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

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Spinal Cord Injuries

Treatments

Device: Locomotor training using a robotic device

Study type

Interventional

Funder types

Other

Identifiers

NCT01147185
EMSCI-DR

Details and patient eligibility

About

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.

Full 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.

Enrollment

21 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

21 participants in 2 patient groups

Intensive training
Other group
Description:
Locomotor training using a robotic device of at least 50 minutes
Treatment:
Device: Locomotor training using a robotic device
Device: Locomotor training using a robotic device
Standard training
Active Comparator group
Description:
Locomotor training using a robotic device of maximally 25 minutes
Treatment:
Device: Locomotor training using a robotic device
Device: Locomotor training using a robotic device

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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