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Your phone could help unlock the mystery of rare muscle paralysis

NCT ID NCT05976958

Summary

This study aimed to test a smartphone app designed to help patients with periodic paralysis, a rare genetic disorder causing sudden muscle weakness attacks. The goal was to see if tracking symptoms like attack frequency, duration, and triggers in real-time on a phone provides more accurate information than trying to remember and report them later at a doctor's visit. Researchers hoped this better data would improve how doctors understand and manage the condition.

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Contacts and locations

Locations

  • RaDiCo-PP

    Paris, Île-de-France Region, 75012, France

Conditions

Explore the condition pages connected to this study.