Pregnancy Monitoring Using Mobile Application

Gadjah Mada University

Status: Not yet enrolling

Conditions: Maternal and Child Health

Treatments: Device: mobile application REST (Risk identification, Evaluation counseling, Systematic monitoring, Troubleshooting)

Study type: Interventional

Funder types: Other

Identifiers

NCT05741931

485838

Details and patient eligibility

About

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.

Full 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.

Enrollment: 216 estimated patients

Sex: Female

Ages: 20 to 35 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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216 participants in 2 patient groups

Intervention Group

Experimental group

Description:

Pregnant women and midwives will use the REST (Risk identification, Evaluation counseling, Systematic monitoring, Troubleshooting) mobile application to monitor the condition of maternal pregnancy. Mothers and midwives will implementation 3 times of pregnancy class until mothers give birth

Treatment:

Device: mobile application REST (Risk identification, Evaluation counseling, Systematic monitoring, Troubleshooting)

Control Group

No Intervention group

Description:

Pregnant women and midwives will conduct pregnancy monitoring as usual. The pregnancy class will be implemented in accordance with government program standards. Mothers will take pregnancy class 3 times until the mother gives birth