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Maternal Breastfeeding ExperienceLBB/PBENCT07196202

Laid Back Breastfeeding Position on Breastfeeding Experience

A study testing Laid-Back position training and Standard Postpartum Care in people with Maternal Breastfeeding Experience and Maternal Breastfeeding Comfort, run by Mansoura University at 2 sites in Egypt.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial 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… Read more about this study

Who is it for?
Ages 20 to 35 years, women onlyHealthy volunteers can take part
What is being tested?
Laid-Back position training and Standard Postpartum Care
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
168 participants
Where
2 sitesEgypt
Study dates
1 Dec 2025to 1 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 35 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Multiparous women aged 20 -35 years.
  • Multiparous women At the 34 to 36 weeks of gestational age
  • Multiparous women with normal course of pregnancy with single-tone fetus
  • Multiparous women planning to deliver at Mansoura University Hospital
  • Multiparous women who will perform elective caesarian section
  • Multiparous women planning to breast feed their babies
Show all 9Show fewer
  • Multiparous women who have no information about laid breastfeeding position
  • Multiparous women who will deliver neonate with normal ABGAR score
  • Multiparous women who will deliver neonate weight 2.5: 3.5 kg.

Who cannot join

  • Mothers who had inverted or flat nipple.
  • Mothers who have postpartum complications
  • Mothers who delivered babies with cleft lip, cleft palate, preterm, neurological deficit, asphyxia or any abnormal condition will be excluded from the study.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Nadia Y AbdElla, Assisttant professor contact

+20-50-2733200

drnadiaabdella@gmail.com

Egypt2 sites
  • Mansoura University Hospitals

    Al Mansurah, Dakahlia Governorate, 35511

  • New Obstetric and Gynecological Center

    Al Mansurah, Dakahlia Governorate, 35511

Other trials in Egypt

About this study

Official title: Effect of Laid Back Breastfeeding Position on Breastfeeding Experience Among Multiparous Women

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
Read more

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.
Read the detailed description

Cesarean sections are major surgeries that can cause pain and complications, making early breastfeeding initiation less likely compared to vaginal birth. This is problematic because early breastfeeding has significant health benefits for both mother and infant. Breastfeeding outcomes after C-sections are often worse, including delays, more difficulties, and shorter duration.

A common cause of these problems is inadequate breastfeeding technique. The laid-back breastfeeding position is a simple method that relies on the mother's intuition and the baby's natural reflexes, requiring little professional guidance.

This study used a quasi-experimental research design. It will conducted at the antenatal outpatient clinic and inpatient wards of Mansoura University Hospital. The study involved a total of 168 participants. Pregnant mothers in intervention group will be trained to breastfeed their infants using the laid-back position.

Being tested
Laid-Back position training, Standard Postpartum Care
Keywords
laid back position, breastfeeding experience, breastfeeding comfort

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Laid-Back position trainingOther

    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.

  • Standard Postpartum CareOther

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

Study groups in NCT07196202
Study groupRoleWhat they receive
Laid-Back Positioning GroupActive comparatorMultiparous women who receive structured training and support on the laid-back breastfeeding position during the last trimester of pregnancy so, they can apply it after giving birth
Receives: Other: Laid-Back position training
Standard Care GroupPlacebo comparatorMultiparous women who receive the standard postpartum breastfeeding care and support offered by the hospital after giving birth
Receives: Other: Standard Postpartum Care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Breastfeeding Experience Scale (BES)

    BES consists of 30 items (18- items to assess presence or absence and severity of common breastfeeding difficulties in the early postpartum period and 12 items to assess breastfeeding continuation and the reasons for weaning). In the current study, the researcher used the 18 item part of BES because it suites the aim of the study. The 18-item part are divided into five categories including 3items for breast concern, 5 items for mechanics of breast concern, 5 items for process concern, 3 items for insufficient milk production and 2 items for social concern.

    Scoring system The score system for breastfeeding difficulties using three point Likert scale ranged from "never" (1), "sometimes" (2) and "always" (3). The total scores were ranged from 18 to 54. the level of difficulties were categorized as the following: low severity (< 60%) were ranged from 0 > 32point, average severity (60 % to < 80%) were ranged from 32 > 43 point and high severity (≥80 %) were ranged from 43≥ 54 point.

    Measured: 1st time for assessment will be within 24 to 48 hrs after giving birth. 2nd time for assessment will be one week after birth.

Secondary outcomes (1)
  1. Maternal comfort during breastfeeding (MCRS)

    MCRS consists of 9 items describes the maternal feelings during breastfeeding including maternal relaxation during feeding, degree of maternal confidence to hold her baby in laid back position during feeding....ect.

    Scoring system for MCRS The total scores Maternal comfort ranged from 9 to 36 then the level of comfort categorized as; low < 60% (9 - 21); moderate 60% to <75% (22 - 27) \& high ≥ 75% (28 - 36).

    Measured: One week after delivery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Sep 2025
  2. Study start1 Dec 2025 (estimated)
  3. Primary completion1 Aug 2026 (estimated)
  4. Study completion1 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
One group of mothers (the intervention group) will be trained on the laid-back position. The other group (the control group) will receive standard care. The outcomes for these two distinct groups were then compared. The groups will treated independently and in parallel.
Masking
None (open label)
Enrolment
168 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07196202
Sponsor's protocol ID
0669
Acronym
LBB/PBE
Status last verified
Sep 2025
First submitted
19 Sep 2025
Last updated
29 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The reason for not sharing data is to comply with and protect the confidentiality of participants, which is a primary ethical requirement in research.

Questions about this trial

What is this clinical trial studying?

A study testing Laid-Back position training and Standard Postpartum Care in people with Maternal Breastfeeding Experience and Maternal Breastfeeding Comfort, run by Mansoura University at 2 sites in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 29 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Nadia Y AbdElla, Assisttant professor (+20-50-2733200, drnadiaabdella@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Breastfeeding Experience Scale (BES) (time frame: 1st time for assessment will be within 24 to 48 hrs after giving birth. 2nd time for assessment will be one week after birth.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2025.

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