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Laid Back Breastfeeding Position on Breastfeeding Experience

NCT07196202 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2025-09-29

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the effect of laid back breast feeding position on breastfeeding experience among multiparous women. The main questions it aims to answer are;

* Do postpartum women who feed their babies in a laid-back position report a better breastfeeding experience than those who use the cradle position?
* Do postpartum women who feed their babies in a laid-back position report greater breastfeeding comfort than those who use the cradle position? Researchers will compare breastfeeding in laid-back position to cradle position to see if postpartum women who feed their babies in a laid-back position have better breastfeeding experience and comfort

Participants will:

* Have educational sessions on breastfeeding in laid-back position during antenatal visit of the 3rd trimester
* Will be followed by the researcher for any clarifications about the educational content of session
* Will be asked to apply laid-back position after giving birth, so, the researcher evaluate its effect on breastfeeding experience and comfort.

Conditions

  • Maternal Breastfeeding Experience
  • Maternal Breastfeeding Comfort

Interventions

OTHER

Standard Postpartum Care

Postpartum mothers who receive structured training and support on the laid-back breastfeeding position

OTHER

Laid-Back position training

This intervention is a structured training session for pregnant woman on the use of the laid-back breastfeeding position after birth. The training is designed to be delivered in a single, standardized session by the researcher during the last trimester of pregnancy to be applied within the first 24 hours post-cesarean delivery.

Sponsors & Collaborators

  • Mansoura University

    lead OTHER

Principal Investigators

  • Nadia Y AbdElla, Asistatnt Professor · Faculty of Nursing- Mansoura University- Egypt

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2026-08-01
Completion
2026-12-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07196202 on ClinicalTrials.gov