The DistaSense VITALS Study
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Life Detection Technologies
- Study ID
- NCT07217327
- Status
- Recruiting
Conditions
- Detection of Heart Rate and Respiratory Rate
Eligibility Criteria
- Sex
- ALL
- Age
- 22 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- DistaSense and Polysomnography — DIAGNOSTIC_TESTAll subjects will be evaluated by DistaSense and reference device for respiratory rate and heart rate.
Study Details
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 Dates
- Start date
- Aug 13, 2025
- Status verified
- Sep 2025
- Primary completion
- Nov 30, 2025
- Completion
- Nov 30, 2025
Study Design
- Enrollment
- 20 participants (estimated)
Primary Outcome Measure
Accuracy and bias between the DistaSense measurements of heart rate and respiratory rate and the reference measurements [ Time Frame: Day 1 ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Clayton Sleep Institute | St Louis | Missouri | 63123 | |
| CTI Clinical Research Center | Cincinnati | Ohio | 45212 |