NCT07149766

Brief Summary

Breast crawling, also referred to as the newborn's self-attachment, was first observed in 1977 and described as the "first important sucking behavior". During the first hour after birth, the newborn exhibits instinctive movements aimed at locating and attaching to the breast. In 1987, Swedish researchers Widström et al., and later in 1990, Righard and Alade, detailed these behaviors through systematic observation. They found that when a newborn is placed prone on the mother's abdomen immediately after birth-while the mother is in a supine position-the baby begins to engage rooting and stepping reflexes. These reflexes typically lead the baby to begin crawling toward the breast around 29 minutes after birth, with effective suckling starting approximately 50 minutes postpartum.This instinctual behavior, observed in the first hour of life when the newborn is most alert and active, has been well documented in the literature as "the breast crawl." It demonstrates the neonate's innate capacity to find and latch onto the mother's breast using biological reflexes when uninterrupted. Righard and Alade emphasized that routine hospital practices often interrupt this natural sequence, which may negatively impact the breastfeeding process. They underlined the importance of preserving the immediate postnatal hour, a critical window in which these behaviors are most likely to occur and support early breastfeeding success.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 18, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

August 25, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 2, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2025

Completed
Last Updated

January 2, 2026

Status Verified

December 1, 2025

Enrollment Period

3 months

First QC Date

July 18, 2025

Last Update Submit

December 28, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Postpartum Comfort Scale

    Description: Measures physical, psychological, and environmental comfort after childbirth. (The scale is a 34-item Likert-type scale. The lowest possible score is 34, and the highest is 170. A higher score indicates higher postpartum comfort.)

    Within the first 24 hours postpartum

  • Postpartum Breastfeeding Self-Efficacy Scale

    Description: Evaluates the mother's confidence in her ability to breastfeed successfully. The minimum score that can be obtained from the scale is 14, and the maximum score is 70. The scale has no cut-off point, and a higher score indicates higher breastfeeding self-efficacy.

    At 24 hours postpartum

Secondary Outcomes (1)

  • Demographic Information Form

    baseline

Study Arms (2)

intervention group

EXPERIMENTAL
Other: Breast crawling

Control group

NO INTERVENTION

Interventions

The newborn will be placed on the mother's abdomen for no more than 60 minutes, during which breast crawling and suckling behaviors will be observed. Throughout this period, the researcher will maintain active communication with the mother, providing information on the importance of breastfeeding. The mother will be gently guided to support the baby when necessary, without interfering with the baby's natural instincts. The newborn's heart rate, respiratory rate, and body temperature will be recorded at birth and at the 60th minute.

intervention group

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnacy
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Being over 18 years of age,
  • Volunteering to participate in the study,
  • Ability to speak, write, and understand Turkish,
  • No communication difficulties,
  • Having had a spontaneous vaginal delivery,
  • Primigravida giving birth for the first time,
  • The baby was given to the mother within the first hour after birth,
  • Having a full-term, singleton, and healthy newborn,
  • No condition preventing breastfeeding in either mother or baby.
  • The baby was born with an APGAR score of 7 or higher,
  • The baby had no tongue, lip, or mouth anomalies,
  • Coordination of sucking, rooting, and swallowing was present.

You may not qualify if:

  • The mother did not want to participate in the study or wished to terminate the study,
  • The mother had a postpartum emergency requiring medical intervention.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sakarya University

Sakarya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Breast Feeding

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 18, 2025

First Posted

September 2, 2025

Study Start

August 25, 2025

Primary Completion

November 15, 2025

Study Completion

December 20, 2025

Last Updated

January 2, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

For ethical reasons, patient information may be shared upon reasonable request without revealing their identities for security reasons.

Locations