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Construction and Preliminary Application of a Family Participatory Nursing Care Program for Breastfeeding of Maternal-Infant Separated Parturients Based on the Online-Offline Collaboration Model

Construction and Preliminary Application of a Family Participatory Nursing Care Program for Breastfeeding of Maternal-Infant Separated Parturients Based on the Online-Offline Collaboration Model

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102109
Enrollment
Unknown
Registered
2025-05-08
Start date
2025-03-15
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Maternal-Infant Separated Parturients

Interventions

control group:The control group received conventional treatment, nursing care, and breastfeeding education.
experimental group:The experimental group was provided with family-participatory nursing care based on the O2O model.

Sponsors

Xiamen Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Parturients: 1. Parturients who experience maternal-infant separation within 24 hours after childbirth; 2. Those aged 18 years or above; 3. Parturients with relatively stable conditions, clear consciousness, intact language expression and communication abilities; 4. Those who are able to fill out the questionnaire independently; 5. Mothers whose separation from their infants lasts for 3 days or more. Family members: 1. Those who are relatives of the patient (such as spouses, mothers, mothers-in-law, sisters, etc.) and live with the parturient (the care duration is more than 42 days); 2. Those aged 18 years or above; 3. Those who are aware of the parturient's disease diagnosis, condition and treatment; 4. Those who can use a smartphone, and have complete language expression ability and comprehension; 5.Those who voluntarily participate in this study under the principle of informed consent.

Exclusion criteria

Exclusion criteria: 1. Those with medical indications that prevent breastfeeding, such as being HIV-positive, syphilis-positive, in the active stage of pulmonary tuberculosis, etc.; 2. Those who do not plan to breastfeed due to a history of breast surgery, breast diseases, severe inverted nipples, etc.; 3. Those in critical condition (such as accompanied by severe postpartum hemorrhage, etc.) who have difficulty in cooperating with the research; 4.Parturients who used drugs that affect lactation (such as special antibiotics, sedatives, diuretics) during pregnancy or the puerperium due to treatment needs.

Design outcomes

Primary

MeasureTime frame
lactation volume;The success rate of breastfeeding;Questionnaire on Family Support for Breastfeeding;Self-efficacy in breastfeeding;

Secondary

MeasureTime frame
The level of breastfeeding knowledge;The mental health status of mothers;

Countries

China

Contacts

Public ContactLiu Fangfang

Xiamen Maternal and Child Health Care Hospital

371650718@qq.com+86 180 5004 1723

Outcome results

None listed

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