Study to Compare Two Methods of Measuring Breathing Rates
Respiration Measured Via End-tidal CO2 and Spirometry Study (RESPI)
Recruiting
Observational Study
Respiration Rate Detection
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
50 (estimated)
Sponsor
Boston Scientific Corporation · Industry
Who this trial is looking for
This trial is looking for people who are at least 18 years old and work as BSC employees. Participants will help collect breathing data using two different methods to see how they compare.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years old or older.
I work full time or part time as a BSC employee.
I can provide informed consent.
I am willing to participate in the required testing.
You may not be able to join if
I am currently enrolled in another clinical trial.
I am pregnant.
I have a known allergy to Neoprene or Nylon.
I have a past or current medical event that could pose a risk.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
To collect respiration data via end-tidal CO2 and spirometry and compare respiration rates measured via the two methods.
Trial Locations
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City
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Status
Eligibility Criteria
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 plac…
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
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