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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-07-31

Study Completion Date

2017-05-31

Brief Summary

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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.

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Detailed Description

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Conditions

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

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Vitaliti System

Vitaliti

Intervention Type DEVICE

Interventions

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Vitaliti

Intervention Type DEVICE

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes