Respiration Measured Via End-tidal CO2 and Spirometry Study (RESPI)
Purpose
To collect respiration data via end-tidal CO2 and spirometry and compare respiration rates measured via the two methods.
Condition
- Respiration Rate Detection
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Willing and able to provide informed consent - Age 18 or above - Full time or part time BSC employee - Willing and able to participate in the required testing
Exclusion Criteria
- Currently enrolled in another clinical trial that might interfere with data collection or placement of the study system - Subject is pregnant as indicated by subject report - Known allergy or sensitivity to materials used in the study (Neoprene, Nylon) - Any past or current medical event that could represent a risk for the subject to perform the study required activities in the opinion of the investigator
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Wearable respiration mask | Healthy control subjects not eligible for exercise. |
|
| Wearable respiration mask - Exercise | Healthy control subjects eligible for exercise. |
|
Recruiting Locations
Boston Scientific Arden Hills
Saint Paul, Minnesota 55014
Saint Paul, Minnesota 55014
More Details
- NCT ID
- NCT07537478
- Status
- Recruiting
- Sponsor
- Boston Scientific Corporation
Detailed Description
This is a non-randomized, data collection study that will enroll up to 50 participants. There will be one study visit per participant and no follow up period.