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High Risk Pregnancy Monitoring using Mobile Phones

Mobile obstetrical Monitoring - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2013/03/003501
Enrollment
105
Registered
2013-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- High Risk Pregnancy

Interventions

None listed

Sponsors

Philips Electronics India Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant Ladies 1. The age of the subjects should be at least 18 years or more. 2. The subjects should be registered with the hospital for antenatal care (ANC) 3. Subjects should be citizen of India by descent Healthcare Workers 1. The healthcare workers (ASHAs, ANM and doctors) for this study will be recruited by the PI. These healthcare workers should already be a part of the existing PHC, Suttur, or JSS medical college hospital, Mysore. 2. They should know English. 3. ASHAs and ANM recruited for the study should know how to operate a mobile phone.

Exclusion criteria

Exclusion criteria: Pregnant Ladies 1. The subjects under 18 years of age 2. The subject not registered at hospital for ANC care 3. The subject is not a citizen of India by descent Healthcare Workers 1. The subjects under 18 years of age For the pregnant ladies. Data will be collected non-invasively and automatically by approved medical devices. Data not available electronically (Weight, Height, Blood Pressure) will be manually entered into the Mobile for completeness of the patient case study

Design outcomes

Primary

MeasureTime frame
To get qualitative feedback from doctors and community health workers on workflow and usability aspect of the proposed MoM solution and compare them to the existing system to quantify the benefits of the proposed solution. The feedback of doctors and community health workers will be recorded using questionnaires and interviews.Timepoint: Completion of Questionnaires

Secondary

MeasureTime frame
To test the technical feasibility of implementation of our prototype solution in existing healthcare infrastructure. This will help in accessing the technical feasibility of this proposed m-health solution in the obstetric space.Timepoint: Time at which the complete data transfer from Primary Health Center to Tertriary Care Hospital

Countries

India

Contacts

Public ContactDr Sujit Hiwale

Philips Research India - Bangalore

sujit.hiwale@philips.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026