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Retraining Walking after Spinal Cord Injury - Article


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Patau syndrome

Bartholin-Patau syndrome; Chromosomal imbalance syndrome, pair 13, trisomy; chromosome 13 trisomy syndrome; D1 Trisomy; Trisomy 13 syndrome


Clinical Trial: Retraining Walking after Spinal Cord Injury

This study is currently recruiting patients.

Sponsors and Collaborators: National Institute of Child Health and Human Development (NICHD)
Department of Veterans Affairs
Information provided by: National Institute of Child Health and Human Development (NICHD)

Purpose

Incomplete spinal cord injury often results in difficulty walking. Training on a treadmill with body weight support may improve walking ability after spinal cord injury. The purpose of this study is to examine the effect of treadmill speed on spinal cord function and walking performance.

Condition Treatment or Intervention Phase
Spinal Cord Injuries
Quadriplegia
Paraplegia
Central Cord Syndrome
Brown-Sequard Syndrome
 Behavior: Locomotor treadmill training with body weight support
Phase II
Phase III

MedlinePlus related topics:  Paralysis;   Spinal Cord Injuries

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study

Official Title: Activity-dependent Plasticity after Spinal Cord Injury

Further Study Details: 

Expected Total Enrollment:  16

Study start: May 2000;  Expected completion: January 2005

Conventional rehabilitation following spinal cord injury (SCI) emphasizes functional gains through strengthening and compensation, using braces and assistive devices to achieve mobility. Rehabilitation practice using compensatory approaches is based on the prevailing assumption that neural recovery is not possible following SCI.

Recent evidence contradicts this assumption. Stimulated by the proper activation of peripheral afferents associated with walking, neuronal circuits may reorganize by strengthening of existing and previously inactive descending connections and local neural circuits. New approaches to locomotor recovery after SCI utilize sensory information related to locomotion to improve treadmill and overground walking.

Locomotor training velocity may be a critical, task-specific, and activity-dependent parameter affording appropriate phasic, afferent input to the neural system and promoting neural plasticity. The purpose of this study is to evaluate the effects of training velocity in a long-term locomotor training program on both neurophysiological and behavioral plasticity in individuals with incomplete SCI.

Sixteen patients with incomplete SCI will be recruited to participate in this study. Baseline evaluations will include American Spinal Injury Association classification, rate-sensitive depression, phase-dependent H-reflex modulation at self-selected and fast overground walking velocities, and MRI of the spine. Patients will wear a step activity monitor for a 48-hour period, quantifying baseline walking activity level.

All patients will participate in a locomotor training program. Patients will be randomly assigned to either training at self-selected treadmill velocity or at a normal walking velocity. Patients will have 45 training sessions over 9 weeks. Each training session will include 30 minutes of walking. Interim testing of rated depression, spatial-temporal parameters of walking, MRI, and walking activity will occur through the 9-week training period. Post-testing will occur within 2 days of the last training session and at a 1 month after completion of the training. During the month following long-term training, patients will be instructed to return to their self-selected routine activities of daily living.

Eligibility

Ages Eligible for Study:  6 Years   -   65 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion criteria:

  • First time spinal cord injury (SCI) from trauma, vascular, or orthopedic pathology at cervical or thoracic levels
  • Category C or D SCI as defined by the American Spinal Injury Association (ASIA) Impairment Scale
  • 1 to 3 years post-SCI
  • Ability to walk independently a minimum of 40 feet with or without an assistive device
  • Currently spending a minimum of 30 minutes per day walking
  • No change in anti-spasticity medication during the study
  • Medically stable
  • Participant’s personal physician must verify the participant’s medical status

Exclusion criteria:

  • Bladder infection, decubiti, osteoporosis, cardiopulmonary disease, pain, or other significant medical complications that would prohibit or interfere with training and testing of walking function or alter compliance with a training protocol
  • Currently participating in a rehabilitation program or another research protocol that could interfere or influence the outcome measures of the current study
  • Congenital SCI (e.g., Chiari malformation, myelomeningocele, intraspinal neoplasm, Frederich’s ataxia)
  • Other degenerative spinal disorders (e.g., spinocerebellar degeneration, syringomyelia) that may complicate the treatment or evaluation procedures

Location and Contact Information

Andrea L Behrman, PhD      352-273-6117    abehrman@hp.ufl.edu
Michelle L Woodbury, OTR, MA       mwoodbur@hp.ufl.edu

Florida
      University of Florida, Gainesville,  Florida,  32610,  United States; Recruiting
Andrea L Behrman, PhD  352-273-6117    abehrman@hp.ufl.edu 
Floyd Thompson, PhD  352-294-0033    thompson@mbi.ufl.edu 
Andrea L Behrman, PhD, PT,  Principal Investigator
Floyd J Thompson, PhD,  Sub-Investigator
Krista Vandenborne, PhD, PT,  Sub-Investigator

Study chairs or principal investigators

Andrea L Behrman, PhD,  Principal Investigator,  University of Florida   

More Information

Departmental Website for Principal Investigator

Website for Principal Investigator in Rehabilitation Science PhD Program

Publications

Behrman AL, Harkema SJ. Locomotor training after human spinal cord injury: a series of case studies. Phys Ther. 2000 Jul;80(7):688-700. Review.

Barbeau H, Norman K, Fung J, Visintin M, Ladouceur M. Does neurorehabilitation play a role in the recovery of walking in neurological populations? Ann N Y Acad Sci. 1998 Nov 16;860:377-92. Review.

Study ID Numbers:  K01HD01348
Record last reviewed:  May 2004
Last Updated:  October 14, 2004
Record first received:  April 28, 2003
ClinicalTrials.gov Identifier:  NCT00059553
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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October 7, 2008



Page Updated: September 6, 2005
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