Health Condition 1: R688- Other general symptoms and signs
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
GOQii Technologies Pvt Ltd
Eligibility
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
Public ContactRitesh Khandelwal
QREC Clinical Research LLP
Outcome results
None listed