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Smart Watch Study for Monitoring Vital Signs

Not Applicable
Conditions
Health Condition 1: R688- Other general symptoms and signs
Registration Number
CTRI/2022/04/041899
Lead Sponsor
GOQii Technologies Pvt Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Participants willing to sign an Informed Consent Form indicating that they understand the purpose of and the procedures required for the study and are willing to participate in it.

2. Male and female patients visiting the out-patient department of the hospital who are of age 18 years and above.

3. Patient having cardiac comorbidity will be considered for enrolment.

Exclusion Criteria

1. Patients who are on ventilator or other life support systems.

2. Patients who have taken any food, drug or other exposed other factors which will influence the blood pressure levels

3. Patients who are allergic to the wearable wrist band materials.

4. Participation in another clinical study concurrently.

5. Any other specific reason which inhibits active participation of the patient in the study as determined by the Investigator.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess accuracy of novel wearable device (GoQii Smart Vital 2.0) for vital sign monitoring (Body Temperature, Blood Pressure, Heart Rate, ECG and Oxygen Saturation (SpO2)) comparing it with conventional readings recorded by digital devices.Timepoint: 0 Hour, 3rd Hour and 6th Hour
Secondary Outcome Measures
NameTimeMethod
ot ApplicableTimepoint: Not Applicable
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