Comparison of Resting Heart and Respiratory Rate Measurements Acquired by Contactless Radar Sensors, Electrocardiography, and Capnography

Status unconfirmed

Conditions studied: Vital Signs

In brief

1. Determine agreement (accuracy) of resting heart rate measured by Vitalpercept when compared to an FDA-cleared electrocardiograph (ECG) device, LifeSignals Wireless Biosensor. 2. Determine agreement (accuracy) of resting respiratory rate measured by Vitalpercept when compared to an FDA-cleared capnographer, Capnostream 20.

Key facts

Study ID

NCT04935190

Run by

DawnLight

People needed

100

Starts

2021-06-15

Expected to finish

2021-10-30

Last updated by the study team

2021-08-31

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female subjects ≥ 21 years of age at the time of signing the informed consent.
• Subjects willing to sign the informed consent and capable of committing to the duration of the study.
• Subjects with the ability to lie flat, lie on left side, lie on right side, and sit in a chair.
• Subjects who are able to breathe through their nose for the capnography assessment.
• Subjects that have a diagnosis of a cardiac, pulmonary, or cardio-pulmonary condition (e.g., Congestive Heart Failure, COPD, Asthma) will be assigned to Group 1.
• Subjects who are not known to have a cardiac, pulmonary, or cardio-pulmonary condition will be assigned to Group 2.

You may not qualify if…

• Subjects who are prone to excessive coughing and excessive movement
• Subjects who have a condition that involves uncontrollable movement of the body such as Parkinson's Disease or Essential Tremor.
• Subjects with a history of allergy to adhesive, latex or Nuprep.

Where it is running

• North Carolina Clinical Research — Raleigh, North Carolina, United States

Full record on ClinicalTrials.gov

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