Lokomat Training Effects on MS Gait Abnormalities

NCT ID: NCT00766272

Last Updated: 2013-09-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-06-30
• Study Completion Date: 2008-06-30

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.

Conditions

Multiple Sclerosis

Keywords

Rehabilitation; Treadmill; MS; Gait; Robot

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Arm 1

Body-weight supported treadmill training

Group Type: EXPERIMENTAL

Lokomat

Intervention Type: DEVICE

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.

Interventions

Lokomat

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.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Diagnosis of MS by McDonald criteria

2. Ability to clearly understand written and oral direction in English

3. Self-reported gait problem

4. One or more falls in the past 6 months

5. The ability to walk 25 feet with no more than a cane for assistance (The subject must be comfortable using a cane)

6. Age 18-70

7. Written informed consent to participate in the study

8. Approval from subject's primary care physician for physical activity

Exclusion Criteria

1. No relapse within the last 3 months

2. No more than two relapses within the past 12 months

3. Recent myocardial infarction

4. Uncontrolled hypertension or diabetes

5. Symptomatic fall in blood pressure when standing

6. Vascular claudication or pitting edema

7. Cognitive impairments that limit comprehension of protocol instructions (assessed by Comprehension Test of Consent Form)

8. Body weight over 150 kg

9. FES-I < 25

10. Lower extremity injuries that limit range of motion or function

11. Joint problems (hip or leg) that limit range of motion or cause pain with movement

12. Unstable fractures

13. Pressure sores with any skin breakdown in areas in contact with the body harness or the robot-driven gait orthotic apparatus

14. Currently enrolled in an alcohol or drug treatment program

15. A complicating medical condition that would prevent completion of the trial

16. 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

17. A difference of more than 2cm between subjects' right and left leg lengths

18. Unable to be properly fit into the harness or Lokomat device

19. Hypertonicity or spasticity that it interferes with a proper fit into the Lokomat

20. Pregnancy at enrollment, as determined by a home pregnancy test kit at screening visit

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

US Department of Veterans Affairs

FED

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Albert Lo, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Providence VA Medical Center

Locations

Providence VA Medical Center

Providence, Rhode Island, United States

Countries

United States

Other Identifiers

LO-0003

Identifier Type: -

Identifier Source: org_study_id