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Clinical Trials/NCT01147185
NCT01147185CompletedNot Applicable

Effectiveness of Automated Locomotor Training in Patients With Acute Incomplete Spinal Cord Injury: A Multicenter Trial

University of Zurich4 sites in 3 countries21 target enrollmentStarted: February 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
21
Locations
4
Primary Endpoint
Ten meter walking test

Study Overview

Brief Summary

The purpose of this study is to determine whether longer locomotor training results in a mor favorable outcome in patients with incomplete spinal cord injury.

Detailed Description

About half of patients who experience a traumatic spinal cord injury (SCI) have still motor and/or sensory function below the level of the lesion. A large proportion of these patients become ambulatory within the first six months after the SCI. In order to optimally train the walking function patients are partially unloaded from their body weight while they walk on a moving treadmill. In severe cases therapists have to assist the leg movements which is an exhaustive work limiting training time. In the last few years robotic devices have been developed which enable longer training time. Studies evaluating the training of patients with hemiparesis showed that longer training time is associated with a better outcome. The present study aims at evaluating the effect of training time within the robotic device on the recovery of ambulatory function. Subject with an acute incomplete SCI will be included. The intervention consist of a walking training which lasts at least 50min, the training of the control group last at maximum 25min. Both groups will undergo 3-5 trainings per week. Group assignment will be performed at random. The study lasts for 8 weeks. The primary outcome will be the self selected walking speed which will be assessed bi-weekly during the training period and 4 months later.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •patients with spinal cord injury (SCI) categorized according to the standard classification of the American Spinal Injury Association as ASIA B or C within the first two weeks after trauma
  • •traumatic etiology of SCI
  • •limited walking ability (Walking Index for Spinal Cord Injury ≤5)
  • •able to start training or rehab within 60 days after trauma
  • •motor level between cervical 4 and thoracic 12
  • •signed informed consent

Exclusion Criteria

  • •exclusion criteria of the Lokomat:(bodyweight > 130kg, body height > 200cm, leg length diff > 2cm, osteoporosis, instable fracture of lower extremity, restricted range of motion, decubitus ulcer of lower extremity)
  • •concomitant injury limiting walking ability (e.g. lower extremity fractures, instable spine fractures, Joint instability preventing weight-bearing, severe soft tissue lesion)
  • •pre-existing medical conditions interfering with unrestricted walking (e.g. total joint replacement, pain, osteoarthritis, polyneuropathy, cardiopulmonary disease)
  • •age older than 65 years or younger than 18 years
  • •conus medullaris or cauda equina syndrome
  • •traumatic brain injury
  • •passive range of motion of the hips, knees and ankles not sufficient to allow normal kinematics consistent with upright gait
  • •patient participates in other rehabilitation or pharmacological study

Arms & Interventions

Intensive training

Other

Locomotor training using a robotic device of at least 50 minutes

Intervention: Locomotor training using a robotic device (Device)

Standard training

Active Comparator

Locomotor training using a robotic device of maximally 25 minutes

Intervention: Locomotor training using a robotic device (Device)

Outcomes

Primary Outcomes

Ten meter walking test

Time Frame: at start of training, at weeks 2, 4, 6, 8, 6 and 24

Self selected walking speed over a distance of 10m

Secondary Outcomes

  • Patients' Global Impression of Change Scale(At week 8)
  • Perceived exertion(after every training)
  • Spinal Cord Independence Measure(at start of training, at weeks 2, 4, 6, 8, 6 and 24)
  • Walking Index for Spinal Cord Injury (WISCI)(at start of training, at weeks 2, 4, 6, 8, 6 and 24)
  • Spasticity(at start of training, at weeks 2, 4, 6, 8, 6 and 24)
  • Spinal cord injury classification(at start of training, at weeks 2, 4, 6, 8, 6 and 24)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (4)

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