in patients with multiple sclerosis according to the "Task Force on Clinical Outcomes Assessment of the National Multiple Sclerosis Society "- 1994.

Secondary Outcome Measures

Timed 10 meter walking test (TWT)
Assessment of gait performance in terms of speed
6 minute walking test (6MWT)
Assessment of gait performance in terms of resistance
Tinetti Test (TT)
Assessment of balance and gait ability and the falls risk
Functional Ambulation Categories (FAC)
Assessment of ambulation ability
Modified Ashworth scale for lower limbs
Assessment of lower limbs spasticity
Modified Motricity Index for lower limbs
Assessment of lower limbs motor function
Knee extensor strength (KES)
Assessment of knee extensor strength by dynamometer measurement
Double Time Support (DST)
kinematic parameter corresponding to the duration of the double support phase of gait cycle, calculated as [ms /%]
Step Length Ratio (SLR)
kinematic parameter corresponding to gait symmetry, calculated as the ratio between the step length of both legs (shorter step length / longer step length)
Expanded Disability Status Scale (EDSS)
Traditionally used disability scale for multiple sclerosis
Functional Independence Measure (FIM)
Assessment of daily activities functional autonomy
Quality of Life Index (QL Index - SF36)
Measures of health-related quality of life
Numeric Rating Scale (NRS)
Assessment of pain

Full Information

First Posted
November 11, 2014
Last Updated
August 20, 2015
Sponsor
Habilita, Ospedale di Sarnico
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1. Study Identification

Unique Protocol Identification Number
NCT02291107
Brief Title
Robot-assisted Gait Training in Patients With Multiple Sclerosis: Efficacy and Comparison With Traditional Methods
Official Title
Robot-assisted Gait Training in Patients Affected by Multiple Sclerosis: Rehabilitative Efficacy Evaluation and Comparison With Traditional Methods
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
June 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Habilita, Ospedale di Sarnico

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In Multiple Sclerosis (MS) gait disorders represent one of the most disabling aspect that strongly influence patient quality of life. The improvement of walking ability is a primary goal for rehabilitation treatment. Current promising rehabilitative approaches for neurological disorders are based on the concept of the task-specific repetitive training. Hence, the interest in automated robotic devices that allow this typology of treatment for gait training. However, studies on the effectiveness of such methodologies are still poorly numerous in terms of functional improvement in MS patients. The aim of this controlled cross-over study is to evaluate the effectiveness of a Lokomat gait training in patients affected by Multiple Sclerosis in comparison to a ground conventional gait training.
Detailed Description
In Multiple Sclerosis (MS), the highly variable distribution of demyelinization areas and axonal loss in the Central Nervous System can lead to very complex and unpredictable neurological deficits and clinical patterns. Gait disorders as reduced speed and stride length, gait asymmetry, increased muscular energy expenditure, balance deficit and increased risk of falling, represent one of the most disabling aspect. These motor problems strongly influence the level of independence that a person affected by MS is able to achieve, resulting in severe negative impact on quality of life. Therefore, the improvement of walking ability is a primary goal for rehabilitation treatment. Many studies demonstrated that a conventional rehabilitation treatment based on physiotherapy could be effective in increasing muscle strength and motor function, improving gait and mobility abilities, reducing fatigue and risk of falls, leading finally to an overall increase of patient autonomy. According to the most recent neurophysiological concepts based on neural plasticity, in recent years the rehabilitative approaches that seem to be more effective in improving functional performance are based on the concept of the task-specific repetitive training. As in the case of the constraint induced movement therapy (CIMT) for upper limb rehabilitation and the body weight support treadmill training (BWSTT) for the lower, the factors that appear to positively affect patient outcome are the intensity, precocity, repeatability, specificity in a training that incorporates high numbers of repetitions of task-oriented practice. Hence, the interest in automated robotic devices for gait training for MS patients has grown. With their consistent, symmetrical lower-limb trajectories, robotic devices provide many of the proprioceptive inputs that may increase cortical activation and stimulation of Central Pattern Generator (CGPs) in order to improve motor function. The use of robot-assisted-gait-training (RAGT) allows: repetition of specific and stereotyped movements in order to acquire a correct and reproducible gait pattern in conditions of balance and symmetry, early start of treatment using the activity with body weight support, safeguard of the patient with reduction of fear of falling, in order to increase the quantity and quality of the performed exercise while minimizing the intervention of a therapist. However, studies on the effectiveness of such methodologies are still poorly numerous in terms of functional improvement in patients with MS. The aim of this controlled cross-over study is to evaluate the effectiveness of a robot-driven gait orthosis (Lokomat - Hocoma, Inc., Zurich, Switzerland) gait training in patients affected by Multiple Sclerosis in comparison to a ground conventional gait training. The improvement in gait pattern, motor ability and autonomy in the functional activities of daily living will be assessed by using validated clinical and functional scales and quantitative instrumental analysis of gait kinematic parameters

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Gait orthosis, Lokomat, Robotic Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
17 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Participants received 25 sessions of robotically driven gait orthosis training on the Lokomat. Training occurred approximately 5 days/ week for 5 weeks, and each training session on the Lokomat lasted 30 minutes. All sessions were supervised by a trained research therapist. All participants started with 40% body weight-support and an initial treadmill speed of 1.5 km/h. Body weight-support was used primarily to facilitate an increase in walking speed; therefore, progression of training across subsequent sessions was standardized by preferentially increasing speed and then unloading body weight-support. Speed was increased to a range of 2.2 to 2.5 km/h before body weight-support was decreased. There was an active attempt to enhance the level of training at each session. After every Lokomat session, participants performed also 60 minutes of physiotherapy including general exercise program and a conventional gait training
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Participants received 25 sessions of conventional physiotherapy. Training occurred approximately 5 days/week for 5 weeks, and each training session lasted 1 hour and half. Patients allocated to the Control Group performed the same conventional physiotherapy training of the other group: a general exercise program and a conventional gait training. The general exercise program consisted in cardiovascular warm-up exercises, muscle stretching exercises, active-assisted or active isometric and isotonic exercises for the main muscles of the trunk and limbs, relaxation exercises, coordination and static/dynamic balance exercises. The conventional gait therapy was based on the proprioceptive neuromuscular facilitation concept, training in walking on different surfaces with or without appropriate walking aids, exercises for the restoration of a correct gait pattern, implementation of residual compensatory strategies and progressive increase of walking resistance
Intervention Type
Device
Intervention Name(s)
Lokomat (Hocoma, Zurich, Switzerland)
Intervention Description
Patients allocated to the Experimental group performed a Robotic Assisted Gait Training by means of the Lokomat. The Lokomat is robotic device set up as an exoskeleton on the lower limbs of the patient. The system uses a dynamic body weight-support system to support he participant above a motorized treadmill synchronized with the Lokomat.
Intervention Type
Other
Intervention Name(s)
Conventional Physiotherapy
Intervention Description
Patients allocated to the Control Group performed a general exercise program and a conventional gait training. The same trained therapist treated all the patients in this group and standardized the duration of each part of the treatment.
Primary Outcome Measure Information:
Title
Timed 25 Foot Walk (25FW)
Description
Assessment of gait performance in terms of speed. First component of the Multiple Sclerosis Functional Composite (MSCF) scale - leg function / ambulation, for the study and measurement of functional outcomes in clinical trials in patients with multiple sclerosis according to the "Task Force on Clinical Outcomes Assessment of the National Multiple Sclerosis Society "- 1994.
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
Timed 10 meter walking test (TWT)
Description
Assessment of gait performance in terms of speed
Time Frame
5 weeks
Title
6 minute walking test (6MWT)
Description
Assessment of gait performance in terms of resistance
Time Frame
5 weeks
Title
Tinetti Test (TT)
Description
Assessment of balance and gait ability and the falls risk
Time Frame
5 weeks
Title
Functional Ambulation Categories (FAC)
Description
Assessment of ambulation ability
Time Frame
5 weeks
Title
Modified Ashworth scale for lower limbs
Description
Assessment of lower limbs spasticity
Time Frame
5 weeks
Title
Modified Motricity Index for lower limbs
Description
Assessment of lower limbs motor function
Time Frame
5 weeks
Title
Knee extensor strength (KES)
Description
Assessment of knee extensor strength by dynamometer measurement
Time Frame
5 weeks
Title
Double Time Support (DST)
Description
kinematic parameter corresponding to the duration of the double support phase of gait cycle, calculated as [ms /%]
Time Frame
5 weeks
Title
Step Length Ratio (SLR)
Description
kinematic parameter corresponding to gait symmetry, calculated as the ratio between the step length of both legs (shorter step length / longer step length)
Time Frame
5 weeks
Title
Expanded Disability Status Scale (EDSS)
Description
Traditionally used disability scale for multiple sclerosis
Time Frame
5 weeks
Title
Functional Independence Measure (FIM)
Description
Assessment of daily activities functional autonomy
Time Frame
5 weeks
Title
Quality of Life Index (QL Index - SF36)
Description
Measures of health-related quality of life
Time Frame
5 weeks
Title
Numeric Rating Scale (NRS)
Description
Assessment of pain
Time Frame
5 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of multiple sclerosis according to the McDonald's Criteria in stable phase of disease for at least 3 months. ability to walk 25 foot without assistance EDSS score between 3.5 and 7 Exclusion Criteria: exacerbations of the disease in the last 3 months deficits of somatic sensation involving the legs other neurological, orthopedic or cardiovascular co-morbility severe posture abnormalities severe-moderate cognitive impairment (Mini Mental State ≤ 21) body weight greater than 135 kg; height more than 200 cm; limb-length discrepancy greater than 2 cm; presence of skin lesions on the trunk, pelvis and lower limbs that could interfere with the placement of the electrodes and straps anchoring the Lokomat.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cristiano Sconza, MD
Phone
0354815515
Email
cristiano.sconza@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Umberto Bonassi, MD
Organizational Affiliation
HABILITA Zingonia
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Cristiano Sconza, MD
Organizational Affiliation
HABILITA Zingonia
Official's Role
Principal Investigator
Facility Information:
Facility Name
HABILITA
City
Zingonia di Ciserano
State/Province
Bergamo
ZIP/Postal Code
24040
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paola Sabattini
Phone
0354815515
Email
paolasabattini@habilita.it

12. IPD Sharing Statement

Citations:
PubMed Identifier
22146609
Citation
Schwartz I, Sajin A, Moreh E, Fisher I, Neeb M, Forest A, Vaknin-Dembinsky A, Karusis D, Meiner Z. Robot-assisted gait training in multiple sclerosis patients: a randomized trial. Mult Scler. 2012 Jun;18(6):881-90. doi: 10.1177/1352458511431075. Epub 2011 Dec 6.
Results Reference
result
PubMed Identifier
17942510
Citation
Beer S, Aschbacher B, Manoglou D, Gamper E, Kool J, Kesselring J. Robot-assisted gait training in multiple sclerosis: a pilot randomized trial. Mult Scler. 2008 Mar;14(2):231-6. doi: 10.1177/1352458507082358. Epub 2007 Oct 17.
Results Reference
result
PubMed Identifier
18971381
Citation
Lo AC, Triche EW. Improving gait in multiple sclerosis using robot-assisted, body weight supported treadmill training. Neurorehabil Neural Repair. 2008 Nov-Dec;22(6):661-71. doi: 10.1177/1545968308318473.
Results Reference
result
PubMed Identifier
22701177
Citation
Swinnen E, Beckwee D, Pinte D, Meeusen R, Baeyens JP, Kerckhofs E. Treadmill training in multiple sclerosis: can body weight support or robot assistance provide added value? A systematic review. Mult Scler Int. 2012;2012:240274. doi: 10.1155/2012/240274. Epub 2012 May 30.
Results Reference
result
PubMed Identifier
22140197
Citation
Vaney C, Gattlen B, Lugon-Moulin V, Meichtry A, Hausammann R, Foinant D, Anchisi-Bellwald AM, Palaci C, Hilfiker R. Robotic-assisted step training (lokomat) not superior to equal intensity of over-ground rehabilitation in patients with multiple sclerosis. Neurorehabil Neural Repair. 2012 Mar-Apr;26(3):212-21. doi: 10.1177/1545968311425923. Epub 2011 Dec 2.
Results Reference
result
PubMed Identifier
21674396
Citation
Wier LM, Hatcher MS, Triche EW, Lo AC. Effect of robot-assisted versus conventional body-weight-supported treadmill training on quality of life for people with multiple sclerosis. J Rehabil Res Dev. 2011;48(4):483-92. doi: 10.1682/jrrd.2010.03.0035.
Results Reference
result
PubMed Identifier
21187202
Citation
Pilutti LA, Lelli DA, Paulseth JE, Crome M, Jiang S, Rathbone MP, Hicks AL. Effects of 12 weeks of supported treadmill training on functional ability and quality of life in progressive multiple sclerosis: a pilot study. Arch Phys Med Rehabil. 2011 Jan;92(1):31-6. doi: 10.1016/j.apmr.2010.08.027.
Results Reference
result
PubMed Identifier
17450642
Citation
Giesser B, Beres-Jones J, Budovitch A, Herlihy E, Harkema S. Locomotor training using body weight support on a treadmill improves mobility in persons with multiple sclerosis: a pilot study. Mult Scler. 2007 Mar;13(2):224-31. doi: 10.1177/1352458506070663.
Results Reference
result
PubMed Identifier
12732691
Citation
Eng J. Sample size estimation: how many individuals should be studied? Radiology. 2003 May;227(2):309-13. doi: 10.1148/radiol.2272012051.
Results Reference
result

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Robot-assisted Gait Training in Patients With Multiple Sclerosis: Efficacy and Comparison With Traditional Methods

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