Functional and Physiological Responses to Lokomat Therapy (Pilot Study)

NCT ID: NCT00883142

Last Updated: 2013-06-11

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 27 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2006-10-31
• Study Completion Date: 2013-03-31

Brief Summary

Individuals with neurological deficiencies such as those who have spinal cord injury, stroke, traumatic brain injury, Parkinson's disease, and multiple sclerosis often lose their ability to ambulate over ground. Loss of functional mobility not only impedes everyday life, but may also affect many systems and organs in the body. The investigators are interested in obtaining a wide variety of data in order to obtain a better understanding of changes that occur as a result of receiving Lokomat therapy. The investigators will be studying body composition, cardiac, pulmonary, endocrine, metabolic, and molecular changes after a 12-week clinical therapy program.

Detailed Description

Description of the Clinical Lokomat Therapy program:

This is a 12-week program with 3 to 5 sessions per week. Each session includes: 15-20 minutes of patient set-up (set-up time becomes about 5 to 10 minutes after a few sessions), 5-10 minutes of warm-up, 20-40 minutes of Lokomat therapy, 5-10 minutes of cool-down, and 5-10 minutes to remove the patient from the system. During the Lokomat sessions, heart rate and blood pressure are monitored by the therapist and recorded. Work performed is measured and recorded in the Lokomat computer for time, speed, amount of weight bearing, and distance.

Description of the Research Component:

A pre and post, prospective study design will be employed. Baseline measurements (Please see below and Table 1 for detailed descriptions) will be performed prior to start of the Lokomat therapy program and then again after completion of the 12-week program. A chart review will be performed at baseline only for documentation of medical history and medications. In a subset of patients a muscle biopsy will be performed for gene expression at baseline and week 12.

As part of Clinical Care, during each of the Lokomat therapy sessions the following information is collected:

1. Work (total time, speed, distance, amount of weight bearing)

2. Heart rate (HR)

3. Blood Pressure (SBP, DBP)

4. Perception of exertion (Borg Scale)

5. Lipid profile (pre and post)

6. Albumin (pre and post)

For Research purposes the following is being proposed:

Review and record work, HR, BP, Borg Scale from all clinical sessions

Baseline and Week 12 measurements (performed on a separate days or prior to the sessions):

1. Resting energy expenditure (REE)

2. Body Composition [dual energy x-ray absorptiometry (DEXA) ) - [scans include total body, dual femur, and the knee], partial body potassium counting (PBKleg), bioelectrical impedance analysis (BIA), anthropometric and skin fold measurements]

3. Fasting blood draw for plasma glucose and insulin (FPG, FPI), lipid profile, testosterone, sex hormone binding globulin (SHBG), insulin-like growth factor 1 (IGF-1), bone markers, coagulation factors, platelet aggregation, 2 hour standard oral glucose tolerance testing (OGTT) with insulin levels.

4. Autonomic and blood pressure regulation studies [resting and tilt table provocation, for heart rate and blood pressure variability (HRV, BPV), arterial blood flow, and venous occlusion]

5. Disability-specific quality of life (QOL) and activities of daily living surveys [GI-Bowel survey, brief pain inventory (BPI), fatigue survey, spasticity scale, mini mental status exam (MMSE)]. These disease-specific QOLs will include the question "How do you rate your general health and well-being over the past week?" A Lickert scale response will be incorporated.

6. Functional Mobility Assessment

7. Muscle biopsy for gene expression (subset of patients only).

Conditions

Spinal Cord Injuries; Multiple Sclerosis; Stroke

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Group 1

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

1. Patients will have been evaluated on the Rehabilitation Service for entry into the clinical therapy program.

2. Any patient who is already eligible for Lokomat therapy is a candidate for this research project.

Exclusion Criteria

1. Pregnant women

2. History of fractures of the lower extremities

3. Bone density study indicating bone loss greater than 5 standard deviations from normal.

4. Fixed contractures of the ankles, knees or hips

5. Uncontrolled spasticity that significantly interferes with movement of lower extremities.

6. Uncooperative, unmotivated patients or patients whom cannot follow instructions on a consistent basis or communicate effectively with the treating clinicians.

7. Pressure ulcers over the greater trochanters, ischial tuberosities and sacrum.

8. Weight greater than 250 lbs

9. severe orthostatic hypotension (drop in blood pressure more than 30mm Hg when moving from sitting to standing posture)

10. Acute medical illness (i.e. infection)

11. Recently documented DVT in lower extremities

12. SCI ASIA's A and B

• Minimum Eligible Age: 18 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

Ann M. Spungen, EdD

Role: PRINCIPAL_INVESTIGATOR

VA Medical Center, Bronx

Locations

VA Medical Center, Bronx

The Bronx, New York, United States

Countries

United States

Other Identifiers

B4162C-11

Identifier Type: -

Identifier Source: org_study_id