Breastfeeding Support Provided to Mothers Through WhatsApp Messaging Application

November 26, 2021 updated by: Sevda KORKUT ÖKSÜZ, Ahi Evran University Education and Research Hospital

The Effect of Continuous Breastfeeding Support Provided to Mothers Through WhatsApp Messaging Application on Breastfeeding: A Randomized Controlled Trial

The research was planned as a randomized controlled experimental study in order to determine the effect of continuous breastfeeding support provided to mothers through WhatsApp messaging application on breastfeeding.

Research Hypotheses H0: Continuous breastfeeding support provided to mothers through WhatsApp messaging application has no effect on breastfeeding.

H1: Continuous breastfeeding support provided to mothers through WhatsApp messaging application increases the rate of exclusive breastfeeding.

H2: Continuous breastfeeding support provided to mothers through WhatsApp messaging application increases the breastfeeding duration of the mothers.

H3: Continuous breastfeeding support provided to mothers through WhatsApp messaging application reduces the rate of mothers giving their babies other foods than breast milk.

H4: Continuous breastfeeding support provided to mothers through WhatsApp messaging application reduces bottle feeding rates.

H5: Continuous breastfeeding support provided to mothers through WhatsApp messaging application reduces the rate of pacifier use.

H6: Continuous breastfeeding support provided to mothers through WhatsApp messaging application reduces the incidence of mothers' breastfeeding problems.

H7: Continuous breastfeeding support provided to mothers through WhatsApp messaging application affects mothers' breastfeeding attitude positively.

H8: Continuous breastfeeding support provided to mothers through WhatsApp messaging application increases the motivation of breastfeeding mothers.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

METHOD:

Place of the Research:

The data of the research will be collected in the postpartum service of Zeynep Kamil Women And Chıldren Dıseases Tranıng And Research Hospıtal in Istanbul. After then 6 months of follow-up will be continued trough WhatsApp application.

The Universe and the Sample of the Research:

The universe of the research; It will comprise primipa mothers and babies who are hospitalized in the postpartum ward of the specified dates, deliver vaginal or cesarean delivery, and meet the sample selection criteria.

The sample of the research was determined by statistic analysis by power analysis. Power analysis was performed by using G * Power (v3.1.7) program to determine the number of samples. The power of the study is expressed as 1-β (olasılığı = type II error probability) and research should generally have 80% power. According to Cohen's effect size coefficients; Assuming that the evaluations to be made between the two independent groups will have a medium effect size (d = 0.5), considering the fact that there should be at least 64 people in the groups and there may be losses in the working process, each group decided to recruit 70 people. 140 people in total. it is given. Computerized randomization method will be used in the research.

In the collection of research data; Mother and Newborn Data Collection Form Postpartum Breastfeeding Evaluation and Follow-up Form Application Satisfaction Evaluation Form Breastfeeding Attitudes of The Evaluation Scale Primipara Breastfeeding Motivation Scale (PBMS) 5 data collection forms will be used.

Application of the research:

The researcher will briefly talk about the scope and content of the research by meeting with the mothers who meet the case selection criteria. Written consents will be obtained through the "Informed Volunteer Consent Form" asking mothers whether they want to participate in the study. Mothers who wish to participate in the study will be randomly determined by computer-assisted randomization method. Applications made after randomization will be carried out with the following steps; Experimental group; Information will be obtained from the mothers who agreed to participate in the study in line with the "Mother and Newborn Data Total Form", Mothers participating in the study will receive routine breastfeeding training at the hospital after birth, The breastfeeding attitude of the mother will be evaluated with the "Breastfeeding Attitude Scale", and the breastfeeding motivation of the mother will be evaluated with the "Breastfeeding Motivation Scale", In line with the needs of the mothers, breastfeeding support and motivation will be provided, In the first 1 month, basic standard information sharing (see "Basic Standard Information Sharing") will be made determined by the researcher. Later, information sharing will be made regarding the questions and problems of the mother, Individual breastfeeding support provided to mothers through WhatsApp will continue for 6 months, Mothers will be contacted once a week through WhatsApp and feedback will be received on the breastfeeding process, The questions of the mother regarding breastfeeding will be answered by text / voice message or video call, In the postpartum period (day 7, day 15, month 1, month 2, month 4 and month 6) mothers will be called by phone. Breastfeeding conditions will be evaluated with "Postpartum Breastfeeding Evaluation and Follow-up Form".

Breastfeeding attitudes of the mothers will be assessed with the Breastfeeding Attitudes of the Evaluation Scale" before breastfeeding education in hospital and through online survey at the 6th Month.

Breastfeeding motivations of the mothers will be assessed with the " Primipara Breastfeeding Motivation Scale " through online survey at the 6th Month.

The mothers' satisfaction with the continuous breastfeeding support provided through WhatsApp will be evaluated with the "Application Satisfaction Evaluation Form" through online survey.

Basic Standard Information Sharing; New coronavirus (COVID-19) and breastfeeding Suggestion on breastfeeding (motivational-enhancing videos that emphasize breastfeeding is instinctive) The importance of breast milk (positive effects on mother and baby will be explained) Sharing of health institutions emphasizing the importance of breastfeeding (WHO, UNICEF, Ministry of Health) Milk production of breasts (Frequent breastfeeding will be supported by videos) Baby holding the breast (Mothers will be emphasized that the baby's sucking ability instinctively and will be supported with videos) Skin-to-skin contact and breastfeeding Reasons for breastfeeding only for the first 6 months Symptoms that show that the baby is sucking effectively Control Group; Information will be obtained from the mothers who agreed to participate in the study in line with the "Mother and Newborn Data Total Form", Mothers participating in the study will receive routine breastfeeding training at the hospital after birth, The breastfeeding attitude of the mother will be evaluated with the "Breastfeeding Attitude Scale", and the breastfeeding motivation of the mother will be evaluated with the "Breastfeeding Motivation Scale", In line with the needs of the mothers, breastfeeding support and motivation will be provided, In the postpartum period (day 7, day 15, month 1, month 2, month 4 and month 6) mothers will be called by phone. Breastfeeding conditions will be evaluated with "Postpartum Breastfeeding Evaluation and Follow-up Form".

Breastfeeding attitudes of the mothers will be assessed with the Breastfeeding Attitudes of the Evaluation Scale" before breastfeeding education in hospital and through online survey at the 6th Month.

Breastfeeding motivations of the mothers will be assessed with the " Primipara Breastfeeding Motivation Scale " through online survey at the 6th Month.

Analysis:

NCSS (Number Cruncher Statistical System) 2007 (Kaysville, Utah, USA) program will be used for statistical analysis of the research. Statistical significance will be accepted as p <0.05.

Study Type

Interventional

Enrollment (Actual)

150

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

  • Turkey
    • Üsküdar
      • İstanbul, Üsküdar, Turkey, 34660
        • Zeynep Kamil Women And Chıldren Dıseases Tranıng And Research Hospıtal

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 to 49 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

For the mother;

  • 18 years and older
  • Primipar,
  • Having healthy pregnancy and uncomplicated birth,
  • No health problems preventing breastfeeding (drug use, HIV, etc.),
  • Not having any obstacle to communication (not knowing Turkish, mental retardation etc.),
  • Being literate,
  • Having a smart phone and internet connection,
  • It was determined to be able to use WhatsApp application. For baby;
  • Being healthy and term
  • No health problems preventing breastfeeding (Esophageal atresia, cleft palate, cleft lip etc.)
  • Its weight is between 2500-4000 gr.
  • It was determined that the Apgar Score was above 7.

Exclusion Criteria:

  • Mothers with multiple pregnancies,
  • Infants lying in NICU due to health problems in the postpartum period will be excluded from the scope of the research.

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: WhatsApp Messaging Application
Continuous breastfeeding support will be provided for the first 6 months through WhatsApp messaging application. Mothers will be contacted once a week through WhatsApp and feedback will be received on the breastfeeding process. The questions of the mother regarding breastfeeding will be answered by text / voice message or video call.
Other: Breastfeeding Support Provided to Mothers Through WhatsApp Messaging Application
Breastfeeding support provided to mothers through WhatsApp messaging application will be maintained for the first 6 months after birth. In the first 1 month, standard information sharing will be made through whatsApp. Also, for the first 6 months, solutions generating shares will be made according to the problems and questions of the mother regarding breastfeeding.
No Intervention: Standard breastfeeding support
She will receive standard breastfeeding support after delivery. Breastfeeding will not receive continuous breastfeeding support for the first 6 months after discharge.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Breastfeeding Attitudes of The Evaluation Scale
Time Frame: In our study, will be applied before breastfeeding education in hospital and through online survey at postpartum 6th months for both groups

This scale assesses various aspects of attitudes that direct mothers' breastfeeding behavior. Examines breastfeeding as behavior.

The scale is a five-point Likert type consisting of 46 items, easy to apply, and which people can answer on their own, and it can be applied to all mothers. Some items in the scale (3, 4, 6, 7, 8, 11, 13, 15, 19, 23, 24, 26, 27, 28, 29, 30, 31, 32, 37, 38, 42, 43) As a positive attitude, I agree with the statement "I totally disagree" to 4-3-2-1-0, while some items (1, 2, 5, 9, 10, 12, 14, 16, 17, 18, 20, 21 (22, 25, 33, 34, 35, 36, 39, 40, 41, 44, 45, 46) are considered negative, and the opposite score is scored as 0-1-2-3-4 from the statement entirely agree. In this way, the total score that can be obtained from the scale is between 0 and 184. As the score increases, breastfeeding attitude is evaluated as positive.
In our study, will be applied before breastfeeding education in hospital and through online survey at postpartum 6th months for both groups
Primipara Breastfeeding Motivation Scale (PBMS)
Time Frame: at postpartum 6th months through online survey for both groups

This scale evaluates postpartum breastfeeding motivation level in primiparous. The scale consists of 24 items in total. After applying to the sample group, the factor analysis of the scale was made and it was determined to have 5 factors.

  1. Intrinsic motivation and integrated regulation
  2. Identified regulation

  3. Mirrored editing

    External regulation is examined in two sub-dimensions:

  4. External regulation (instrumental needs)
  5. External regulation (baby health) Scale items are rated from 1 = Never disagree to 4 = Strongly agree. The scale is in 4-point Likert type, and each item is scored between 1-4. The scale does not have a total score. The score of the sub-dimensions is calculated by taking the average of the scale sub-dimension scores. As the score obtained from the sub-dimension of the scale increases, the motivation representing that sub-dimension increases.
at postpartum 6th months through online survey for both groups
Application Satisfaction Evaluation Form
Time Frame: at postpartum 6th months through online survey for only experimental group

Evaluates the satisfaction of mothers from breastfeeding support provided through WhatsApp messaging application.

It is a form consisting of 10 questions by the researcher to evaluate the satisfaction of the mothers from the breastfeeding support given through the social media group (WhatsApp) by making use of the literature information.

The answer to each question will be evaluated as yes / no. In the tenth question, he will be asked to score the application. There will be a minimum of 1 and a maximum of 10 points.
at postpartum 6th months through online survey for only experimental group

Collaborators and Investigators

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

Sponsor

Ahi Evran University Education and Research Hospital

Investigators

  • Principal Investigator: Sevda KORKUT ÖKSÜZ, R.A, Kirsehir Ahi Evran Universitesi

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.

General Publications

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)

December 1, 2020

Primary Completion (Actual)

February 28, 2021

Study Completion (Actual)

September 1, 2021

Study Registration Dates

First Submitted

July 16, 2020

First Submitted That Met QC Criteria

July 16, 2020

First Posted (Actual)

July 21, 2020

Study Record Updates

Last Update Posted (Actual)

November 29, 2021

Last Update Submitted That Met QC Criteria

November 26, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • AhiEvranU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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