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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03592173
Other study ID # BRC391
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date July 2013
Est. completion date December 2019

Study information

Verified date July 2019
Source Burke Medical Research Institute
Contact Mar Cortes, MD
Phone 9143683181
Email mac2083@med.cornell.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if spinal excitability is increased with a Spinal Associative Stimulation (SAS) protocol, and to determine the functional consequences of this technique on motor recovery.


Description:

Recovery of motor function continues to be a problem following Spinal Cord Injury. Non-invasive brain stimulation techniques, targeting cortical areas, have been shown to enhance the excitability in the human motor cortex, and these changes in the motor cortex may be of significance for the rehabilitation of brain injured patients. However, little is known about the adaptational changes in the excitability/plasticity of spinal neural circuits in spinal cord injury patients.

The purpose of this study is to investigate the excitability of cortical and spinal inhibitory and excitatory mechanisms before and following a period of repetitive and synchronized dual peripheral nerve and brain stimulation. Repetitive, paired brain and peripheral nerve stimulation as a neuromodulatory tool, paired associative stimulation (PAS), has been well described. In this technique, stimuli are timed such that afferent and efferent volleys interact at the level of the cortex, that lead to a temporary enhancement of Motor Evoked Potential (MEP) amplitude in target muscles, and when applied repeatedly, lead to a sustained effect, outlasting the intervention period. This repetitive technique has been done in healthy subjects and patients with neurological diseases. By modifying the time between paired stimuli, the investigators will generate afferent/efferent interactions in the spinal cord.

The working hypothesis of this study is that the acute facilitation of the H-reflex during Paired TMS and peripheral nerve stimulation, may be harnessed to modulate spinal excitability (sustained increase in the MEP amplitude). That is, the investigators will test if similar to PAS, a change in excitability outlasting the stimulation/intervention period may occur with afferent/efferent interactions, although at the level of the spinal cord rather than the cortex, and be useful to strengthen residual pathways after damage to the spinal cord.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 2019
Est. primary completion date September 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Spinal cord injury subjects with chronic lesions (> 6 months after the injury)

- Motor incomplete lesion, measured by the American Spinal cord Injury Association (ASIA) Impairment Scale (AIS)

- Traumatic cause of lesion; d) Some degree of motor function in the ankle flexor and extensors (Low extremity Motor Score - LEMS=3).

Exclusion Criteria:

- Motor and sensory complete lesion (AIS A); LEMS < 3;

- Non-traumatic cause of lesion

- Medically unstable condition

- Other concurrent neurological illness

- Presence of a potential TMS risk factor (detailed below)

Potential TMS risk factor:

- Damaged skin at the site of stimulation

- Presence of an electrically, magnetically or mechanically activated implant

- An intracerebral vascular clip, or any other electrically sensitive support system

- Metal in any part of the body, including metal injury to the eye

- A history of medication-resistant epilepsy in the family

- Past history of seizures or unexplained spells of loss of consciousness.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Paired TMS & Peripheral Nerve Stimulation
Method of assessing neurophysiology and activity of the spinal cord

Locations

Country Name City State
United States Burke Medical Research Institute White Plains New York

Sponsors (2)

Lead Sponsor Collaborator
Kathleen Friel Burke Medical Research Institute

Country where clinical trial is conducted

United States, 

References & Publications (14)

Boorman G, Becker WJ, Morrice BL, Lee RG. Modulation of the soleus H-reflex during pedalling in normal humans and in patients with spinal spasticity. J Neurol Neurosurg Psychiatry. 1992 Dec;55(12):1150-6. — View Citation

Deletis V, Schild JH, Beric A, Dimitrijevic MR. Facilitation of motor evoked potentials by somatosensory afferent stimulation. Electroencephalogr Clin Neurophysiol. 1992 Oct;85(5):302-10. — View Citation

Hiersemenzel LP, Curt A, Dietz V. From spinal shock to spasticity: neuronal adaptations to a spinal cord injury. Neurology. 2000 Apr 25;54(8):1574-82. — View Citation

Höffken O, Veit M, Knossalla F, Lissek S, Bliem B, Ragert P, Dinse HR, Tegenthoff M. Sustained increase of somatosensory cortex excitability by tactile coactivation studied by paired median nerve stimulation in humans correlates with perceptual gain. J Physiol. 2007 Oct 15;584(Pt 2):463-71. Epub 2007 Aug 16. — View Citation

Kofler M, Valls-Solé J, Fuhr P, Schindler C, Zaccaria BR, Saltuari L. Sensory modulation of voluntary and TMS-induced activation in hand muscles. Exp Brain Res. 2008 Jul;188(3):399-409. doi: 10.1007/s00221-008-1372-2. Epub 2008 Apr 18. — View Citation

Kumru H, Vidal J, Kofler M, Benito J, Garcia A, Valls-Solé J. Exaggerated auditory startle responses in patients with spinal cord injury. J Neurol. 2008 May;255(5):703-9. doi: 10.1007/s00415-008-0780-3. Epub 2008 Feb 21. — View Citation

Pascual-Leone A, Tarazona F, Keenan J, Tormos JM, Hamilton R, Catala MD. Transcranial magnetic stimulation and neuroplasticity. Neuropsychologia. 1999 Feb;37(2):207-17. — View Citation

Pascual-Leone A. Disrupting the brain to guide plasticity and improve behavior. Prog Brain Res. 2006;157:315-329. Review. — View Citation

Poon DE, Roy FD, Gorassini MA, Stein RB. Interaction of paired cortical and peripheral nerve stimulation on human motor neurons. Exp Brain Res. 2008 Jun;188(1):13-21. doi: 10.1007/s00221-008-1334-8. Epub 2008 Mar 11. — View Citation

Ridding MC, McKay DR, Thompson PD, Miles TS. Changes in corticomotor representations induced by prolonged peripheral nerve stimulation in humans. Clin Neurophysiol. 2001 Aug;112(8):1461-9. — View Citation

Rothwell JC. Techniques and mechanisms of action of transcranial stimulation of the human motor cortex. J Neurosci Methods. 1997 Jun 27;74(2):113-22. Review. — View Citation

Serranová T, Valls-Solé J, Muñoz E, Genís D, Jech R, Seeman P. Abnormal corticospinal tract modulation of the soleus H reflex in patients with pure spastic paraparesis. Neurosci Lett. 2008 May 23;437(1):15-9. doi: 10.1016/j.neulet.2008.03.068. Epub 2008 Mar 28. — View Citation

Stefan K, Kunesch E, Benecke R, Cohen LG, Classen J. Mechanisms of enhancement of human motor cortex excitability induced by interventional paired associative stimulation. J Physiol. 2002 Sep 1;543(Pt 2):699-708. — View Citation

Valls-Solé J, Alvarez R, Tolosa ES. Responses of the soleus muscle to transcranial magnetic stimulation. Electroencephalogr Clin Neurophysiol. 1994 Dec;93(6):421-7. — View Citation

* Note: There are 14 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Change in H-Reflex Threshold Assessment of muscle reaction after stimulation of sensory fibers Baseline compared with immediately after intervention
Secondary Lower Extremity Motor Score (LEMS) Assessment of lower extremity strength in key muscles; maximal score of 50 with 20 or less indicating participant likely has limited ambulation. Baseline, immediately after intervention
Secondary Walking Index for Spinal Cord Injury (WISCI II) This is a functional capacity scale that rank orders ambulation in people with spinal cord injury, by evaluating the amount of physical assistance, braces or devices required to walk 10 meters. Rank scores range from 0-20. A higher score is indicative of more independent ambulation. Baseline, immediately after intervention
Secondary 10 Meter Walk Test Measure of gait speed Baseline, immediately after intervention
Secondary Spinal Cord Independence Measure, Version 3 (SCIM III) A disability rating scale developed to specifically address the ability of SCI patients to perform basic activities of daily living independently (including self-care, mobility, respiration and sphincter management) Baseline, immediately after intervention
Secondary Muscle Force Amount of force recorded during maximal voluntary isometric contraction of a grip movement, recorded with a grip strength measurement device. Baseline, immediately after intervention
Secondary Anklebot Lower extremity robotic device that provides kinematic evaluation data Baseline, immediately after intervention
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