The Effect of Breastfeeding Education Using a Doll During Pregnancy on Newborn Feeding

Sponsor
Istanbul University - Cerrahpasa (IUC) (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05853653
Collaborator
Istinye University (Other)
209
1
2
8
26.3

Study Details

Study Description

Brief Summary

This study was planned in a randomized controlled quasi-experimental design to determine the effect of breastfeeding education using a doll during pregnancy on newborn feeding. Necessary institutional and ethics committee permissions will be obtained before the study. Before data collection, the consent form will be read to the pregnant women who meet the inclusion criteria and volunteer to participate in the study and their written and verbal consent will be obtained. The information in the participant information form will be questioned before the training. In the prenatal period of the study, the Control group will be given the standard breastfeeding education applied by the institution verbally. In the intervention group, breastfeeding education prepared in line with the relevant literature will be given by the researchers. Individual breastfeeding training will be given to each participant by a researcher.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Using dolls in breastfeeding education
N/A

Detailed Description

The most important nutrient in infant nutrition has been breast milk throughout history. Breastfeeding has many benefits for both the infant, the mother and the society. In addition to reducing mortality and morbidity rates in infants, it provides a healthy growth and development process. It has positive effects on the mother such as feeling happy, being physically healthy with the effect of hormones, facilitating the return of the uterus, providing emotional satisfaction, reducing the risk of breast cancer, reducing the risk of anemia, reducing the risk of depression, facilitating mother-infant bonding, and protecting from a new pregnancy. In addition, being free and natural, decreasing maternal-infant mortality, decreasing the risk of disease, providing healthy individuals to the society, being fast and requiring preparation, decreasing health expenditures, decreasing the loss of labor force, decreasing the risk of loss of money for working mothers were the benefits to the society and the country. In the world and in our country, many practices are carried out to popularize breastfeeding. One of the most important of these practices is the friendly hospital practice, which informs pregnant women and families about the importance of breastfeeding. Skin-to-skin contact between mother and baby is ensured immediately after birth, and the mother is supported to start breastfeeding as soon as possible and not to interrupt contact (Bolat et al, 2011; Samur, 2006). This approach aims to increase the rate of breastfeeding. However, in the changing world order, there may be problems in maintaining the maternal herd due to the inclusion of women in business life. For this reason, practices to promote breastfeeding are on the agenda. The primary aim of these practices is to provide exclusive breastfeeding for the first 6 months, supplementary feeding from the 6th month onwards and continuation of breastfeeding until the age of 2 years. Within the scope of the "Promotion of Breastfeeding and Baby Friendly Hospitals Program" in our country, it is aimed to reach all hospitals where births are performed and to provide education and information in these hospitals. For this reason, prenatal and postnatal breastfeeding and breastfeeding education is provided by health professionals. It is also recommended that this education should be shaped according to the needs of women, the content should be diversified, teaching should be carried out by using technology, and continuity of education should be ensured.

Study Design

Study Type:
Interventional
Actual Enrollment :
209 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized controlled quasi-experimental designRandomized controlled quasi-experimental design
Masking:
Single (Participant)
Masking Description:
Single blind
Primary Purpose:
Supportive Care
Official Title:
The Effect of Breastfeeding Education Using a Doll During Pregnancy on Newborn Feeding: A Randomized Control Trial
Actual Study Start Date :
Oct 1, 2022
Actual Primary Completion Date :
Apr 15, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Using dolls in breastfeeding education

In the breastfeeding training, the researchers will explain the pre-created training content. It will then be demonstrated practically using the baby. A training brochure will be given at the end of the training.

Behavioral: Using dolls in breastfeeding education
Using dolls in breastfeeding education

No Intervention: Verbal expression is used in breastfeeding education

In the breastfeeding training, the researchers will verbally explain the pre-created training content. A training brochure will be given at the end of the training.

Outcome Measures

Primary Outcome Measures

  1. Effective use of dolls and breastfeeding education [6 months]

    The effect of breastfeeding education using dolls will be obtained by analyzing the data collected with data collection tools.

  2. Effect of breastfeeding education on breastfeeding self-efficacy level [6 months]

    The effect of breastfeeding education on the level of breastfeeding self-efficacy will be obtained by analyzing the data.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Being in the last trimester of pregnancy

  • Having a healthy pregnancy

  • Fetus and newborn are healthy

  • Having the mother and baby in the same room in the postpartum period

Exclusion Criteria:
  • Not knowing Turkish

  • The woman has neurological and cognitive problems

  • Hearing and vision problems in the woman

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aysegul Simsek Istanbul Zeytinburnu Turkey 34010

Sponsors and Collaborators

  • Istanbul University - Cerrahpasa (IUC)
  • Istinye University

Investigators

  • Principal Investigator: Aysegul Simsek, PhD, Istinye University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Aysegul Simsek, Assist. Prof. Dr., Istanbul University - Cerrahpasa (IUC)
ClinicalTrials.gov Identifier:
NCT05853653
Other Study ID Numbers:
  • IstinyeU
First Posted:
May 11, 2023
Last Update Posted:
May 11, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Aysegul Simsek, Assist. Prof. Dr., Istanbul University - Cerrahpasa (IUC)

Study Results

No Results Posted as of May 11, 2023