Factors Affecting Postnatal Mother-To-Infant Bonding

November 24, 2025 updated by: Zehra Kan Onturk, Acibadem University

Factors Affecting Postnatal Mother-To-Infant Bonding: A Modelling Study

The aim of this study is to determine the factors that affect the postnatal mother-to-infant bonding.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Bonding is recognised as one of the fundamental processes in terms of the socio-emotional development of the infants and the relationship they establish with the outside world.Mother-to-infant bonding typically initiates during pregnancy and continues to evolve through early childhood, reflecting the mother's emotional orientation toward her infant. The initial postnatal period is the most favourable time for the initiation of a positive mother-to-infant relationship and bonding.An adequate mother-to-infant bonding contributes to the positive physical and socio-emotional development of the child. A weaker mother-to-infant bonding is associated with insecure attachment and depression and anxiety in children. Also, women with weaker mother-to-infant bonding have been found to show less interest in the health of their children. These behaviours cause long-term negative cognitive and socio-emotional development in the child.In a study that assessed the level of mother-to-infant bonding in the postnatal period and the associated factors, in general, a significant proportion of mothers had difficulties in mother-to-infant bonding in the postnatal period. The postpartum period is a critical, complicated period of transition for both the mother and the infant, considering psychological, social, and physiological difficulties. Therefore, the mother-to-infant bonding can be affected by many factors. The aim of this study is to determine the factors that affect the postnatal mother-to-infant bonding.

Study Type

Observational

Enrollment (Actual)

104

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

    • Ataşehir
      • Istanbul, Ataşehir, Turkey (Türkiye), 34750
        • Acıbadem University

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Mothers who give birth at the Maternity and Children's Hospital and their infants

Description

Inclusion Criteria:

  • All healthy mothers who applied to the hospital's maternity ward at the time of the study
  • who had a normal spontaneous delivery
  • infants who were born at ≥38 gestational weeks
  • infants who were deemed healthy by the physician were included in the study.

Exclusion Criteria:

  • Mothers who had a risky health problem during delivery
  • Infants who had a congenital illness

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Term newborn-mother group
The group consists of mothers who gave birth at the hospital where the study was conducted during the data collection period and were found to be eligible to participate in the study, along with their infants. No intervention was performed on the mothers or infants.
No intervention was performed on the mothers or infants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MIBS level
Time Frame: Immediately after completion of the first breastfeeding
After the first breastfeeding experience was completed, the mother assessed based on the mothers' self-reports using the Mother-Infant Bonding Scale (MIBS). The "MIBS", developed by Taylor et al., was used to assess mother-to-infant bonding following the first breastfeeding. The MIBS consists of 8 items rated on a 4-point Likert scale (0-3). Items 1, 4, and 6 assess positive emotions (scored as 0, 1, 2, 3), while items 2, 3, 5, 7, and 8 assess negative emotions (scored as 3, 2, 1, 0). Total scores range from 0 to 24, with lower scores indicating stronger mother-infant bonding. The tool has no specific cut-off value and has been shown to be sensitive in detecting subtle variations in early maternal bonding.
Immediately after completion of the first breastfeeding

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Merve Coşkun, Assist.Prof., Acibadem University

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)

August 1, 2019

Primary Completion (Actual)

May 1, 2022

Study Completion (Actual)

May 1, 2022

Study Registration Dates

First Submitted

November 18, 2025

First Submitted That Met QC Criteria

November 24, 2025

First Posted (Actual)

November 26, 2025

Study Record Updates

Last Update Posted (Actual)

November 26, 2025

Last Update Submitted That Met QC Criteria

November 24, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 62/2019

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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