A clap of thunder: could a hand clap diagnose seizures?
NCT ID NCT07742709
First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time
Summary
This trial tests whether a sudden, loud hand clap can help doctors quickly tell apart epileptic seizures from psychogenic non-epileptic seizures (PNES), which look similar but have different causes. About 400 people undergoing video-EEG monitoring will receive the clap test during a seizure episode, and their reactions will be recorded. The goal is to see if this simple, low-cost test can provide a fast and accurate diagnosis, potentially reducing the need for more complex procedures.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Abrupt Clap Provocation Test (a diagnostic procedure using a sudden loud hand-clap to observe reactions during seizures)
- What this could lead to
- If effective, this could provide a rapid, low-cost way to distinguish epileptic seizures from psychogenic non-epileptic seizures, improving diagnosis and treatment.
- What could go wrong
- The test's accuracy may vary, and it might not replace standard video-EEG monitoring. It's a single-center study, and results need confirmation in broader settings.
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 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of patients with suspected epilepsy referred for 24-hour continuous video-electroencephalography (VEEG) monitoring at the Department of Neurology, Xijing Hospital. Eligible participants are individuals of any gender, typically young to middle-aged adults, who experience at least one clinical paroxysmal episode with prominent convulsive or motor abnormalities during the monitoring period. The core analyzed cohort comprises patients who successfully undergo the Abrupt Clap Provocation Test (ACPT) during the ictal phase and subsequently receive a definitive diagnosis of either epileptic seizures (ES) or psychogenic non-epileptic seizures (PNES; Level 4 certainty according to the International League Against Epilepsy criteria). Patients with pre-existing severe hearing loss, other non-epileptic paroxysmal disorders (e.g., syncope, sleep disorders), or those whose seizure events are obscured or occur outside the camera's view are excluded.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Continuous video-electroencephalogram (VEEG) monitoring duration of 24 hours or longer * At least one recorded episode during VEEG monitoring with prominent abnormal limb movements (such as convulsive episodes) * Successful administration of the standardized Abrupt Clap Provocation Test (ACPT) during the clinical ictal phase * Episodes definitively diagnosed as epileptic seizures (ES) or confirmed as psychogenic non-epileptic seizures (PNES) at the highest certainty level (Level 4: documented/confirmed) according to the International League Against Epilepsy (ILAE) criteria * Complete clinical and demographic data available Exclusion Criteria: * Coexisting severe hearing impairment or documented ear disease, rendering the patient unable to effectively perceive normal auditory stimuli * Episodes definitively diagnosed as other non-epileptic paroxysmal disorders (such as syncope, paroxysmal kinesigenic dyskinesia, or sleep disorders) * Episodes occurring out of the camera view, obscured, or recorded with poor video quality, preventing accurate assessment of ictal behavioral responses to the clap stimulus * Severe lack of clinical data, loss to follow-up, or refusal/withdrawal of informed consent
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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.
Contacts and locations
Locations
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No.127 Changle West Road, Xincheng District, Xi'an, Shaanxi 710048, China
Shanxi, China
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The First Affiliated Hospital of Air Force Medical University (Xijing Hospital)
Xian, Shanxi, China
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The First Affiliated Hospital of Air Force Medical University (Xijing Hospital)
Shanxi, China
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