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Phone app aims to better track rare muscle paralysis attacks

NCT ID NCT05976958

First seen Mar 09, 2026 · Last updated Jun 12, 2026 · Updated 20 times

Summary

This study tested a smartphone app designed to help people with periodic paralysis—a rare genetic condition causing sudden muscle weakness—track their episodes in real time. The goal was to see if using the app gives doctors more accurate information about attack frequency, duration, and triggers compared to standard in-clinic interviews. Only 2 participants were enrolled before the study ended early, so results are limited.

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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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Contacts and locations

Locations

  • RaDiCo-PP

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

Conditions

The condition(s) this trial relates to.

periodic paralysis Rare Diseases

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.