| CTRI Number |
CTRI/2021/12/038849 [Registered on: 22/12/2021] Trial Registered Prospectively |
| Last Modified On: |
12/04/2023 |
| Post Graduate Thesis |
No |
| Type of Trial |
Observational |
|
Type of Study
|
Cross Sectional Study |
| Study Design |
Single Arm Study |
|
Public Title of Study
|
Non-contact vitals monitoring |
|
Scientific Title of Study
|
Contactless Monitoring Of Body Vitals Using Ballistocardiogram |
| Trial Acronym |
|
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Sharanu Patil |
| Designation |
Head of Department Anesthesiology |
| Affiliation |
Sparsh Hospital Bangalore |
| Address |
Department of Anesthesia First Floor
Sparsh Hospital,
29/P2,The health city Bommasandra Industrial Area,
Hosur Road
Bangalore
Bangalore KARNATAKA 560099 India |
| Phone |
|
| Fax |
|
| Email |
drsharanupatil@sparshhospital.com |
|
Details of Contact Person Scientific Query
|
| Name |
Pooja Kadambi |
| Designation |
Head, Innovation and Clinical Research |
| Affiliation |
Turtle Shell Technologies |
| Address |
Turtle Shell Technologies City Centre, 40, Ground & Mezzanine flr,
Nomads Daily Huddle, Chinmaya Mission Hospital Rd, Indiranagar,
Bengaluru, Karnataka
Bangalore KARNATAKA 560038 India |
| Phone |
|
| Fax |
|
| Email |
pooja@dozee.io |
|
Details of Contact Person Public Query
|
| Name |
Pooja Kadambi |
| Designation |
Head, Innovation and Clinical Research |
| Affiliation |
Turtle Shell Technologies |
| Address |
Turtle Shell Technologies City Centre, 40, Ground & Mezzanine flr,
Nomads Daily Huddle, Chinmaya Mission Hospital Rd, Indiranagar,
Bengaluru, Karnataka
Bangalore KARNATAKA 560038 India |
| Phone |
|
| Fax |
|
| Email |
pooja@dozee.io |
|
|
Source of Monetary or Material Support
|
| Sparsh Hospital Room number 10, Ground floor OPD,Prestige Opal
Sparsh Hospital
#146 Infantry Road Opposite to police commissioners office
Bangalore 560001
|
|
|
Primary Sponsor
|
| Name |
Turtle Shell Technologies Private Limited |
| Address |
City Centre, #40, Ground & Mezzanine flr, Nomads Daily Huddle, Chinmaya Mission Hospital Rd, Indiranagar, Bengaluru, Karnataka 560038 |
| Type of Sponsor |
Other [Medical Device] |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Soujanya Wilson |
Sparsh Hospital Infantry Road |
Room number 10, Ground floor OPD,Prestige Opal
#146 Infantry Road Opposite to police commissioners office
Bangalore 560001
Department of Anesthesia First Floor
Sparsh Hospital,#29/P2,The health city Bommasandra Industrial Area,
Hosur Road
Bangalore 560099
Bangalore KARNATAKA |
9606197707
soujanya@sparshhospital.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| Sparsh Hospital Ethics Committee |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Healthy Human Volunteers |
Screening for Heart Rate, Respiratory Rate and Oxygen Saturation |
|
|
Intervention / Comparator Agent
|
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
90.00 Year(s) |
| Gender |
Both |
| Details |
1. Adults (Above 18 years of age)
2. Provide written informed consent
3. Weight (Above 40 kgs)
4. Are located in a non-ICU hospital setting
5. Agree and able to not eat during the testing period
6. Agree and able to to keep still |
|
| ExclusionCriteria |
| Details |
1. Are connected to a device which may interfere with the device monitoring in this study,
eg. Airbeds
2. A likely need to receive or undergo a procedure/care during the testing period
3. Have a pacemaker or defibrillator
4. Cannot accept a nasal cannula, or have a monitor lead placed on the chest
5. A significant medical condition in the judgement of the investigator, which may
compromise the study testing procedures |
|
|
Method of Generating Random Sequence
|
Not Applicable |
|
Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
1. Root mean square deviation (RMSD) of the Dozee’s HR and Gold Standard Devices
HR
â—‹ Simultaneously record HR in both devices and calculate and compare the
RMSD per patient and the Bland-Altman Plot
2. Root mean square deviation (RMSD) of the Dozee’s RR and Gold Standard Devices
RR
â—‹ Simultaneously record RR in both devices and calculate and compare the
RMSD per patient and the Bland-Altman Plot
3. Root mean square deviation (RMSD) of the Dozee’s SpO2 and Gold Standard Devices
SpO2
â—‹ Simultaneously record SpO2 in both devices and calculate and compare the
RMSD per patient and the Bland-Altman Plot |
At Baseline |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| NIL |
Not Applicable |
|
|
Target Sample Size
|
Total Sample Size="100" Sample Size from India="100"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
03/01/2022 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="0" Months="6" Days="0" |
Recruitment Status of Trial (Global)
Modification(s)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Closed to Recruitment of Participants |
|
Publication Details
|
NIL |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Heart Rate (HR), Respiration Rate (RR), and Oxygen Saturation (SpO2) are the most common vital signs used by medical professionals to monitor health of the patients. While a pulse oximeter is mostly used only to capture oxygen saturation, it can also be used to measure heart rate, though ECG remains the gold standard for heart rate measurement. Respiration, on the other hand, is traditionally measured manually by the nursing staff but can also be measured using a nasal thermistor or capnography. Monitoring of these vitals with less cumbersome techniques would be ideal in long term monitoring of patients and healthy people to detect any sudden abnormalities and long-term health deterioration. During COVID-19 pandemic, remote monitoring devices have come up as champions to assist the healthcare workers in patient monitoring. Several advancements have been made in achieving continuous long-term monitoring of vitals using wrist watches, PPG sensors, etc. [1, 2]. But very few of these have been implemented with acceptable accuracy. The Dozee device developed by Turtle Shell Technologies Pvt. Ltd., is a non-contact continuous vital parameters monitoring system. It is designed for continuous and contactless measurement of HR HR, RR, and SpO2 (when connected with an accessory). The device uses the concept of ballistocardiography and deploys piezoelectric sensors to capture the micro-vibrations originating from cardiac contractions, upper respiratory tract activity and body movements. This data is then analyzed by a proprietary algorithm and the values of the vital parameters – HR and RR are generated. The sensor sheet is placed below the mattress and captures data while the user is resting or sleeping and does not require a sensor to be fixed to the body making it ideal when compared to current methods. Monitoring people’s vital signs outside an ICU often relies on nursing staff conducting checks at set intervals. The device can reduce the workload for nursing staff in non-ICU wards. This device is intended to be used to monitor individuals/patients greater than eighteen years of age (40 kg ≤ weight ≤ 120 kg) and can measure their vital signs during sleep and resting state. The data can be viewed on the dashboard, exported, and even be directly transferred to the in-house hospital management software. This protocol aims at verifying the effectiveness of the investigational device in a general-care clinical environment. References 1. Etiwy M, Akhrass Z, Gillinov L, et al. Accuracy of wearable heart rate monitors in cardiac rehabilitation [published correction appears in Cardiovasc Diagn Ther. 2020 Jun;10(3):644-645]. Cardiovasc Diagn Ther.2019;9(3):262-271. doi:10.21037/cdt.2019.04.08 2. Charlton PH, Bonnici T, Tarassenko L, Clifton DA, Beale R, Watkinson PJ. An assessment of algorithms to estimate respiratory rate from the electrocardiogram and photoplethysmogram. Physiol Meas. 2016;37(4):610-626. doi:10.1088/0967-3334/37/4/610
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