Skip to content
Trial Eligibility
Menu

The DistaSense VITALS Study

NCT07217327

This study is recruiting at 2 US sites in 2 states, according to its ClinicalTrials.gov record last updated .

Summary

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Detection of Heart Rate and Respiratory Rate

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
22 years and older
Sex
All
Healthy volunteers
Accepted
Sponsor
Life Detection Technologies
Last updated on ClinicalTrials.gov
November 3, 2025

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Missouri · 1

  • Clayton Sleep Institute · St Louis, MO

Ohio · 1

  • CTI Clinical Research Center · Cincinnati, OH

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.