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Completed

NCT Number: NCT01147185

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Berufsgenossenschaftliche Unfallklinik Murnau, Murnau am Staffelsee, Germany

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Locomotor training using a robotic device

Device

50min walking time, 3-5 trainings/week.

Other names: Lokomat, Hocoma AG, Volketswil/Switzerland

Primary outcomes

  1. 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

  1. Walking Index for Spinal Cord Injury (WISCI)

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

    Classification of walking ability on a rank ordered scale with 21 categories.

  2. Spasticity

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

    Muscle tone is rated using the modified Ashworth and the Pess spasm frequency tests

  3. Perceived exertion

    Time frame: after every training

  4. Spinal Cord Independence Measure

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

  5. Spinal cord injury classification

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

    Classification according to the standards by the American Spinal Cord Injury Association (ASIA)

  6. Patients' Global Impression of Change Scale

    Time frame: At week 8

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Registry information

Important dates

Study start
2010
Primary completion
2016
Study completion
2016
First posted
Jun 22, 2010
Registry last updated
Jun 29, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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