A Decentralized Study to Evaluate Physical Activity and Cough Frequency Using Wearable Technology in Cystic Fibrosis
Completed
Conditions studied: Cystic Fibrosis
In brief
This study will evaluate the performance of wearable technology in cystic fibrosis (CF) participants taking commercial Elexacaftor (ELX)/Tezacaftor (TEZ)/Ivacaftor (IVA) utilizing a fully decentralized trial design.
Key facts
- Study ID
- NCT04923464
- Run by
- Vertex Pharmaceuticals Incorporated
- People needed
- 51
- Starts
- 2021-06-30
- Expected to finish
- 2021-12-20
- Last updated by the study team
- 2022-01-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- National Jewish Health — Denver, Colorado, United States
- Yale New Haven Hospital — New Haven, Connecticut, United States
- Central Florida Pulmonary Group, P.A. — Orlando, Florida, United States
- Children's Hospital of Illinois at OSF Saint Francis Medical Center, Cystic Fibrosis Center — Peoria, Illinois, United States
- Massachusetts General Hospital Cystic Fibrosis Center Clinical Rsearch Center — Boston, Massachusetts, United States
- Washington University School of Medicine — St Louis, Missouri, United States
- Morristown Medical Center — Morristown, New Jersey, United States
- Mount Sinai Beth Israel — New York, New York, United States
- Santiago Reyes, M.D. — Oklahoma City, Oklahoma, United States
- UPMC Children's Hospital of Pittsburgh — Pittsburgh, Pennsylvania, United States
- UW School of Medicine & Public Health — Madison, Wisconsin, United States
- Birmingham Heartlands Hospital — Birmingham, United Kingdom
- Royal Devon and Exeter Hospital — Exeter, United Kingdom
- St. James University Hospital — Leeds, United Kingdom
- Royal Brompton & Harefield NHS Foundation Trust, Royal Brompton Hospital — London, United Kingdom
- Wythenshawe Hospital — Manchester, United Kingdom
- Southampton General Hospital — Southampton, United Kingdom
Full record on ClinicalTrials.gov
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