Development of Mobile Application Based Breastfeeding Education Program and Evaluation of the Program Effectiveness

August 9, 2022 updated by: ZEHRA ACAR, Istanbul University - Cerrahpasa (IUC)

Purpose of Research: The purpose of this research is to develop and evaluate the effectiveness of a mobile application-based breastfeeding education program.

Research Hypotheses H1: Exclusive breastfeeding rate is higher for mothers in the experimental group than the mothers in the control group in the fourth postpartum week.

H2: The mothers in the experimental group had higher scores on the Evaluation of Breastfeeding Problems in the fourth week after delivery than the mothers in the control group.

H3: Exclusive breastfeeding rate is higher for the mothers in the experimental group than the mothers in the control group in the eighth postpartum week.

H4: The mothers in the experimental group had higher scores on the Evaluation of Breastfeeding Problems at the eighth postpartum week than the mothers in the control group.

In the first stage of the research, a mobile application-based breastfeeding education program was developed and piloted. In the second stage of the study, the mobile application-based breastfeeding education program was applied to the primiparous mothers in the experimental group for eight weeks, starting from the first day of postpartum.The control group received only routine health care.

617 / 5.000 Çeviri sonuçları Personal Information Form, Breastfeeding Evaluation Scale and Breastfeeding Problems Evaluation Scale were applied to the mothers in the Experimental and Control groups on the first postpartum day.

  • A mobile application was installed on the phones of the mothers in the experimental group and information was provided. The control group benefited only from routine nursing care.
  • Infants' Physical Development Monitoring Form, Breastfeeding Monitoring Form, Breastfeeding Problems Evaluation Scale will be applied to the mothers in the experimental and control groups in the fourth and eighth weeks postpartum.
  • Mobile Application Evaluation Form was also applied to the experimental group in the eighth week.

Study Overview

Status

Active, not recruiting

Detailed Description

The research consists of two stages. In the first stage, the mobile application was developed and a pilot application was made with 6 mothers in the testing of the application. For the second stage of the research, all primiparous mothers in Istanbul University Cerrahpaşa Medical Faculty Hospital between September 2021 and August 2022 constituted the population of the research. The sample of the study consisted of primiparous mothers who met the inclusion criteria and volunteered to participate in the study. The sample of the study formed the Experiment and Control group. Primiparous mothers in the experimental group were included in the mobile application-based breastfeeding education program, and the primiparous mothers in the control group were not included in this program and only benefited from the hospital's routine care services (Figure 1.) Power analysis was performed using the G-Power program to determine the number of samples. According to Cohen's effect size coefficients; According to the calculation made by assuming that the evaluations to be made between two independent groups will have a large effect size (d=0.8), when α: 0.05 and 90% power are taken, there should be at least 34 people for each group, considering the losses that may occur during the research process. A total of 80 primiparous mothers, 40 for one group, were planned to be included in the study..

The research consists of two stages. The first stage of the research consists of creating the information content of the mobile application-based breastfeeding education program, developing the application and making the pilot application. In the second stage of the study, primiparous mothers in the experimental group were included in the mobile application-based breastfeeding education program, while the mothers in the control group were not included in any practice other than routine nursing care. Data from mothers in the experimental and control groups were collected on postpartum first day, fourth week, and eighth week.

The first stage of the research Creating the content of the mobile application-based breastfeeding program In the first stage of the research, the content of the mobile application-based breastfeeding program was prepared in line with the literature. Presenting the content of the program on a scientific basis and the measurement and evaluation of education/programs in the world are now stated as an important criterion of evidence-based studies. For this reason, the content of the application was prepared with reference to the current sources of "World Health Organization" and "Ministry of Health". After the content was prepared, the development process of the mobile application was started.

Development of a mobile application-based breastfeeding program The development of the mobile application consists of six main stages: design, development, testing, reporting, maintenance and deployment. Design phase; It consists of evaluating the requirements analysis, considering the User Interface (UI) and user experience (UX) standards, printing the design as Mock-Up and submitting it for approval, and revising it in line with the data notifications. Development phase; development in line with the approved design, interaction via cloud (Cloud) service (Firebase), and development of the application on Cross-Platform as IOS and Android. Development phase; development in line with the approved design, interaction via cloud (Cloud) service (Firebase), and development of the application on Cross-Platform as IOS and Android. Development phase; development in line with the approved design, interaction via cloud (Cloud) service (Firebase), and development of the application on Cross-Platform as IOS and Android. Test phase; It consists of preparing the pilot-test environment, producing the IPA for the IOS version, producing the APK file for Android and conducting development tests. Reporting phase; consists of reporting and sharing the information received from the user. Maintenance phase; In the testing process, it consists of the process of making adjustments and improvements in the application in line with the feedback. The last stage, the distribution stage, is; It consists of obtaining certificates for Android and Apple, preparing necessary images for Android and Apple market environment, obtaining distribution approval by Apple and Android and uploading them to Apple and Android Market. In this direction, first of all, a special logo was designed for the application. Afterwards, the prepared content was integrated into the application. By clicking on the sign up tab at the first login of the application, an e-mail and password were created and the login application was registered, and the next login was made automatically. The information page of the application contained brief information about the application and three pages on the importance of breastfeeding and breast milk. Afterwards, information about the mother's name, baby's name, baby's gender and baby's birth weight was filled and the application was entered. These two screens were reserved for the first entry only. The main screen of the application used to be six screens. These six screens; Breastfeeding, Expressing, Contingencies, Frequently asked questions and my Breastfeeding Log and Breastfeeding diary. Mothers could record the number and duration of breastfeeding, milking status, the baby's height and weight, if it was a measure, the breastfeeding problem and solutions they encountered, on the "Breastfeeding Introduction" tab, and they could follow their breastfeeding status in the "Breastfeeding Diary" tab. In addition, notifications were sent once at the first entry to the application, and then 2-3 times a week to increase the breastfeeding motivation of the mothers.

The notification sent on the first login to the application; "Dear mom, your breastfeeding journey has begun. In this process, you can access the information you need through the application, keep a diary at the breastfeeding entrance and follow the breastfeeding process…"

Making a pilot application With the development of the application, the pilot application was started. Six mothers who met the inclusion criteria were included. The link of the application was sent to Android-operated phones via google drive in order to prevent sharing, and application invitation mail was sent to IOS-operated phones, application registrations were made through the app store, and the application was accessed by entering the code via the "Test Flight" application.

Mothers expressed the progress error on the breastfeeding home page, this technical issue was edited by the mobile application developer. In addition, mothers stated that they can have videos in the application and that receiving notifications will ensure the continuity of breastfeeding login. With these suggestions, the papers were systematized. No video is included in the application as it may negatively affect the usability of the application.

Second phase of the research In the second stage of the study, mothers who met the criteria for inclusion in the sampling were informed about the purpose, content and method of the study, and informed consent was obtained from the mothers who agreed to participate in the study. Following the CONSORT 2017 (Updated Guidelines for Reporting Randomized Parallel Group Studies) report, mothers were randomly assigned to the Experiment and Control groups using a simple random numbers table on https://www.random.org/integers/. Personal Information Form, Breastfeeding Evaluation Scale and Breastfeeding Problems Evaluation Scale were applied to the mothers in the Experimental and Control groups on the first postpartum day. The mobile application was installed on the phones of the mothers in the experimental group and they were informed about the content and use of the application. The control group benefited only from routine nursing care. Infants' Physical Development Monitoring Form, Breastfeeding Monitoring Form, Breastfeeding Problems Evaluation Scale were applied to the mothers in the experimental and control groups in the fourth and eighth weeks postpartum. The baby's weight, height and head circumference, which was included in the Baby's Physical Development Monitoring Form, was measured at the "Family Health Center". Due to the reduction of the difference between the measurements, the babies were asked to be weighed with clean diapers and without clothes. The mothers who had difficulty in filling out the questions online were contacted by the researcher and they were asked to read and answer the questions. In addition, the Mobile Application Evaluation Form was applied to the experimental group in the eighth week.

Study Type

Interventional

Enrollment (Actual)

73

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Istanbul University-Cerrahpasa

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • 18 years or older,
  • Primiparous,
  • Babies born at term (> 37 weeks of pregnancy or weight > 2500 g) and no health problems that prevent suckling
  • Planning to breastfeed,
  • Having a smart phone and effective usage skills,
  • Mothers who agreed to participate in the study for eight weeks were included in the sample.

Exclusion Criteria:

  • Being the first born,
  • Having multiple pregnancy,
  • Having a physical and/or mental health problem
  • Having a risky newborn,
  • Having a history of breast surgery or breast reduction. The puerperant women eligible for inclusion in the sampling were assigned to the experimental and control groups by randomization.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: intervention group
mobile app-based breastfeeding education
The main screen of the application used to be six screens. These six screens; Breastfeeding, Expressing, Contingencies, Frequently asked questions and my Breastfeeding Log and Breastfeeding diary. Mothers could record the number and duration of breastfeeding, milking status, the baby's height and weight, if it was a measure, the breastfeeding problem and solutions they encountered, on the "Breastfeeding Introduction" tab, and they could follow their breastfeeding status in the "Breastfeeding Diary" tab.
No Intervention: control group
rutin health care

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
breastmilk exclusive
Time Frame: postpartum 1st day- postpartum 8th week
rate of exclusive breastfeeding for eight weeks
postpartum 1st day- postpartum 8th week
breastfeeding problem
Time Frame: postpartum 1st day- postpartum 8th week
rate of breastfeeding problem eight weeks
postpartum 1st day- postpartum 8th week
baby's physical development
Time Frame: postpartum 1st day- postpartum 8th week
development of baby's weight, height and head circumference
postpartum 1st day- postpartum 8th week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

August 1, 2022

Study Completion (Anticipated)

August 1, 2022

Study Registration Dates

First Submitted

August 9, 2022

First Submitted That Met QC Criteria

August 9, 2022

First Posted (Actual)

August 11, 2022

Study Record Updates

Last Update Posted (Actual)

August 11, 2022

Last Update Submitted That Met QC Criteria

August 9, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 121S326

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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