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The Effect of e-Registration and mHealth on Institutional Deliveries in the Hazard-prone Areas

The Effect of e-Registration and mHealth on Institutional Deliveries in the Hazard-prone Areas of Southern Bangladesh: A Protocol for an Open-label Two-arm Non-randomized Controlled Cluster Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05398978
Enrollment
536
Registered
2022-06-01
Start date
2022-06-01
Completion date
2022-11-30
Last updated
2022-06-01

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

Conditions

Place of Delivery

Keywords

Non-randomized controlled cluster trial; institutional delivery; e-Registration; mHealth

Brief summary

The study aims to determine the effect of the eRegistration tracking system and mHealth counseling on institutional deliveries to pregnant mothers in the hazard-prone areas of Southern Bangladesh.

Detailed description

The study will be an open-label two-arm non-randomized controlled cluster trial for six months period. Chandpur Sadar, Kachua, and Faridganj sub-districts will be the intervention arm and Bhola Sadar, Charfesson, and Lalmohan sub-districts of the Bhola district will be the control arm. ased system. 28 - 36 weeks of pregnant women will be enrolled, given the intervention, and followed-up until their delivery.

Interventions

OTHERe-Registration and mHealth

Registration to the electronic database Counseling through voice calls for facility delivery Text messages to promote facility delivery

Sponsors

International Centre for Diarrhoeal Disease Research, Bangladesh
CollaboratorOTHER
North South University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

The pregnant mothers will be registered in the electronic database, they will be called by the midwives to motivate them for facility delivery and they will receive a text message regarding this.

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

Pregnant mothers registered in the FWA register, 19 - 45 years, 28 - 36 weeks pregnant, have access to a mobile phone

Design outcomes

Primary

MeasureTime frameDescription
Rate of Institutional delivery22 weeksNormal vaginal deliveries, cesarean sections and assisted vaginal deliveries (forceps and vacuum deliveries) conducted at any healthcare facility by medically trained provider/ skilled birth attendant situated at the study sites will be considered as institutional delivery. Numerator: Number of institutional deliveries Denominator: Total deliveries in the study sites (A sum of normal vaginal deliveries, cesarean sections and assisted vaginal deliveries)

Secondary

MeasureTime frameDescription
Proportion of different mode of deliveries22 weeksNumerator: Proportion of normal vaginal deliveries, Proportion of cesarean sections, Proportion of forceps and vacuum deliveries Denominator: Total deliveries in the study sites.
Proportion of different birth outcomes22 weeksNumerator: Proportion of alive babies, Proportion of stillbirths Denominator: Total live births in the study sites.

Contacts

Primary ContactAhmed Hossain, Ph.D, MSc
ahmed.hossain@northsouth.edu+8801729378236

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026