- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02291107
Robot-assisted Gait Training in Patients With Multiple Sclerosis: Efficacy and Comparison With Traditional Methods
August 20, 2015 updated by: Dr. Cristiano Sconza, Habilita, Ospedale di Sarnico
Robot-assisted Gait Training in Patients Affected by Multiple Sclerosis: Rehabilitative Efficacy Evaluation and Comparison With Traditional Methods
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.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
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
Study Type
Interventional
Enrollment (Anticipated)
17
Phase
- Not Applicable
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
-
-
Bergamo
-
Zingonia di Ciserano, Bergamo, Italy, 24040
- Recruiting
- HABILITA
-
Contact:
- Paola Sabattini
- Phone Number: 0354815515
- Email: paolasabattini@habilita.it
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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.
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: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
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
|
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.
|
|
Active Comparator: Control group
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
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Timed 25 Foot Walk (25FW)
Time Frame: 5 weeks
|
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.
|
5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Timed 10 meter walking test (TWT)
Time Frame: 5 weeks
|
Assessment of gait performance in terms of speed
|
5 weeks
|
|
6 minute walking test (6MWT)
Time Frame: 5 weeks
|
Assessment of gait performance in terms of resistance
|
5 weeks
|
|
Tinetti Test (TT)
Time Frame: 5 weeks
|
Assessment of balance and gait ability and the falls risk
|
5 weeks
|
|
Functional Ambulation Categories (FAC)
Time Frame: 5 weeks
|
Assessment of ambulation ability
|
5 weeks
|
|
Modified Ashworth scale for lower limbs
Time Frame: 5 weeks
|
Assessment of lower limbs spasticity
|
5 weeks
|
|
Modified Motricity Index for lower limbs
Time Frame: 5 weeks
|
Assessment of lower limbs motor function
|
5 weeks
|
|
Knee extensor strength (KES)
Time Frame: 5 weeks
|
Assessment of knee extensor strength by dynamometer measurement
|
5 weeks
|
|
Double Time Support (DST)
Time Frame: 5 weeks
|
kinematic parameter corresponding to the duration of the double support phase of gait cycle, calculated as [ms /%]
|
5 weeks
|
|
Step Length Ratio (SLR)
Time Frame: 5 weeks
|
kinematic parameter corresponding to gait symmetry, calculated as the ratio between the step length of both legs (shorter step length / longer step length)
|
5 weeks
|
|
Expanded Disability Status Scale (EDSS)
Time Frame: 5 weeks
|
Traditionally used disability scale for multiple sclerosis
|
5 weeks
|
|
Functional Independence Measure (FIM)
Time Frame: 5 weeks
|
Assessment of daily activities functional autonomy
|
5 weeks
|
|
Quality of Life Index (QL Index - SF36)
Time Frame: 5 weeks
|
Measures of health-related quality of life
|
5 weeks
|
|
Numeric Rating Scale (NRS)
Time Frame: 5 weeks
|
Assessment of pain
|
5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Umberto Bonassi, MD, Habilita Zingonia
- Principal Investigator: Cristiano Sconza, MD, Habilita Zingonia
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Eng J. Sample size estimation: how many individuals should be studied? Radiology. 2003 May;227(2):309-13. doi: 10.1148/radiol.2272012051.
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
June 1, 2014
Primary Completion (Anticipated)
December 1, 2015
Study Completion (Anticipated)
June 1, 2016
Study Registration Dates
First Submitted
November 11, 2014
First Submitted That Met QC Criteria
November 13, 2014
First Posted (Estimate)
November 14, 2014
Study Record Updates
Last Update Posted (Estimate)
August 21, 2015
Last Update Submitted That Met QC Criteria
August 20, 2015
Last Verified
August 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- LK.S P07
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.
Clinical Trials on Multiple Sclerosis
-
University Hospital, Basel, SwitzerlandSwiss National Science FoundationRecruitingMultiple Sclerosis (MS) | Relapsing-remitting Multiple Sclerosis (RRMS) | Secondary-progressive Multiple Sclerosis (SPMS) | Primary Progressive Multiple Sclerosis (PPMS)Switzerland
-
University of California, Los AngelesUnknownRelapsing-remitting Multiple Sclerosis | Secondary-progressive Multiple Sclerosis | Primary-progressive Multiple SclerosisUnited States
-
BiogenCompletedMultiple Sclerosis | Relapsing-Remitting Multiple Sclerosis | Secondary Progressive Multiple Sclerosis | Multiple Sclerosis, Primary Progressive | Multiple Sclerosis, Remittent ProgressiveJapan
-
Cabaletta BioNot yet recruitingProgressive Multiple Sclerosis | Multiple Sclerosis | Multiple Sclerosis (Relapsing Remitting) | Relapsing Multiple Sclerosis (RMS) | Progressive Multiple Sclerosis (PMS) | Multiple Sclerosis (MS) - Relapsing-remitting | Multiple Sclerosis - Relapsing Remitting
-
Rigshospitalet, DenmarkOdense University Hospital; Aarhus University Hospital; Hvidovre University Hospital and other collaboratorsActive, not recruitingRelapsing Remitting Multiple Sclerosis | Primary Progressive Multiple Sclerosis | Secondary Progressive Multiple SclerosisDenmark
-
The Cleveland ClinicUniversity Hospitals Cleveland Medical CenterCompletedRelapsing-Remitting Multiple Sclerosis | Secondary Progressive Multiple Sclerosis | Progressive Relapsing Multiple SclerosisUnited States
-
Icahn School of Medicine at Mount SinaiColumbia University; New York Stem Cell Foundation Research InstituteCompletedClinically Isolated Syndrome | Relapsing-Remitting Multiple Sclerosis | Primary Progressive Multiple Sclerosis | Secondary Progressive Multiple SclerosisUnited States
-
Novartis PharmaceuticalsCompletedRelapsing-remitting Multiple Sclerosis | Active Secondary Progressive Multiple SclerosisJapan
-
Banc de Sang i TeixitsVall d'Hebron Research Institute (VHIR)CompletedRelapsing-Remitting Multiple Sclerosis | Secondary Progressive Multiple SclerosisSpain
-
BiogenElan PharmaceuticalsCompletedRelapsing-Remitting Multiple Sclerosis | Secondary Progressive Multiple SclerosisUnited States
Clinical Trials on Lokomat (Hocoma, Zurich, Switzerland)
-
University of WinchesterHampshire Hospitals NHS Foundation Trust; University Hospitals Dorset NHS Foundation...Recruiting
-
Habilita, Ospedale di SarnicoUnknown
-
University of Sao Paulo General HospitalCompletedSpinal Cord InjuryBrazil
-
University Hospital of FerraraUniversita di Verona; Università degli Studi di FerraraRecruiting
-
University Hospital of FerraraAzienda Ospedaliero, Universitaria PisanaCompleted
-
University of ZurichCompletedSpinal Cord InjuriesSwitzerland, Spain, Germany
-
Bern University of Applied SciencesSwiss Federal Institute of Technology; Maastricht University; Reha RheinfeldenCompletedCardiovascular Diseases | StrokeSwitzerland
-
Kowloon Hospital, Hong KongThe Hong Kong Polytechnic UniversityCompleted
-
Spaulding Rehabilitation HospitalTerminated
-
Swiss Federal Institute of TechnologyZuercher Hoehenklinik Wald; Hocoma AG, SwitzerlandCompletedStroke | Spinal Cord InjurySwitzerland