Blood Pressure from Face Video (Vitacam)
Official title: Blood Pressure Measurement Using Vitacam
Run by Evondos Oy · NCT07739667 · Data updated 2026-11-12
A contactless vitals tool called Vitacam tests if video-based blood pressure readings from the face can match standard cuff measurements in adults.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 85 (estimated) |
| Sponsor | Evondos Oy Industry-sponsored |
| Locations | 1 site (Tampere) |
| Status | Recruiting |
| Started | May 11, 2026 |
| Main results expected | September 30, 2026 |
| Study ends | March 31, 2027 |
| Registry record updated | July 31, 2026 |
| Trial ID | NCT07739667 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) who can consent and speak Finnish or English, not pregnant, without other exclusion factors preventing participation.
✕Probably not a fit
Individuals not meeting the criteria or whose measurements fall outside the study’s required distribution may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study collects video-based vital signs to develop and validate a cuffless blood pressure measurement algorithm using Vitacam, a software device that analyzes facial and chest video for remote blood pressure estimation. The study follows EN ISO 80601-2:2019 standards, comparing Vitacam measurements with a clinically validated sphygmomanometer and requiring a diverse sample of at least 85 adults with a distribution of SBP and DBP similar to typical ranges. It uses paired measurements and predefined statistical criteria, including mean differences and standard deviations, to determine accuracy. The goal is to publish validation results in peer review literature.
Why it matters
Potential benefit: If successful, Vitacam could offer a non-contact way to estimate blood pressure in adults.
How similar studies have gone: Prior research has used cuffless, video-based methods with mixed success; this trial contributes validation under ISO standards.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18 years or older * Ability to give informed consent * Volunteering for the study * Fluent Finnish or English Exclusion Criteria: * Age under 18 years * Pregnancy * Inability to give informed consent * Denial
Where it's running
-
Tampere University
Tampere, Finland Recruiting
Study contacts
- Principal investigator: Antti Vehkaoja — Tampere University
- Study coordinator: Moyeen Ahmad
- Email: moyeen.ahmad@evondos.com
- Phone: +35850486879
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Inflation-based non-invasive blood pressure test compared with standard cuff method
This study tests whether the Philips iNIBP device gives BP readings that match the usual auscultatory cuff method in people aged 3 to 85.
-
Automated Non-Invasive Blood Pressure: Tracking Blood Pressure Changes Using SpO2 Data
This study tests an algorithm that estimates blood pressure changes using data from an SpO2 sensor in patients in the OR, PACU, or ICU who already have invasive BP measured as part of standard care.
-
NIBP Accuracy Validation in Adults
This study tests how accurately a non-invasive blood pressure device measures blood pressure in adults by comparing it with arterial line readings.
-
New Non-Invasive Blood Pressure (NIBP) Enhancement for Neonates and Children
This study tests a new NIBP device enhancement in neonates and kids to see if it can measure blood pressure more accurately.
-
Non-invasive blood pressure accuracy study for adults
This study tests whether non-invasive blood pressure readings match invasive aortic pressure measurements in adults who need arterial line monitoring.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.