Actively Recruiting
The DistaSense VITALS Study
Led by Life Detection Technologies · Updated on 2025-11-03
20
Participants Needed
2
Research Sites
11 weeks
Total Duration
On this page
Sponsors
L
Life Detection Technologies
Lead Sponsor
N
Nilo Medical Consulting Group
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The DistaSense VITALS Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 22 years or older
- Fluent in English
- Willing and cognitively able to provide informed consent
- Body mass index (BMI) less than 36
- Expected to sleep for at least 4 hours to provide meaningful data
- Able to complete the scripted evaluation portion
You will not qualify if you...
- Pregnant
- Broken, damaged, or irritated skin or rashes near sensor sites
- Having electronic implants such as pacemakers
- Employees, shareholders, or family of employees or shareholders of Life Detection Technology
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Clayton Sleep Institute
St Louis, Missouri, United States, 63123
Actively Recruiting
2
CTI Clinical Research Center
Cincinnati, Ohio, United States, 45212
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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