Brain wave test may finally distinguish real tics from functional ones
NCT ID NCT07137442
First seen Jun 27, 2026 · Last updated Sep 18, 2026 · Updated 58 times
Summary
This study aims to find differences between organic tics (related to diagnosed disorders) and functional tics (caused by problems in brain-body communication). Researchers will use sensors to measure muscle activity and brain waves in 75 adults with tics and healthy volunteers. Participants undergo a single 4-hour session of monitoring and questionnaires. The goal is to improve diagnosis, not to test a treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better diagnostic tools to tell apart organic tics from functional tics.
- What could go wrong
- This is an early observational study with only 75 participants. It does not test a treatment, so results may not change clinical practice directly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 75 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2034
An estimate. End dates often move.
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Three groups with up to 25 subjects in each group. Two groups of patients (18-80 years old) with tics and functional tics, and another group of healthy controls.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* INCLUSION CRITERIA: In order to be eligible to participate in this study, an individual must meet all of the following criteria: * Capacity to provide informed consent (self-consent) * Stated willingness to comply with all study procedures and availability for the duration of the study * Male or female, aged 18-80 * Agreement to adhere to Lifestyle Considerations prior to and during the physiological testing visit. Inclusion criteria for patients with functional tics or tics \- Diagnosed with functional motor tics or motor tics Inclusion criteria for healthy controls \- Have no neurological or psychiatric disorders established by history and physical/neurological examination EXCLUSION CRITERIA: * Self-reported consumption of \>14 alcoholic drinks/week\* for a man and \>7 alcoholic drinks/week for a woman * Use of prescription drugs and other illicit drugs that may suppress tics such as dopamine blocking agents and antipsychotics during a certain time period prior to the neurophysiological testing session.\*\* * Clinically significant abnormal movements on neurological examination except for tics. * Contraindications to EEG or EMG procedures, including skin lesions at electrode sites or hypersensitivity to electrode materials. * History of or current brain tumor, stroke, head trauma with loss of consciousness. * Epilepsy or seizures in the past 12 months. * Have a Baclofen pump, or have neurostimulators for pain. * Pregnant women * Self-reported current major depression or Beck Depression Inventory II (BDI-II) score \>19, Generalized Anxiety Disorder 7-item scale (GAD-7) score \> 9, or any major current psychiatric illness. * Presence of any metal in the eye or skull area such as a brain stimulator, shrapnel, surgical metal, clips in the brain, cochlear implants, metal fragments in the eye. * Presence of pacemaker, intracardiac lines, implanted pumps or stimulators. * Unable to comply with the requirements of the study procedures. * Vocal tics only tested with Modified Rush Video-Based Tic Rating Scale. * Low Premonitory Urge for Tics Scale (PUTS) score \< 9 (maximum 36) with low willingness for tics (patient groups only, not applicable in healthy volunteers). * Note: 1 standard alcoholic drink is 0.6 ounce (14 grams) of pure alcohol. * Note: The certain time period depends on different drugs used. Five half-lives will be selected. The drug is considered effectively eliminated from the body after this time period because the concentration of the drug reaches around 3% of the orininal concentration.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
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