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Application of Prenatal Hand Milking Colostrum Collection in Promoting Lactation Initiation and Establishment

Application of prenatal hand milking in promoting lactation establishment

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089118
Enrollment
Unknown
Registered
2024-09-02
Start date
2023-07-17
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Lactation initiation and breastfeeding

Interventions

Intervention Group:Prenatal hand milking colostrum collection guidance
control group:Regular prenatal care education

Sponsors

Obstetrics and Gynecology Center of the Third Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 34 Years

Inclusion criteria

Inclusion criteria: Age 20-34 years old; Primiparous women; Pregnancy at 37 weeks; Natural conception; Single fetal head position; No severe pregnancy complications and/or complications; Willing to breastfeed; Healthy pregnant women who intend to give birth in our hospital; Accessible communication and communication; Volunteer to participate in this study.

Exclusion criteria

Exclusion criteria: Menopausal women; Non natural conception; Flat or inverted nipples in pregnant women; Have a history of breast surgery; Severe pregnancy complications and/or complications; Fetal growth restriction; Communication barriers or certain mental illnesses.

Design outcomes

Primary

MeasureTime frame
Lactation start time;Lactation establishment time;

Secondary

MeasureTime frame
Pure breastfeeding rate;Breastfeeding Self-efficacy Scale Short Form;The incidence of breast related symptoms during lactation;Delivery gestational age;Delivery method;Admission rate of neonatal jaundice NICU;

Countries

China

Contacts

Public ContactMingfang Zhou

Chongqing Medical University Affiliated Third Hospital

840464797@qq.com+86 187 0236 6551

Outcome results

None listed

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