Preliminary Testing of the Vitaliti CVSM Wearable, Vitaliti Spirotoscope, and Vitaliti IVD Station

Cloud DX

Status: Completed

Conditions: Leukocytosis; Hypertension; Healthy Volunteers; Acute Otitis Media; Atrial Fibrillation; Urinary Tract Infection; Iron Deficient Anemia; Diabetes Mellitus; Pneumonia; COPD; OSA

Treatments: Device: Vitaliti

Study type: Observational

Funder types: Industry

Identifiers

NCT02856633

STP-VIT-001

Details and patient eligibility

About

The study objective is to satisfy the testing requirements for the Qualcomm Tricorder XPRIZE Competition. This requires an oversight model using the Vitaliti CVSM Wearable, Vitaliti Spirotoscope, and Vitaliti IVD Station to continuously monitor the patient's five core vital signs and to detect the health conditions required by the competition.

Enrollment: 40 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age 18 to 65 years of age.
• English speaking
• Established diagnosis of one of the thirteen required conditions with evidence in Medical Record.

Exclusion criteria

• Lack of patient consent
• Has pacemaker or internal medical device
• Pregnancy
• Concurrent enrollment into a clinical trial that may affect subject treatment
• Age less than 18 or over 65
• Physical disabilities affecting vision (eyeglasses or contact lenses will be allowed), manual manipulation, or use of a computer or mobile device

Trial design

40 participants in 1 patient group

Vitaliti System

Treatment:

Device: Vitaliti