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Lokomat Treadmill Training Effects on MS Gait

Primary Purpose

Gait, Unsteady, Multiple Sclerosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Body-weight supported treadmill training +/- Lokomat assistance
Usual Care - no active intervention
Sponsored by
Mount Sinai Rehabilitation Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gait, Unsteady focused on measuring Multiple Sclerosis, gait, falls, lokomat, body-weight support treadmill training

Eligibility Criteria

25 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Main Inclusion Criteria:

  • Clinical diagnosis of MS
  • EDSS level between 3.5-6.0
  • Problems with ambulation
  • able to ambulate 25 feet without an assistive device

Main Exclusion Criteria:

  • Lower extremity injuries that limit range of motion or function
  • Unable to demonstrate an understanding of the process of the study and or fully understand instructions in order to safely participate in the study and use study equipment
  • Body weight over 150 kg

    • complete inclusion/exclusion criteria listed in consent form

Sites / Locations

  • Mandell Center for Multiple Sclerosis at Mt. Sinai Rehabilitation Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control group

Combination Treadmill training group

Arm Description

The placebo group did not receive treatment during the matched period yet did undergo all assessments. The MS Placebo group received equal treatment following the study intervention period.

Subjects randomized to Combination therapy received 20 minutes of Lokomat assisted treadmill training followed by up to 20 minutes of BWS treadmill training (without robotic assistance) twice a week.

Outcomes

Primary Outcome Measures

Gait Parameters

Secondary Outcome Measures

Full Information

First Posted
February 3, 2009
Last Updated
November 9, 2015
Sponsor
Mount Sinai Rehabilitation Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00835835
Brief Title
Lokomat Treadmill Training Effects on MS Gait
Official Title
Lokomat Treadmill Training Effects on MS Gait
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
February 2008 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mount Sinai Rehabilitation Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is being done to test the possible benefits of gait-specific training using body-weight supported, Lokomat assisted, treadmill training in people with Multiple Sclerosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gait, Unsteady, Multiple Sclerosis
Keywords
Multiple Sclerosis, gait, falls, lokomat, body-weight support treadmill training

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
The placebo group did not receive treatment during the matched period yet did undergo all assessments. The MS Placebo group received equal treatment following the study intervention period.
Arm Title
Combination Treadmill training group
Arm Type
Experimental
Arm Description
Subjects randomized to Combination therapy received 20 minutes of Lokomat assisted treadmill training followed by up to 20 minutes of BWS treadmill training (without robotic assistance) twice a week.
Intervention Type
Other
Intervention Name(s)
Body-weight supported treadmill training +/- Lokomat assistance
Other Intervention Name(s)
Lokomat
Intervention Description
walking
Intervention Type
Other
Intervention Name(s)
Usual Care - no active intervention
Other Intervention Name(s)
control group
Intervention Description
No treatment used for comparison
Primary Outcome Measure Information:
Title
Gait Parameters
Time Frame
Baseline, throughout study enrollment and 2 months follow-up
Other Pre-specified Outcome Measures:
Title
6 minute walk
Description
The 6 minute walk test is measured on a treadmill. The subject is asked to indicate the most comfortable treadmill speed to the therapist. The subject is instructed to walk as far as possible in 6 minutes and the total distance covered in 6 minutes is recorded. A harness, without body-weight support, is attached for safety.
Time Frame
Baseline, throughout study enrollment and 2 months follow-up
Title
MSQLI (Multiple Sclerosis Quality of Life Index)
Description
The MSQLI is a battery consisting of 10 individual scales providing a quality of life measure that is both generic and MS-specific (Fischer et al, 1999). The MS quality of life index is a validated instrument used in accessing multiple aspects of quality of life for persons with MS. It is a modification of the short-form health survey (SF-36) and requires about 30-45 minutes to complete.
Time Frame
Baseline, throughout study enrollment and 2 months follow-up
Title
Timed 25-foot walk
Description
Will be collected over-ground and on a straight 25-foot GaitRite electronic mat. The subject will be timed over the 25-foot distance both at their self-designated usual pace and at the fastest safe pace possible. Data will be collected using a laptop computer. The GaitRite system has software to calculate several measures including velocity, stride length, base width and number of steps.
Time Frame
Baseline, throughout study enrollment and 2 months follow-up
Title
Frequency of Falls
Description
Falls will be recorded by the subjects onto a "Falls Calender" provided to the subjects. Subjects will be given the following definition of a fall: "an event which results in a person coming to rest inadvertently on the ground or other lower level, and other than as a consequence of the following: sustaining a violent blow; loss of consciousness; sudden onset of paralysis, as in a stroke and an epileptic seizure" (Vellas 1992).
Time Frame
Baseline, throughout study enrollment and 2 months follow-up
Title
FRT (Functional Reach Test)
Description
The Functional Reach test is a measure of balance and is the difference from arm's length and maximal forward reach. The support case is fixed. The test utilizes a 48-inch measuring device or "yardstick" for measuring functional reach. Data is measured in inches (Duncan P. W. et al 1990).
Time Frame
Baseline, throughout study enrollment and 2 months follow-up
Title
CDP (Computerized Dynamic Posturography)
Description
NeuroCom Smart Balance Master system. The use of CDP has allowed clinicians to objectively measure the postural components of balance (Liston 1996). CDP assesses sway by measuring shifts in the center of gravity (COG) as a person moves within the available limits of stability (LOS). Two types of tests will be used with CDP; they are the Sensory Organization Test (SOT) and the LOS test. SOT: measures sway and is designed to quantify an individual's ability to maintain balance in a variety of complex sensory conditions. LOS: measures volitional control of the COG. Test measures include maximum end-point excursion for anterior, posterior, right, and left movements.
Time Frame
Baseline, throughout study enrollment and 2 months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Main Inclusion Criteria: Clinical diagnosis of MS EDSS level between 3.5-6.0 Problems with ambulation able to ambulate 25 feet without an assistive device Main Exclusion Criteria: Lower extremity injuries that limit range of motion or function Unable to demonstrate an understanding of the process of the study and or fully understand instructions in order to safely participate in the study and use study equipment Body weight over 150 kg complete inclusion/exclusion criteria listed in consent form
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Albert Lo, MD, PhD
Organizational Affiliation
Mandell Center for Multiple Sclerosis at Mount Sinai Rehabilitation Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mandell Center for Multiple Sclerosis at Mt. Sinai Rehabilitation Hospital
City
Hartford
State/Province
Connecticut
ZIP/Postal Code
06112
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
10467384
Citation
Fischer JS, LaRocca NG, Miller DM, Ritvo PG, Andrews H, Paty D. Recent developments in the assessment of quality of life in multiple sclerosis (MS). Mult Scler. 1999 Aug;5(4):251-9. doi: 10.1177/135245859900500410.
Results Reference
background
PubMed Identifier
1591453
Citation
Vellas B, Baumgartner RN, Wayne SJ, Conceicao J, Lafont C, Albarede JL, Garry PJ. Relationship between malnutrition and falls in the elderly. Nutrition. 1992 Mar-Apr;8(2):105-8.
Results Reference
background
PubMed Identifier
2229941
Citation
Duncan PW, Weiner DK, Chandler J, Studenski S. Functional reach: a new clinical measure of balance. J Gerontol. 1990 Nov;45(6):M192-7. doi: 10.1093/geronj/45.6.m192.
Results Reference
background
PubMed Identifier
8629916
Citation
Liston RA, Brouwer BJ. Reliability and validity of measures obtained from stroke patients using the Balance Master. Arch Phys Med Rehabil. 1996 May;77(5):425-30. doi: 10.1016/s0003-9993(96)90028-3.
Results Reference
background
Links:
URL
http://www.saintfrancisdoctors.com/ms
Description
Mandell Center for Multiple Sclerosis home page

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Lokomat Treadmill Training Effects on MS Gait

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