Lokomat Training Effects on MS Gait Abnormalities
Primary Purpose
Multiple Sclerosis
Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Lokomat
Sponsored by

About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring Rehabilitation, Treadmill, MS, Gait, Robot
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of MS by McDonald criteria
- Ability to clearly understand written and oral direction in English
- Self-reported gait problem
- One or more falls in the past 6 months
- The ability to walk 25 feet with no more than a cane for assistance (The subject must be comfortable using a cane)
- Age 18-70
- Written informed consent to participate in the study
- Approval from subject's primary care physician for physical activity
Exclusion Criteria:
- No relapse within the last 3 months
- No more than two relapses within the past 12 months
- Recent myocardial infarction
- Uncontrolled hypertension or diabetes
- Symptomatic fall in blood pressure when standing
- Vascular claudication or pitting edema
- Cognitive impairments that limit comprehension of protocol instructions (assessed by Comprehension Test of Consent Form)
- Body weight over 150 kg
- FES-I < 25
- Lower extremity injuries that limit range of motion or function
- Joint problems (hip or leg) that limit range of motion or cause pain with movement
- Unstable fractures
- Pressure sores with any skin breakdown in areas in contact with the body harness or the robot-driven gait orthotic apparatus
- Currently enrolled in an alcohol or drug treatment program
- A complicating medical condition that would prevent completion of the trial
- Enrolled in or planning to enroll in another interventional research trial using procedures proposed to enhance or limit the function of the upper or lower extremities (such as adjuvant rehabilitation or Botox injections) during the 24 weeks of participation
- A difference of more than 2cm between subjects' right and left leg lengths
- Unable to be properly fit into the harness or Lokomat device
- Hypertonicity or spasticity that it interferes with a proper fit into the Lokomat
- Pregnancy at enrollment, as determined by a home pregnancy test kit at screening visit
Sites / Locations
- Providence VA Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Arm 1
Arm Description
Body-weight supported treadmill training
Outcomes
Primary Outcome Measures
Frequency of Falls
Secondary Outcome Measures
Full Information
NCT ID
NCT00766272
First Posted
October 2, 2008
Last Updated
September 19, 2013
Sponsor
US Department of Veterans Affairs
1. Study Identification
Unique Protocol Identification Number
NCT00766272
Brief Title
Lokomat Training Effects on MS Gait Abnormalities
Official Title
Gait Rehabilitation for Multiple Sclerosis Using Robot-assisted Body-weight-supported Treadmill Training (Lokomat)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2013
Overall Recruitment Status
Terminated
Why Stopped
Study re-designed
Study Start Date
June 2008 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Multiple sclerosis is a degenerative disease that affects more than 400,000 people in the US alone. MS is in fact the most common disabling neurological disorder in young adults. Symptoms of the disease can include problems with balance, walking, fatigue, weakness and vision. Over 85% of people with Multiple Sclerosis have problems walking. This can cause them to fall or have a constant fear of falling. To prevent falling, MS patients rely on equipment, such as walkers and canes. These costs can cause financial difficulties for MS patients and families.
A significant problem that is only recently being studied is the relationship between falling and MS. Recent studies have shown that MS patients fall more often than those without MS, and also fall more than the elderly population. The consequent fear of falling is also an important problem, as those worried about falling will probably change their daily habits to lower their risk. This can mean keeping from certain physical and social activities or even staying indoors. Thus, falls and fear of falling can have negative medical, physical, psychological, and social consequences for the patient.
Improving patients' walking may help reduce falls and the fear of falling. Treadmill training has been shown to improve walking in patients with MS and to lower their risk of falling. One way to train patients on a treadmill is with the use of robots that can help move their limbs in a more normal way. This kind of robot-assisted treadmill training may provide even greater benefits than treadmill training alone.
The study is expected to last 6-7.5 months. One group of participants will receive weekly telephone calls and will be asked questions on other physical activities, falls, and activity limitations the patient had during the week. Participants assigned to robot-assisted treadmill training will receive twice weekly training session for 8 weeks, for a total of 16 sessions. Each session will last about 65 to 90 minutes.
The goal of this study is to see if robot-assisted treadmill training will reduce falls and fear of falling in patients with MS. Robot-assisted treadmill training has been shown to be effective in reducing falls and fear of falling in Parkinson's disease patients. This type of training has not been tested in patients with Multiple Sclerosis. The proposed study will help to address this gap and also provide additional data on other possible improvements due to robot-assisted treadmill training including ambulation, social participation, fatigue, and balance.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Rehabilitation, Treadmill, MS, Gait, Robot
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Body-weight supported treadmill training
Intervention Type
Device
Intervention Name(s)
Lokomat
Intervention Description
Body-weight will be supported using a harness, which suspends the subject above a motorized treadmill (Lokomat, Hocoma, Zurich, Switzerland). The system also incorporates a robot-driven gait orthotic, called the Lokomat, which will be secured to the subject's lower extremity and pelvis using adjustable cuffs and pads. The Lokomat uses computer-controlled motors to drive the hips and knees toward more normative kinematic patterns for gait.
Primary Outcome Measure Information:
Title
Frequency of Falls
Time Frame
6-7.5 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:
Diagnosis of MS by McDonald criteria
Ability to clearly understand written and oral direction in English
Self-reported gait problem
One or more falls in the past 6 months
The ability to walk 25 feet with no more than a cane for assistance (The subject must be comfortable using a cane)
Age 18-70
Written informed consent to participate in the study
Approval from subject's primary care physician for physical activity
Exclusion Criteria:
No relapse within the last 3 months
No more than two relapses within the past 12 months
Recent myocardial infarction
Uncontrolled hypertension or diabetes
Symptomatic fall in blood pressure when standing
Vascular claudication or pitting edema
Cognitive impairments that limit comprehension of protocol instructions (assessed by Comprehension Test of Consent Form)
Body weight over 150 kg
FES-I < 25
Lower extremity injuries that limit range of motion or function
Joint problems (hip or leg) that limit range of motion or cause pain with movement
Unstable fractures
Pressure sores with any skin breakdown in areas in contact with the body harness or the robot-driven gait orthotic apparatus
Currently enrolled in an alcohol or drug treatment program
A complicating medical condition that would prevent completion of the trial
Enrolled in or planning to enroll in another interventional research trial using procedures proposed to enhance or limit the function of the upper or lower extremities (such as adjuvant rehabilitation or Botox injections) during the 24 weeks of participation
A difference of more than 2cm between subjects' right and left leg lengths
Unable to be properly fit into the harness or Lokomat device
Hypertonicity or spasticity that it interferes with a proper fit into the Lokomat
Pregnancy at enrollment, as determined by a home pregnancy test kit at screening visit
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Albert Lo, MD PhD
Organizational Affiliation
Providence VA Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Providence VA Medical Center
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02908-4799
Country
United States
12. IPD Sharing Statement
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Lokomat Training Effects on MS Gait Abnormalities
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