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Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury

Primary Purpose

Spinal Cord Injury

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Lokomat treadmill training
Aquatic exercise therapy
Sponsored by
University of Maryland, Baltimore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injury focused on measuring robotic weight support, aquatic exercise, incomplete motor spinal cord injury, ASIA C and D

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-65 years
  • Level of injury between C4 and T12 based on ASIA classification
  • Chronic (greater than 12 months) spinal injury
  • Completion of all conventional inpatient rehabilitation therapy
  • Motor incomplete spinal cord injury (AIS C or D)
  • Competency to provide informed consent
  • Ability to tolerate a standing frame for at least 30 minutes

Exclusion Criteria:

  • Currently performing aquatic therapy or Lokomat training as part of clinical care
  • Complete or concurrent lower motor neuron injury as defined by the absence of reflexes bilaterally at the knees and the ankles
  • Uncontrolled seizures
  • Skin opening greater than 2 cm in diameter
  • Alcohol consumption > 3 oz liquor, or 3 x 4oz of wine, or 36 oz of beer per day
  • Cardiac history of (a) unstable angina, (b) recent (< 3 months) myocardial infarction, (c) congestive heart failure (NYHA category II), or (d) hemodynamically significant valvular dysfunction
  • Medical history of (a) recent hospitalization for severe disease or surgery, (b)undiagnosed diabetics (fasting glucose > 120) or poorly controlled diabetics (those not on a stable regimen for >6 months) unable to be controlled with medical treatment, (c) significant orthopedic or chronic pain conditions limiting exercise, (d) active neoplastic disease, (e) pulmonary or renal disease, and (f) presence of any serious medical condition with a prognosis for death or dependency in the next 2 months
  • History of long bone fracture in the legs
  • Frequent bouts of autonomic dysreflexia (as determined by the principal investigator)
  • Any other medical co-morbidities that based on the judgment of the local principal investigator would preclude safe participation in the study

Sites / Locations

  • Shepherd Center, Virginia C. Crawford Research Institute
  • University of Maryland Rehabilitation & Orthopaedic Institute (formerly known as Kernan Hospital)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Lokomat Training

Aquatic Therapy

Arm Description

Lokomat robotic assisted treadmill training Lokomat Treadmill Training

Aquatic exercise therapy

Outcomes

Primary Outcome Measures

Number of Participants Demonstrating 10% Change: Arm Ergometer and Lokomat Metabolic Cart VO2 Peak
Peak VO2 via Arm Ergometer and Lokomat with metabolic cart

Secondary Outcome Measures

Number of Movement Recorded by Activity Monitor (SAM)
SAM movements not just steps were gathered one time pre, crossover and post and worn on ankle for 5 days; percent change for each intervention

Full Information

First Posted
July 12, 2011
Last Updated
May 6, 2021
Sponsor
University of Maryland, Baltimore
Collaborators
Shepherd Center, Atlanta GA
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1. Study Identification

Unique Protocol Identification Number
NCT01407354
Brief Title
Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury
Official Title
Lokomat and Aquatic Therapy in Chronic Motor Incomplete Spinal Cord Injury
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Maryland, Baltimore
Collaborators
Shepherd Center, Atlanta GA

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Many people with spinal cord injury (SCI) hold some ability to move their leg muscles, and are therefore considered to demonstrate a motor incomplete injury. After such a spinal cord injury, individuals are able to walk less both in their home and in their community. De-conditioning, or a lack of endurance and fitness also occurs. Several methods are available to try to improve walking ability and the fitness of persons with motor incomplete spinal cord injury. This study examines two of these methods. The first is the use of robotically assisted body-weight supported walking using a device called the Lokomat. The second is aquatic or pool-based exercise. The investigators are researching the impact of these two techniques on walking ability and fitness in people who experienced motor incomplete spinal cord injury for at least 12 months.
Detailed Description
This research will occur in two centers Kernan Orthopedics and Rehabilitation Hospital in Baltimore, Maryland and Shepherd Center in Atlanta, Georgia. A total of 36 volunteers over a three year period are needed. In order to qualify for this study, individuals must be 18 to 65 years old with a motor incomplete SCI. The level of injury can range from the fourth cervical level in the neck to the twelfth thoracic level in the back. Potential volunteers must be able to tolerate standing in a standing frame for at least 30 minutes. Individuals will be assessed by a physician to determine their eligibility for the study and if participating in this type of exercise would be safe. Participants must be able to understand the study requirements and sign an informed consent document. Participants will need to commit to a total of seven months. Included in this time is: testing, then the 3 months of exercise, testing, 2 week break, then the second 3 months of exercise, and a final testing. Half of the group will start with the Lokomat training and half will start wtih aquatic exercise. Each group will then switch to the other exercise condition. Exercise sessions will occur three times per week and last approximately 45-55 minutes. A physical therapist will provide personal direction for each of the exercise groups. Walking ability and cardiovascular fitness, as well as muscle strength will be assessed before starting exercise, at the three-month point and then at the six month point. It is hoped that that this type of exercise therapy will help individuals with motor incomplete spinal injury both walk better and experience better heart-lung fitness and endurance. The risks associated with this type of study are similar to any type of cardiovascular exercise. In addition, individuals with spinal cord injury may present with some medical conditions, there may be other risks of the study. The physicians and therapists involved in the research will discuss these risks in detail with the individuals who enroll. This type of research is important to better understand how best to prescribe exercise treatments to people with spinal injury. This is especially true with regards to aquatic therapy, since there is very little scientific data on its effect in this group of individuals. The rigorous assessment of aquatic exercise, which is already available in many communities, may expand the fitness opportunities for individuals with incomplete spinal cord injury.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
Keywords
robotic weight support, aquatic exercise, incomplete motor spinal cord injury, ASIA C and D

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Lokomat Training
Arm Type
Experimental
Arm Description
Lokomat robotic assisted treadmill training Lokomat Treadmill Training
Arm Title
Aquatic Therapy
Arm Type
Active Comparator
Arm Description
Aquatic exercise therapy
Intervention Type
Device
Intervention Name(s)
Lokomat treadmill training
Other Intervention Name(s)
Robotic Body Weight Supported Locomotor Training
Intervention Description
Lokomat treadmill training: 12 wks, 3x/wk, 45 mins@session
Intervention Type
Other
Intervention Name(s)
Aquatic exercise therapy
Other Intervention Name(s)
Aquatic Therapy
Intervention Description
Aquatic exercise training: 12 wks, 3x/wk, 45 mins@session
Primary Outcome Measure Information:
Title
Number of Participants Demonstrating 10% Change: Arm Ergometer and Lokomat Metabolic Cart VO2 Peak
Description
Peak VO2 via Arm Ergometer and Lokomat with metabolic cart
Time Frame
7 months
Secondary Outcome Measure Information:
Title
Number of Movement Recorded by Activity Monitor (SAM)
Description
SAM movements not just steps were gathered one time pre, crossover and post and worn on ankle for 5 days; percent change for each intervention
Time Frame
7 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-65 years Level of injury between C4 and T12 based on ASIA classification Chronic (greater than 12 months) spinal injury Completion of all conventional inpatient rehabilitation therapy Motor incomplete spinal cord injury (AIS C or D) Competency to provide informed consent Ability to tolerate a standing frame for at least 30 minutes Exclusion Criteria: Currently performing aquatic therapy or Lokomat training as part of clinical care Complete or concurrent lower motor neuron injury as defined by the absence of reflexes bilaterally at the knees and the ankles Uncontrolled seizures Skin opening greater than 2 cm in diameter Alcohol consumption > 3 oz liquor, or 3 x 4oz of wine, or 36 oz of beer per day Cardiac history of (a) unstable angina, (b) recent (< 3 months) myocardial infarction, (c) congestive heart failure (NYHA category II), or (d) hemodynamically significant valvular dysfunction Medical history of (a) recent hospitalization for severe disease or surgery, (b)undiagnosed diabetics (fasting glucose > 120) or poorly controlled diabetics (those not on a stable regimen for >6 months) unable to be controlled with medical treatment, (c) significant orthopedic or chronic pain conditions limiting exercise, (d) active neoplastic disease, (e) pulmonary or renal disease, and (f) presence of any serious medical condition with a prognosis for death or dependency in the next 2 months History of long bone fracture in the legs Frequent bouts of autonomic dysreflexia (as determined by the principal investigator) Any other medical co-morbidities that based on the judgment of the local principal investigator would preclude safe participation in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paula R Geigle, PT, PhD
Organizational Affiliation
University of Maryland Rehabilitation and Orthopaedic Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peter H Gorman, MD, FAAN
Organizational Affiliation
University of Maryland, Baltimore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shepherd Center, Virginia C. Crawford Research Institute
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30309-1465
Country
United States
Facility Name
University of Maryland Rehabilitation & Orthopaedic Institute (formerly known as Kernan Hospital)
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21207
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30659286
Citation
Gorman PH, Scott W, VanHiel L, Tansey KE, Sweatman WM, Geigle PR. Comparison of peak oxygen consumption response to aquatic and robotic therapy in individuals with chronic motor incomplete spinal cord injury: a randomized controlled trial. Spinal Cord. 2019 Jun;57(6):471-481. doi: 10.1038/s41393-019-0239-7. Epub 2019 Jan 18.
Results Reference
derived

Learn more about this trial

Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury

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