Transcranial Magnetic Stimulation and Electrical Stimulation of Nerves to Study Focal Dystonia



Status:Completed
Conditions:Neurology, Orthopedic
Therapuetic Areas:Neurology, Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:November 2002
End Date:September 2008

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The Effect of Peripheral Heterotopic Stimulation on Cortical Excitability in Dystonia

This study will use transcranial magnetic stimulation (TMS) and electrical stimulation of
nerves to examine how the brain controls muscle movement in focal hand dystonia (writer's
cramp). Normally, when a person moves a finger, the brain's motor cortex prevents the other
fingers from moving involuntarily. Patients with focal hand dystonia have difficulty with
individualized finger movements, possibly due to increased excitability of the motor cortex.
Musicians, writers, typists, athletes and others whose work involves frequent repetitive
movements may develop focal dystonia of the hand.

Healthy normal volunteers and patients with focal dystonia 18 years of age and older may be
eligible for this study.

For the TMS procedure, subjects are seated in a comfortable chair with their hands placed on
a pillow on their lap. An insulated wire coil is placed on the scalp. A brief electrical
current is passed through the coil, creating a magnetic pulse that stimulates the brain.
This may cause muscle, hand or arm twitching if the coil is near the part of the brain that
controls movement, or it may induce twitches or transient tingling in the forearm, head or
face muscles. Subjects will be asked to move a finger. Just before this movement, a brief
electrical stimulation will be applied to the end of either the second or fifth finger.
Metal electrodes will be taped to the skin over the muscle for computer recording of the
electrical activity of the hand and arm muscles activated by the stimulation. The testing
will last 2-3 hours.

The purpose of this study is to investigate the effect of sensory afferent input on surround
inhibition in the motor cortex in dystonia. Surround inhibition is a cortical phenomenon,
the function of which may be to suppress unwanted movements in surrounding muscles during
voluntary actions. In support of this, a recent study showed that motor output to the little
finger was reduced during self-paced, voluntary movements of the index finger, despite an
increase in spinal excitability. Work has also shown that in relaxed muscles, homotopic and
heterotopic peripheral stimulation results in time dependent modulation of motor cortical
excitability. However, no studies have examined the relationship between volitional movement
and sensory input on cortical surround inhibition, the phenomenon which we hypothesize to be
defective in dystonia. The aim of this study then is to examine the changes in surround
inhibition when electrical stimulation is applied to the finger being actively moved,
leading to an inhibition of a surrounding finger (heterotopic inhibition), at different time
intervals prior to the initiation of movement, to assess the effect of heterotopic
peripheral stimulation on surround inhibition in dystonia patients compared to normal
subjects.

- INCLUSION CRITERIA:

Nineteen patients age 18 and over with focal dystonia of the upper limbs (writer's cramp)
will be recruited for the study.

For patients, the only selection criteria are the presence of focal hand dystonia.

Nineteen normal subjects age 18 and over will be recruited for the control group.

The controls will not have dystonia or any other neurological condition.

All subjects will sign an informed consent prior to participation in the trial.

EXCLUSION CRITERIA:

Exclusion criteria for the trial covering both the normal control and dystonia group will
include any concurrent medical or surgical condition as well as neurological or
psychiatric illnesses.

Exclusion criteria will include any individual who is on medications with potential
influence of the nervous system function (antidepressants, anxiolytics, anticonvulsants,
antipsychotic, antiparkinson, hypnotics, stimulants, and antihistamines).

The exclusion criteria also include patients who have received Botulinum toxin injection
within 3 months of starting the protocol.

Furthermore, any individual who has a pacemaker, an implanted medical pump, a metal plate
or metal object in the skull or eye (for example, after brain surgery), or who has a
history of seizure disorder will be excluded from the trial.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
?
mi
from
Bethesda, MD
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