Wearable tech tracks if new CF drug helps patients breathe easier and move more
NCT ID NCT04969224
Summary
This study tested how well a three-drug combination (elexacaftor/tezacaftor/ivacaftor) works for people with cystic fibrosis. It specifically measured if the treatment could reduce daily coughing and increase physical activity in patients aged 12 and older. Researchers used wearable technology to track participants' coughs and step counts over several weeks.
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Contacts and locations
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Locations
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Alfred Hospital
Melbourne, VIC, Australia
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Cliniques Universitaires de Bruxelles Hopital Erasme
Brussels, Belgium
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Corporacio Sanitaria Parc Tauli - Sabadell Hospital Universitari
Sabadell, Spain
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Hospital Universitari Vall d Hebron
Barcelona, Spain
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Hospital Universitario 12 de Octubre
Madrid, Spain
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Hospital Universitario Ramon y Cajal
Madrid, Spain
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Institute for Respiratory Health
Nedlands, Australia
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Mater Adult Hospital
South Brisbane, Australia
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Queen Elizabeth II Health Sciences Center
Halifax, Canada
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Queensland Children's Hospital
South Brisbane, Australia
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Royal Adelaide Hospital
Adelaide, Australia
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Telethon Kids Institute
Nedlands, Australia
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The Prince Charles Hospital
Chermside, Australia
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The Royal Children's Hospital
Parkville, VIC, Australia
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Universitair Ziekenhuis Brussel - Campus Jette
Brussels, Belgium
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Universitair Ziekenhuis Gent
Ghent, Belgium
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Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg
Leuven, Belgium
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University of Alberta Hospital, Edmonton Clinic
Edmonton, Canada
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University of Calgary Medical Clinic of the Foothills Medical Centre
Calgary, Canada
Conditions
Explore the condition pages connected to this study.