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m-Health System for Tracking Kangaroo Mother Care and Temperature in Southern India

Primary Purpose

Preterm Infant, Low Birth Weight Infant, Kangaroo Mother Care

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Wearable device with smart mobile phone
Sponsored by
St. John's Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Preterm Infant

Eligibility Criteria

2 Days - 49 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Stable LBW babies who are less than 2000 grams
  • Kangaroo care provider who could preferably be the mother or any other family member

Exclusion Criteria:

  • Extreme preterm infants (corrected gestational age less than 28 weeks)
  • Any family member who is unwilling to hold the infant in Kangaroo Mother Care position with the wearable device or if presenting with any infection

Sites / Locations

  • St Johns Medical College and Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Wearable device with smart mobile phone

Arm Description

20 mother/care provider-infant pairs practicing Kangaroo Mother Care, from a tertiary super-specialty hospital selected to wear the device ( few days in the hospital and for a week at home when discharged)

Outcomes

Primary Outcome Measures

Evaluation of hypothermia episodes through the wearable device (remote bio-monitoring - RBM) in real world
1. Number of hypothermia (less than 36.5 degree centigrade) episodes
Evaluation of touch through the wearable device (remote bio-monitoring - RBM) in real world
1. No Kangaroo Mother Care ( Skin to skin contact between mother and baby) for 6 hours (alerted through RBM device)

Secondary Outcome Measures

Development of entire computational hardware of the remote bio-monitoring device
No of alert messages from the RBM to project staffs. No of heat map views - total and within 24 hrs. No of responses to failure of normal temperature range (36.5-37 degree centigrade/ Kangaroo Mother Care alerts)

Full Information

First Posted
December 19, 2017
Last Updated
June 28, 2021
Sponsor
St. John's Research Institute
Collaborators
Bill and Melinda Gates Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04929977
Brief Title
m-Health System for Tracking Kangaroo Mother Care and Temperature in Southern India
Official Title
Evaluation of a m-Health System for Tracking Kangaroo Mother Care and Temperature for Providing Feedback to Family Care Givers or Front-line Workers to Enhance Kangaroo Mother Care Adherence
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
March 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. John's Research Institute
Collaborators
Bill and Melinda Gates Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The product innovation is a wearable device that (combined with a smartphone and back-end analytics system) acts as a sensor, processor and actuator, and is therefore designed to identify critical parameters (Kangaroo Mother Care adherence and temperature of neonate on a 24/7 basis and temperature of mother during these episodes), make intelligent and early diagnosis of (persistent or impending) neonatal hypothermia, maternal/neonatal fever and non-adherence to Kangaroo Mother Care and then trigger audio or visual alerts (via the wearable or smart-mobile phone) for action by the care-giver or front-line healthcare worker to enhance Kangaroo Mother Care duration or referral to a health facility as needed.
Detailed Description
Project design and implementation plan: The logic model envisioned in this study as i) wearable sensors, technology design and development with research team personnel as 'inputs'; ii) data analytics deployment with detection of abnormalities as 'processes'; and iii) feedback alerts appraisal as the 'outputs' for this phase of testing. Experimental plan comprises of two steps: a non-clinical phase and a clinical phase. i) The non-clinical phase comprises of the design, development and deployment of the data capture and analytics system. This includes mobile phone app building with features such as push notifications, offline data storage and synchronization on connectivity, local data analysis (with sequentially increasing capabilities as more data comes in) and alerting stakeholders. In addition, capability development of primary nodes for temporary storage and real-time data analysis as also for long-term data storage capabilities that could be scaled to district-level and state-level expansion in future will be done. Data monitoring capacity will be built on real-time visualization dashboards and raising alerts for targeted stakeholders. The entire computational hardware, algorithms/AI engine, network architecture, overall data visualization including heat maps (infrastructure) for this proposed study will be developed by industry experts (will be subcontracted). ii)In the second phase, it is proposed to undertake a technological-feasibility study as a small-scale clinical trial (in a convenient sample of 20 mother-baby pairs) for testing in real-world conditions while the mother-infant pairs are in the hospital for a few days and when they are discharged for follow-up at home for up to a week. This phase will also include a qualitative research component to study acceptability and feasibility of alerting and actionable advisories sent to care-givers and field staff. All data obtained from this program will reside within dedicated servers with storage facilities within the selected hospital from where mother-infant pairs are recruited. Institutional Ethics Committee approval, clinical trial registration and data safety monitoring board constitution will be undertaken to protect human research participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Infant, Low Birth Weight Infant, Kangaroo Mother Care, Hypothermia, Newborn, Fever

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Wearable device combined with a smart mobile phone and back-end analytics system that acts as a temperature and touch sensor and actuator will be evaluated.
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Wearable device with smart mobile phone
Arm Type
Other
Arm Description
20 mother/care provider-infant pairs practicing Kangaroo Mother Care, from a tertiary super-specialty hospital selected to wear the device ( few days in the hospital and for a week at home when discharged)
Intervention Type
Device
Intervention Name(s)
Wearable device with smart mobile phone
Intervention Description
The wearable device will act as a sensor designed to identify critical parameters such as Kangaroo Mother Care adherence and temperature of the infant 24/7 and of the mother-infant pairs during these sessions.
Primary Outcome Measure Information:
Title
Evaluation of hypothermia episodes through the wearable device (remote bio-monitoring - RBM) in real world
Description
1. Number of hypothermia (less than 36.5 degree centigrade) episodes
Time Frame
5 months
Title
Evaluation of touch through the wearable device (remote bio-monitoring - RBM) in real world
Description
1. No Kangaroo Mother Care ( Skin to skin contact between mother and baby) for 6 hours (alerted through RBM device)
Time Frame
5 months
Secondary Outcome Measure Information:
Title
Development of entire computational hardware of the remote bio-monitoring device
Description
No of alert messages from the RBM to project staffs. No of heat map views - total and within 24 hrs. No of responses to failure of normal temperature range (36.5-37 degree centigrade/ Kangaroo Mother Care alerts)
Time Frame
8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Days
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Stable LBW babies who are less than 2000 grams Kangaroo care provider who could preferably be the mother or any other family member Exclusion Criteria: Extreme preterm infants (corrected gestational age less than 28 weeks) Any family member who is unwilling to hold the infant in Kangaroo Mother Care position with the wearable device or if presenting with any infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prem K Mony, MD; MSc-Epi
Organizational Affiliation
St. John's Research Institute, Bangalore 560034
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Johns Medical College and Hospital
City
Bangalore
State/Province
Karnataka
ZIP/Postal Code
560034
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24752403
Citation
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Citation
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PubMed Identifier
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Citation
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Links:
URL
https://www.healthynewbornnetwork.org/blog/energy-independent-appropriate-medical-devices-winding-up-social-innovations-for-newborn-health/
Description
Energy independent appropriate medical devices-winding up social innovations for newborn health

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m-Health System for Tracking Kangaroo Mother Care and Temperature in Southern India

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