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Physiological and Biomarker Monitoring: Enhancing the Vital Signs and Biomarkers Algorithm of Binah.AI in the Kenyan Population.

Physiological and Biomarker Monitoring: Enhancing the Vital Signs and Biomarkers Algorithm of Binah.AI in the Kenyan Population.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202506914478312
Enrollment
1000
Registered
2025-06-04
Start date
2025-08-01
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Circulatory System Nutritional, Metabolic, Endocrine

Interventions

Binah.ai Recorder app

Sponsors

Binah.ai
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The subject must have the ability to understand and provide written informed consent. 2. Male or Female subjects =18 and =65 of age. 3. The subject must be willing and able to comply with study procedures. 4. Subjects with the following co-morbid conditions. Note: Healthy subjects without the following conditions are still eligible i. Subject with Pre-diabetes or diabetes HbA1C 6.4-16% ii. Subject with Hypertension with systolic measurements above 145 mmHg iii. Subject with Total cholesterol with measurements of >240 mg/dl or higher iv. Subjects who are active smokers

Exclusion criteria

Exclusion criteria: 1. The subject has compromised circulation, injury, or physical malformation of fingers, hands, ears or forehead/skull or other sensor Region of Interest (ROI), which would limit the ability to test the ROI needed for the study. Note: Certain malformations may still allow subjects to participate if the condition is noted and would not affect the particular areas utilised. 2. The subject has a tattoo in the optical path, which would limit the ability to conduct the tests needed for the study. 3. Subjects with severe contact allergies to standard adhesives, latex or other materials found in pulse oximetry sensors, respiration monitor electrodes or other medical sensors used for measuring vital signs. 4. Subject with a medical condition which, in the opinion of the investigator, does not allow performing the study assessments. 5. Subject unfit to participate in the study at the judgment of the investigator.

Design outcomes

Primary

MeasureTime frame
Recording of subjects vitals including blood pressure, pulse rate and oxygen saturation using the Binah.ai recorder and reference devices.

Secondary

MeasureTime frame
Blood samples analyses.

Countries

Kenya

Contacts

Public ContactUzodinma Umeh

Chief Medical Officer

uzodinma@zuri.health+2348065741635

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026