Walking analysis sheds light on rare genetic disorders
NCT ID NCT05161494
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a special walking test (3D gait analysis) can help identify movement problems in people with rare genetic diseases like Tuberous Sclerosis and STXBP1. About 40 participants aged 6 and older who could walk without help took part. The goal was to see if the test is practical and sensitive enough to measure how their walking differs from normal.
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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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University of Antwerp
Antwerp, 2160, Belgium
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