Neural Control of Bilateral Movements After SCI



Status:Recruiting
Conditions:Hospital, Orthopedic
Therapuetic Areas:Orthopedics / Podiatry, Other
Healthy:No
Age Range:18 - 85
Updated:3/7/2019
Start Date:March 2015
End Date:December 2019
Contact:Monica A Perez, PhD, PT
Email:mperez04@sralab.org
Phone:305-243-7119

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Neural Control of Bilateral Hand, Arm, and Leg Movements After Spinal Cord Injury

The long‐term goal is to acquire scientific knowledge that can be used to develop
mechanistic-driven intervention strategies aiming at restoring upper and lower-limb motor
function in individuals with cervical or thoracic spinal cord injury (SCI). The proposed
project will examine cortical, corticospinal, and spinal contribution to bilateral hand and
arm muscle activity during bilateral movements and spinal contributions to lower limb muscle
activity. By comparing changes in different sites within the Central Nervous System (CNS),
the investigators may also identify key mechanisms that might be differentially affected by
the injury, plasticity, and training.

If the participant qualifies to take part in this research study, they will be asked to
participate in 15-190 study visits,to complete the experimental procedures. These procedures
have been broken up into "Phases" and will be completed in any order. Phase I and Phase IIa
includes 2-30 total visits - approximately 2-3 hours each to measure arm and finger strength
and ability to move. Phase IIb includes 2-30 total visits - approximately 2-3 hours each, to
measure leg strength and ability to move. Phase IIIa includes up to 40 total visits -
approximately 2 hours each, the investigator will again evaluate the participant's ability to
use both arms. The participant will be asked to complete a series of tasks such as stacking
checkers, turning over cards, squeeze a device to determine how strong their grip is, and see
how well they are able to feel sensations on the surface of their skin. The investigators
will complete these assessments at pre-determined times during the study participation. Phase
IIIb includes up to 40 total visits - approximately 2 hours each, the investigator will again
evaluate the participant's ability to use both legs. Assessments of the participant's legs
will include walking around the lab space, how well they can bend their ankles and hips, and
how well they are able to feel sensations on the surface of the participant's skin.

Inclusion Criteria:

- Inclusion criteria for individuals with SCI:

- Male and females between ages 18-85 years

- SCI (≥1 month after injury)

- Cervical, thoracic or lumbar injury above L5 (tetraplegia)Intact (level 2) or
impaired (level 1) but not absent (level 0) lower motor neuron innervations in
dermatomes C6, C7 and C8 during light touch and pin prick stimulus using the
American Spinal Injury Association (ASIA) sensory scores (12)

- The ability to produce a visible precision grip force with both hands

- Individuals who have the ability to pick up a small object (large paperclip) from
a table independently

- Ability to perform 30° or more of elbow flexion and extension.

- The ability to perform a visible contraction with dorsiflexor and hip flexor
muscles

- The ability to ambulate a few steps with or without an assistive device

Inclusion criteria for healthy controls:

- Male and females between ages 18-85 years

- Right handed

- Able to complete precision grips with both hands

- Able to complete full elbow flexion-extension with both arms.

- Able to walk and complete lower-limb tests with both legs.

Exclusion Criteria:

- Exclusion criteria for individuals with SCI and Healthy Controls:

- Uncontrolled medical problems including pulmonary, cardiovascular or orthopedic
disease

- Any debilitating disease prior to the SCI that caused exercise intolerance

- Premorbid, ongoing major depression or psychosis, altered cognitive status

- History of head injury or stroke

- Pacemaker

- Metal plate in skull

- History of seizures

- Receiving drugs acting primarily on the central nervous system, which lower the
seizure threshold such as antipsychotic drugs (chlorpromazine, clozapine) or
tricyclic antidepressants

- Pregnant females

- Ongoing cord compression or a syrinx in the spinal cord or who suffer from a
spinal cord disease such as spinal stenosis, spina bifida or herniated cervical
disk.
We found this trial at
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Miami, Florida 33136
Phone: 305-243-7119
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