Skip to main content
Clinical Trials/NCT05741931
NCT05741931
Not Yet Recruiting
N/A

Monitoring Pregnant Women Using REST Mobile Application (Risk Identification, Evaluation Counseling, Systematic Monitoring, Troubleshooting)

Gadjah Mada University0 sites216 target enrollmentAugust 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Maternal and Child Health
Sponsor
Gadjah Mada University
Enrollment
216
Primary Endpoint
Reduced incidence of low birth weight babies
Status
Not Yet Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The goal of this Randomized Controlled Trial is to compare the health condition of pregnant women through pregnancy monitoring in the implementation of pregnancy class. The main question it aims to answer are:

How is the condition of the mother and baby after pregnancy monitoring using the REST mobile application (Risk identification, Evaluation counseling, Systematic monitoring, Trobleshooting)

Participants will be monitored for the condition of their pregnancy from 20 weeks of pregnancy until delivery. Participants will attend in the pregnancy class as many as 3 meetings and a pregnancy check-up by the midwife.

Researchers will compare intervention group to see if normal delivery methods, birth weight of the baby (>2500), antenatal care visits (>6 times), and prevention of pregnancy complications were better than the control group.

Detailed Description

The research will involve pregnant women and midwives. The midwife will conduct a pregnancy check-up which includes 10 pregnancy checks (height and weight, blood pressure, upper arm circumference, uterine fundus height, Tetanus immunization, Fe tablets, fetal presentation and fetal heart rate, counseling, laboratory tests, case handling). The examination is carried out every class meeting of pregnant women. The results of the examination will be inputted into the mobile application. Pregnant women will fill in the mobile application if the mother does antenatal care at a health facility. This activity will last until the mother's delivery.

Registry
clinicaltrials.gov
Start Date
August 2023
End Date
December 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Gadjah Mada University
Responsible Party
Principal Investigator
Principal Investigator

Restu Pangestuti

Principal Investigator

Gadjah Mada University

Eligibility Criteria

Inclusion Criteria

  • Pregnant women with a gestational age of 20-22 weeks.
  • Pregnant women who have a pregnancy check-up at a health facility
  • Plan to settle in the research area for at least the next 2 years
  • Willing to participate in the research by signing an informed consent form.

Exclusion Criteria

  • Suffering from chronic diseases that require special pregnancy care
  • It is certain that it cannot give birth normally
  • Unable to operate an android phone

Outcomes

Primary Outcomes

Reduced incidence of low birth weight babies

Time Frame: 20 weeks gestational age until delivery

The baby's birth weight is measured using baby scales and it is expected that the baby's birth weight is more than 2500 grams

Antenatal care for pregnant women more than 6 visits

Time Frame: During pregnancy

Antenatal care by mothers can be measured by the number of visits to health facilities for pregnancy check-ups. Each visit will be recorded on the mobile application starting from the first visit

Reduced incidence of pregnancy complications in the mother

Time Frame: 20 weeks gestational age until delivery

Pregnancy complications are measured using a mobile application by looking at the history of the mother's health condition. Possible complications such as pre-eclampsia, eclampsia, hypertension in pregnancy, and anemia

Increased childbirth by normal methods

Time Frame: 20 weeks gestational age until delivery

The delivery method can be seen using the mobile application in the labor report section. Delivery will be reported by the midwife regarding the method used for childbirth including the results of filling out the partograph

Similar Trials