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The Effect of Breast Crawl Intervention on Postpartum Lactation and Maternal Emotional Experience in Vaginal Deliveries

The Effect of Breast Crawl Intervention on Postpartum Lactation and Maternal Emotional Experience in Vaginal Deliveries

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099756
Enrollment
Unknown
Registered
2025-03-28
Start date
2022-12-05
Completion date
Unknown
Last updated
2025-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding

Interventions

breast crawl group:The study group received the breast crawl intervention.
Control group:The control group received conventional skin-to-skin contact

Sponsors

Women and Children’s Hospital, School of Medicine, Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Maternal Criteria: Women who underwent vaginal delivery. Aged over 18 years. Normal breast development without anatomical or functional abnormalities. Capable of effective communication, comprehension, and completion of the study questionnaire. Provided informed consent for participation. 2. Neonatal Criteria: Full-term infants with a gestational age of 37–42 weeks. Apgar score of >= 8 at 1 minute after birth. Birth weight ranging from 2500 to 4000 g.

Exclusion criteria

Exclusion criteria: Exclusion criteria included maternal or neonatal conditions unsuitable for breast crawl and breastfeeding, such as acute infectious diseases, acute bacterial or viral infections, and undergoing radioactive iodine therapy.

Design outcomes

Primary

MeasureTime frame
Rate of Exclusive Breastfeeding;Anxiety lever;breastfeeding knowledge ;breastfeeding attitudes;

Secondary

MeasureTime frame
Rate of Successful Initiation of Breastfeeding;the time of lactation initiation;

Countries

China

Contacts

Public ContactHuang Lingling

Women and Children’s Hospital, School of Medicine, Xiamen University

51862961@qq.com+86 159 8588 8705

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026