Study reveals hidden differences in Kids' lung diseases during exercise

NCT ID NCT07157644

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study looked at 88 children with cystic fibrosis (CF) or primary ciliary dyskinesia (PCD) to compare how well they can exercise, how their muscles use oxygen, and how strong their breathing muscles are. Researchers used walking tests and muscle oxygen monitors to measure these factors. The goal was to better understand the differences between these two genetic lung diseases, which both cause breathing problems and limit physical activity.

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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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Conditions

The condition(s) this trial relates to.

cystic fibrosis Motor Activity primary ciliary dyskinesia

As listed by the trial registrant

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

Contacts and locations

Locations

  • Gazi University Faculty of Health Sciences Department of Cardiopulmonary Physiotherapy and Rehabilitation

    Ankara, Çankaya, 06490, Turkey (Türkiye)