Actively Recruiting
Sleepiz One+ vs. Capnography and Electrocardiography
Led by Sleepiz AG · Updated on 2024-08-26
35
Participants Needed
1
Research Sites
10 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Respiratory Rate (RR) and heart rate (HR) are vital signs crucial for assessing a patient's overall health, providing insights into various conditions and stressors. Effective management of chronic diseases relies on detecting pathological changes early, with RR being among the most sensitive predictors of patient deterioration. Therefore, vigilant monitoring of RR and HR is vital for improving patient outcomes. The primary aim of this study is to provide a thorough comparison of the performance of Sleepiz One+ algorithms and end-tidal carbon dioxide measurement (EtCO2) Capnography for measuring respiration rate and electrocardiography (ECG) for measuring heart rate, in healthy adults and patients suffering from chronic conditions (e.g., hypertension, Chronic Obstructive Pulmonary Disease (COPD), asthma, diabetes), at rest in a clinical setting when the data is acquired with the new hardware version. Additionally, the investigators will evaluate the performance of RR estimation against the thoracic effort belt and the HR against the pulse oximetry.
CONDITIONS
Official Title
Sleepiz One+ vs. Capnography and Electrocardiography
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Signed informed consent
- For patients: at least one chronic medical condition such as diabetes, asthma, cardiovascular or respiratory disease
- For healthy volunteers: no diagnosed chronic medical condition
You will not qualify if you...
- Previous participation in this study
- Presence of a cardiac pacemaker or any implanted electrical device
- Women who are pregnant or breastfeeding
- Inability to follow study procedures due to language barriers, psychological disorders, dementia, delirium, or similar conditions
- For healthy volunteers: any diagnosed chronic medical condition
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Schlaflabor Fluntern
Zurich, Canton of Zurich, Switzerland, 8044
Actively Recruiting
Research Team
M
Marta Stepien, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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