Role of the Sensory Experience in Generating Motor Tics in Tourette Syndrome

Completed

Conditions studied: Tic Disorder, Tourette Syndrome

In brief

This study will investigate the sensation that many people with Tourette syndrome (TS) experience before they have a motor tic. It will also test whether blocking the sensation causes the tic to stop. People between 18 and 65 years of age with TS who have at least once tic involving an arm may be eligible for this 3-part study. Those enrolled may participate in all parts or in part 1 or part 2. Those who choose to participate in part 3 must first complete part 2. All must stop taking medication for TS and any other medication that may affect the brain for at least 1 week before the study. Part 1 After numbing the skin or muscles of the arm or leg where a pre-tic sensation is experienced, the response of the nerves will be tested by asking subjects to rate the strength of the sensation after a pinprick and by stimulating the nerves with small electrical shocks. Then, over the course of approximately one hour, subjects will report pre-tic sensations while their motor tics are counted. The onset of each tic will be identified with EMG, a test using electrodes on the skin to indicate the activity of the muscles. Part 2 Subjects brain waves are recorded using magnetoencephalography (MEG) while they are experiencing tics andpre-tic sensory experiences. MEG is a test that records magnetic field changes produced by brain activity. Subjects sit in a chair under a dome containing magnetic field detectors. They watch a clock and report the time a sensory experience starts. Tics are recorded with EMG. Later, a standard MRI of the brain (scan using a magnetic field and radio waves) is done to see which parts of the brain produced the activity recorded with MEG. Part 3 Repetitive transcranial magnetic stimulation (rTMS) is used to try to stop the pre-tic sensations. For TMS, the subject sits in a chair. A wire coil is held on the subject s scalp, and a brief electrical current is passed through the coil, creating a magnetic pulse that stimulates a region of the brain. The goal of this stimulation is to reduce the sensory experience that precedes a tic in one region of the body. During stimulation, the subject hears a click and may feel a pulling sensation on the skin under the coil. There may be a twitch in the muscles of the face, arm or leg. This study uses a pattern of repeated pulses delivered in short bursts. Following each train of pulses, the effect of the stimulation on sensation will be tested by asking the subject to rate the strength of a pinprick and of a vibration. In addition, the nerves are stimulated with small shocks to evaluate the effect of the TMS on nerve activity. To determine the effect of TMS on the pre-tic sensation, subjects are asked to watch a clock and report when they are having a sensory experience. The effect on motor tics will be evaluated by using EMG to indicate the tics.

Key facts

Study ID

NCT00755339

Run by

National Institute of Neurological Disorders and Stroke (NINDS)

People needed

54

Starts

2008-09-15

Expected to finish

2016-10-25

Last updated by the study team

2019-10-25

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may not qualify if…

• Inability to stop taking all central-acting medications, including those used to treat tics, for at least one week prior to the study
• Current use of coumadin, heparin, or lovenox
• Any additional movement disorder, including tremor, myoclonus, or dystonia
• A diagnosis of major depression or bipolar disorder
• Frequent or severe headaches
• Any history of or current experience of hallucinations
• Any history of a seizure or epilepsy or a family history of epilespy
• Any prior brain injury, brain tumor or other lesion, stroke, or surgery
• A diagnosis of increased intracranial pressure
• A history of significant heart disease
• Any history of hearing problems, or abnormal results on auditory testing (part I or II)
• Any of the following: pacemakers or other implanted electrical devices, brain stimulators, dental implants, aneurysm clips (metal clips on the wall of a large artery), metallic prostheses (including metal pins and rods, heart valves, and cochlear implants), permanent eyeliner, implanted delivery pump, or shrapnel fragments (part I and II only)
• Any history of work as a welder or metal worker (part I and II)
• Current pregnancy
• Tobacco use (cigarette, chewing, or other) in the month prior to the study (part II)
• Diagnosis of, treatment for, or self-report of alcohol abuse (alcoholism) (part I)
• Cocaine use in the year prior to involvement in the study (part I)
• Use of any medication within one month prior to the study with cholinergic or anticholinergic properties, including (but not limited to): nicotine patch, nicorette gum, atrovent, enablex, toriaz, ditropan, vesicare, detrol, sanctura, artane, Aricept, cogentin, akineton, zanaflex, norflex, flexeril, lomotil, mototen, levsin, razadyne, exelon (part I)
• Peripheral neuropathy or carpal tunnel syndrome (part I)
• Inability to hold head still for 10 minutes (part I).

Where it is running

• National Institutes of Health Clinical Center, 9000 Rockville Pike — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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