Detection of change in respiratory rate in adult patients with cystic fibrosis during inpatient treatment for a pulmonary exacerbation. Respiratory
Conditions
Interventions
Following study consent, participants will have respiratory rate and related respiratory metrics (including respiratory rate variability, duration of inhalation and exhalation, ratio between respirati
Sponsors
Royal Papworth NHS Foundation Trust
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Clinical diagnosis of Cystic Fibrosis and confirmed by genetic testing 2. Age >= 18 years of age at time of consent 3. Able to provide written informed consent 4. Admitted to Royal Papworth Hospital to receive treatment for a pulmonary exacerbation 5. Already using the Project Breathe remote monitoring kit
Exclusion criteria
Exclusion criteria: 1. Patients unable to provide written informed consent 2. Lung transplant recipients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in mean respiration rate (breaths per minute) during admission day 1 to day 14. The ward nurses will measure respiration rate by counting how many times the participants chest rises in a minute. This information will then be documented in the medical notes. | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in respiratory rate variability using breaths per minute over day 1 to 14. The ward nurses will measure respiration rate by counting how many times the participants chest rises in a minute. This information will then be documented in the medical notes. | — |
Countries
England, United Kingdom
Outcome results
None listed