Scientists test new way to track walking issues in rare genetic disorders
NCT ID NCT05161494
First seen May 08, 2026 · Last updated May 16, 2026 · Updated 2 times
Summary
This study tested whether a method for measuring walking problems, originally developed for Dravet syndrome, could also work for people with Tuberous Sclerosis Complex or STXBP1-related epilepsy. Researchers analyzed the walking patterns of 41 participants aged 6 and older using 3D motion capture. The goal was to see if the measurement tools were sensitive enough to detect gait abnormalities in these groups.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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University of Antwerp
Antwerp, 2160, Belgium
Conditions
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