The DistaSense VITALS Study

Recruiting now

Conditions studied: Detection of Heart Rate and Respiratory Rate

In brief

A prospective, non-significant risk study designed to validate the performance of the DistaSense Contactless Sensor and algorithm for detecting heart rate and respiratory rate, compared to gold standard reference technology.

Key facts

Study ID

NCT07217327

Run by

Life Detection Technologies

People needed

20

Starts

2025-08-13

Expected to finish

2025-11-01

Last updated by the study team

2025-11-03

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Age ≥ 22 years
• Fluent in English
• Willing and cognitively able to provide informed consent
• BMI < 36
• Expected by the investigator to achieve sufficient sleep duration for a minimum of 4 hours of meaningful data (e.g., absence of significant insomnia)
• Able to complete the scripted portion of the evaluation

You may not qualify if…

• Pregnant
• Sufficiently broken, damaged or irritated skin or rashes near the sensor application sites such that investigator believes should be precluded from enrollment
• Subjects with electronic implants of any kind (e.g. pacemaker)
• Subjects that are Life Detection Technology employees or shareholders, or family of a Life Detection Technology employee or shareholder

Where it is running

• Clayton Sleep Institute — St Louis, Missouri, United States (enrolling)
• CTI Clinical Research Center — Cincinnati, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

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