Breast Crawling and Breastfeeding Success
1 other identifier
interventional
80
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
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
CompletedStudy Start
First participant enrolled
August 25, 2025
CompletedFirst Posted
Study publicly available on registry
September 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 20, 2025
CompletedJanuary 2, 2026
December 1, 2025
3 months
July 18, 2025
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
EXPERIMENTALControl group
NO INTERVENTIONInterventions
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.
Eligibility Criteria
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)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
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.