Restoring Walking in Non-ambulatory Children With Severe Chronic Spinal Cord Injury (SCI) (Kids STEP Study)

Sponsor
University of Florida (Other)
Overall Status
Completed
CT.gov ID
NCT00488280
Collaborator
The Craig H. Neilsen Foundation (Other), Brooks Rehabilitation (Other), Baylor College of Medicine (Other)
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Study Details

Study Description

Brief Summary

The Kids STEP Study aims to

  1. Determine if walking can be restored in children with incomplete SCI and little to no leg movement

  2. Identify the neural pathways that permit recovery of walking

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Locomotor Training
Phase 1

Detailed Description

Locomotor training (LT) is an activity-based therapy to promote plasticity and recovery of walking. It is based on animal studies investigating walking recovery after spinal cord injury and the nervous system's control of walking. Normal walking is achieved through the interaction of multiple levels of the neural axis (cortex, brain stem, spinal cord). However, a basic rhythmic walking pattern is generated by central pattern generators (CPGs) located within the spinal cord. Investigations of central pattern generators indicate that sensory input specific to the task of walking can enhance the firing of these spinal neuronal centers. Thus, LT is an intensive walking program designed to provide sensory input to the spinal cord so that the neural output from the spinal CPGs can be maximized. In addition, LT uses a treadmill and a harness to provide partial body weight support enabling persons with injury to repetitively practice walking in a safe, enabling environment.

Children enrolled in the study (after medical clearance and consent to participate) will undergo extensive testing and complete 12 weeks of locomotor training. Testing will examine the child's neurologic and functional status. Tests to examine functional status include: ASIA evaluation of sensory and motor function, gait analysis, comprehensive strength tests, and assessment of skills such as cycling, stepping, and kicking. Tests to examine the child's neurologic injury include: MRI, Transcranial Magnetic Stimulation (TMS), and reflex testing. Locomotor training will be conducted daily (5 days/ week) for a total of 60 sessions over 12 weeks. During training children will work closely with therapists, researcher, and trainers to practice walking skills on the treadmill and over-ground.

Study Design

Study Type:
Interventional
Actual Enrollment :
7 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Restoring Walking in Non-ambulatory Children With Severe Chronic SCI (Kids STEP Study)
Study Start Date :
Feb 1, 2007
Actual Primary Completion Date :
Sep 1, 2012
Actual Study Completion Date :
Sep 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Kids Step Study: Locomotor Training

All children who participate will be in the experimental cohort, KSS-#, and receive 60 sessions of daily locomotor training. This experimental cohort will also undergo clinical and neurophysiological testing pre, during, and post 60 sessions of locomotor training.

Behavioral: Locomotor Training
Task-specific practice of walking with assistance from trainers using body weight support and treadmill followed by training over ground, 5x/week, approximately 1.5 hours/day
Other Names:
  • body weight supported treadmill training
  • activity-based therapy
  • Outcome Measures

    Primary Outcome Measures

    1. Recovery of walking, assessed in treadmill/ BWS environment and overground [pre-training, after 20, 40, and 60 sessions of locomotor training]

    Secondary Outcome Measures

    1. Amount of daily step activity [during and post 60 sessions of locomotor training]

    2. Walking independence, WISCI II [during and post 60 sessions of locomotor training]

    3. Stepping assessment and kinematic analysis [Post 20, 40, and 60 sessions of locomotor training]

    4. Analysis of locomotor tasks such as crawling, swimming, cycling [post 20, 40, and 60 sessions of locomotor training]

    5. Self-selected and fast gait speed [Pre-training and after 20, 40, 60 sessions (post-LT)]

    6. Spinal MRI to assess injury [Pre-training]

    7. Spinal reflex assessment (H reflex) [Pre-training and post-training]

    8. Correlation of locomotion recovery and isolated voluntary leg movement (ASIA motor score) [Pre-training and post-training]

    9. Correlation and assessment of reticulospinal tract (Acoustic startle reflex)with recovery of locomotion [Pre-training and post-training]

    10. Correlation and assessment of corticospinal tract integrity via transcranial magnetic stimulation [Pre-training and post-training]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    3 Years to 13 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    Individuals with SCI will include:
    • Pre-adolescent children, ages 3-13 yrs old

    • A diagnosis of first time, non-progressive SCI, upper motor neuron lesion, including, but not limited to, etiology from trauma, inflammation, vascular, surgical re-section due to localized tumor removal or orthopedic pathology resulting in clinical signs of lower cervical or thoracic spinal cord injury

    • Non-ambulatory or impaired ambulation for greater than 1 yr, such that physical assistance and the use of assistive devices (i.e. walker) and/or leg braces (i.e. knee- ankle- foot orthoses (KAFOs)) are required to ambulate

    • A SCI as defined by the American Spinal Injury Association (ASIA) Impairment Scale category B or C

    • A medically stable condition that is asymptomatic for bladder infection, decubiti, osteoporosis, cardiopulmonary disease, pain, or other significant medical complications that would prohibit or interfere with testing of walking function and training or alter compliance with a training protocol

    • Documented medical approval from the participant's personal physician verifying the participant's medical status

    • Parent's informed consent for children

    Exclusion Criteria

    Children with SCI who -

    • Are currently participating in a rehabilitation program or another research protocol that could interfere or influence the outcome measures of the current study

    • Have a history of congenital SCI (e.g. Chiari malformation, myelomeningocele, intraspinal neoplasm, Frederich's ataxia) or other degenerative spinal disorders (e.g. spinocerebellar degeneration or syringomyelia) that may complicate the treatment and/or evaluation procedures

    • Children who are diabetic or have implants, pacemakers, or devices which are not NMR/MRI compatible and are not suitable for the study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Florida Gainesville Florida United States 32610

    Sponsors and Collaborators

    • University of Florida
    • The Craig H. Neilsen Foundation
    • Brooks Rehabilitation
    • Baylor College of Medicine

    Investigators

    • Principal Investigator: Andrea L Behrman, PhD, PT, University of Florida
    • Principal Investigator: Dena R Howland, PhD, OT, University of Florida

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of Florida
    ClinicalTrials.gov Identifier:
    NCT00488280
    Other Study ID Numbers:
    • 313-2006
    First Posted:
    Jun 20, 2007
    Last Update Posted:
    Jan 8, 2013
    Last Verified:
    Jan 1, 2010

    Study Results

    No Results Posted as of Jan 8, 2013