The Effect of Maternal Role Training Program on Maternal Role Attainment Mother Infant and Father Infant Attachment

August 10, 2024 updated by: Zeliha Karapelit, Amasya University

The Effect of Maternal Role Training Program Based on Theory on Maternal Role Attainment Mother Infant and Father Infant Attachment

Aim: This study was conducted to determine the effect of education prepared according to the Mother Role Attainment Theory on mothering role, mother-infant attachment,father-infant attachment Material and Method: The study was conducted with primiparous pregnant women and their spouses who applied to Amasya University Sabuncuoğlu Serefeddin Training and Research Hospital between June 2021 and May 2022 as a pretest-posttest quasi-trial model with a control group. The study was completed with 109 parents (54 experimental group, 55 control group). Introductory Information Form, Prenatal Attachment Scale, Semantic Difference Scale (Me as Mother - My Baby), Maternal Attachment Scale, Pharis Self-Confidence Scale, Prenatal Father Attachment Scale and Father-Baby Attachment Scale were used to collect data. Institutional and ethical permissions were obtained to start the research. As a nursing approach, a 4-session motherhood identity development training was given to the experimental group based on the Maternal Role Attainment Theory.Number, percentage, mean, standard deviation, chi-square dependent and independent groups t test, Mann Whitney U test and Wilcoxon sign test were used in the analysis of the data.

Study Overview

Status

Completed

Detailed Description

After the pre-test was applied to the mother and father candidates included in the experimental group, "Maternity Identity Development Training" was given in the prenatal and postnatal period. This training program, based on Ramona T. Mercer's model of mothering role ability and covering four stages, was given to parents in their own homes by taking the necessary precautions, since it would be risky for the participants to be given in groups due to the COVID-19 Pandemic process. The training, which consisted of 2 sessions in the last trimester of pregnancy, 2 sessions at the end of the delivery before discharge and within the first week, and 4 sessions in total, lasted approximately 40 minutes. In addition, the parents in the training group were given a training booklet and the researcher's phone number for counseling and follow-up if needed.The training booklet, which contains the same information as the training content, was given to the parents in the experimental group at the end of the first training, and to the parents in the control group after the post-tests were administered.

Study Type

Interventional

Enrollment (Actual)

109

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

      • Amasya, Turkey, 05100
        • Amasya Universty

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • At least primary school graduate
  • Being at 28-32 weeks of gestation
  • Age range of 18-45
  • Married and living with her spouse
  • Living in the center of Amasya
  • Willingness to communication and cooperation
  • There is no risk in terms of maternal and fetal health.
  • Not having a psychiatric health problem

Exclusion Criteria:

  • Those outside the determined gestational week
  • Those who are closed to communication and cooperation
  • People living outside the city center of Amasya
  • Those with health problems or risky pregnancies were not included in the study. Exclusion Criteria
  • Loss of fetus
  • Not participating/completing the trainings for any reason
  • Change of residence outside the province
  • Giving birth in another hospital
  • Having maternal and/or newborn health problems
  • To fill in the assessment tests incompletely/not at all

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: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: experimental group
As a nursing approach, a 4-session motherhood identity development training was given to the experimental group based on the Maternal Role Attainment Theory
Monitoring the Effect of the Education Given to Parents According to Maternal Role Ability Theory on Maternal Role Mother-Baby and Father-Infant Attachment
No Intervention: control group
Not intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prenatal Father Attachment Scale
Time Frame: third trimester of pregnancy, before training

The minimum score that can be obtained from the scale is 16, while the maximum score is 80.

As the score obtained from the scale increases, the level of attachment also increases.

third trimester of pregnancy, before training
Prenatal Attachment Inventory
Time Frame: third trimester of pregnancy, before training

From the scale, where the level of attachment increases as the score increases, the lowest score can be 21 and the highest score can be 84.

As the score obtained from the scale increases, the level of attachment also increases.

third trimester of pregnancy, before training
Father-Baby Attachment Scale
Time Frame: 42nd day postpartum

High scores indicate high levels of attachment.A high mean score is evaluated positively.Each item of the scale is scored from 1 to 5 and The lowest score that can be obtained from the scale is 19 and the highest score is 95.

is changing

42nd day postpartum
Maternal Attachment Scale
Time Frame: 42nd day postpartum
It is stated that as the score obtained from the scale increases, the level of attachment also increases.A high score indicates high maternal attachment. The lowest score obtained from the scale varies between 26 and the highest score 104.
42nd day postpartum
Semantic Differential Scale-Me as a Mother
Time Frame: third trimester of pregnancy, before training and 42nd day postpartum
The lowest score from the scale is 11, the highest score is 77, and high scores indicate positive motherhood self-evaluation.
third trimester of pregnancy, before training and 42nd day postpartum
Semantic Differential Scale-My Baby:
Time Frame: third trimester of pregnancy, before training and 42nd day postpartum
The lowest score from the "My Baby" scale is 6, the highest score is 42, and high total scores indicate the evaluation of positive baby perception.
third trimester of pregnancy, before training and 42nd day postpartum
Pharis Self-Confidence Scale
Time Frame: third trimester of pregnancy, before training and 42nd day postpartum
The lowest score from the "Pharis Self-Confidence" scale is 1 and the highest score is 65, and high total score results indicate high self-confidence in baby care.
third trimester of pregnancy, before training and 42nd day postpartum

Collaborators and Investigators

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

Investigators

  • Study Director: Behice Erci, professor, Inonu University

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)

June 15, 2021

Primary Completion (Actual)

December 15, 2021

Study Completion (Actual)

May 10, 2022

Study Registration Dates

First Submitted

September 5, 2023

First Submitted That Met QC Criteria

August 10, 2024

First Posted (Actual)

August 14, 2024

Study Record Updates

Last Update Posted (Actual)

August 14, 2024

Last Update Submitted That Met QC Criteria

August 10, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

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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