Status:

COMPLETED

In-home Telerehabilitation for Quadriplegic Hand Function

Lead Sponsor:

University of Alberta

Collaborating Sponsors:

International Spinal Research Trust

Alberta Heritage Foundation for Medical Research

Conditions:

Spinal Cord Injury

Quadriplegia

Eligibility:

All Genders

18+ years

Phase:

PHASE2

PHASE3

Brief Summary

1. To evaluate improvements in hand function in stable, cervical spinal cord injured (SCI) subjects treated with functional electrical stimulation (FES)-assisted exercise; 2. To compare the informatio...

Detailed Description

Chronic C5, 6 or 7 SCI subjects who have sustained a cervical SCI resulting in complete or incomplete quadriplegia. Time since injury at least one year at time of entry to study. Subjects may have a c...

Eligibility Criteria

Inclusion

  • Chronic C5, 6 or 7 SCI subjects who have sustained a cervical SCI resulting in complete or incomplete quadriplegia. Time since injury at least one year at time of entry to study. Subjects may have a complete or an incomplete injury but must demonstrate loss of finger grasp and release as well as loss of thumb lateral (key) pinch bilaterally or unilaterally. Subjects must be stable neurologically and medically, cognitively intact, and willing and able to attend the requisite appointments for participation in the study.

Exclusion

  • Subjects with unresolved medical issues such as easily triggered autonomic dysreflexia and/or hypotension.
  • Subjects demonstrating severe spasticity affecting the upper extremities, fixed hand contractures with loss of suppleness and range of movement at the metacarpal-phalangeal joints, absence of voluntary ability to extend the wrist against gravity and/or insufficient muscle strength to abduct (lift) the arm against gravity.
  • Subjects with unresolved substance abuse problems
  • Subjects with a history of head injury, epilepsy in self or close relative and/or cognitive impairment
  • Subjects with intracranial metal inclusions
  • Subjects, who upon initial testing, demonstrate partial or complete denervation (loss of nerve supply) of the nerves to the the targeted muscle.

Key Trial Info

Start Date :

May 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2010

Estimated Enrollment :

13 Patients enrolled

Trial Details

Trial ID

NCT00656149

Start Date

May 1 2007

End Date

December 1 2010

Last Update

January 12 2017

Active Locations (1)

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1

Centre for Neuroscience, University of Alberta

Edmonton, Alberta, Canada, T6C1M8