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

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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Key information

Conditions

Urinary Tract Infection Acute Otitis Media Arrhythmias, Cardiac Atrial Fibrillation COPD Cardiovascular Diseases Chronic Disease Diabetes Mellitus Disease Attributes Ear Diseases Endocrine System Diseases Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Glucose Metabolism Disorders Healthy Volunteers Heart Diseases Hematologic Diseases Hemic and Lymphatic Diseases Hypertension Infections Iron Deficient Anemia Leukocyte Disorders Leukocytosis Lung Diseases Lung Diseases, Obstructive Male Urogenital Diseases Metabolic Diseases Nutritional and Metabolic Diseases OSA Otitis Otitis Media Otorhinolaryngologic Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms Pneumonia Pulmonary Disease, Chronic Obstructive Respiratory Tract Diseases Respiratory Tract Infections Urinary Tract Infections Urogenital Diseases Urologic Diseases Vascular Diseases

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Oakville Trafalgar Memorial Hospital

Oakville, Ontario, L6M 0L8, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Vitaliti

Device

Primary outcomes

Successful diagnosis of patient's condition by Vitaliti software as compared to patient's Medical Record

Time frame: 90 minutes

Sponsors and collaborators

Lead sponsor

Cloud DX Inc.

Industry

Registry information

Important dates

Study start: 2016
Primary completion: 2017
Study completion: 2017
First posted: Aug 5, 2016
Registry last updated: May 9, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed