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A Family Centered Intervention Study on Breastfeeding Support for Premature Infants

A Family Centered Intervention Plan and Application Study on Breastfeeding Support for Premature Infants Based on Timing It Right

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070935
Enrollment
Unknown
Registered
2023-04-26
Start date
2023-05-01
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Certain conditions originating from the perinatal period (neonatal diseases related to short gestational weeks or low birth weight)

Interventions

intervention group:(1) Breastfeeding knowledge and skills support: Through online family meetings, explain the knowledge and skills of breastfeeding to premature mothers and their families, including
(2) Emotional support: By holding offline personalized psychological meetings to guide premature mothers and their families on how to alleviate negative emotions, guiding them to use breastfeeding dia
(3) Information support: Personalized WeChat groups are used to push breastfeeding behavior support tips to mothers and family members of premature infants. Follow up on breastfeeding status through W
control group:According to the routine nursing process, parents and primary caregivers of premature infants receive routine health education at the bedside on the day of admission, including the benef

Sponsors

Nursing College of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Premature infants: (1) 28w = birth gestational age<37w; (2) Transferred to NICU within 1 hour after birth; (3) Apgar score = 8 points (1 minute of birth). 2: Premature mother: (1) Age = 18 years old; (2) Primiparous women; (3) Willing to breastfeed; (4) At least one primary caregiver after childbirth, excluding fathers of premature infants; (5) No mental or cognitive impairment; (6) Informed consent, voluntary participation in this study, and signing of an informed consent form. 3: Fathers of premature infants: (1) Age = 18 years old; (2) No mental or cognitive impairment; (3) Willing to participate in this study and sign an informed consent form. 4: The main caregivers during the perinatal period are: (1) all = 18 years old; (2) For mothers of premature infants with a cumulative daily care time of no less than 3 hours, if the number of perinatal caregivers is = 2, the person with the largest total care time will be selected to enter this study; (3) No mental or cognitive impairment; (4) Willing to participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1: Premature infants: (1) suffer from congenital genetic metabolic diseases, congenital heart disease, developmental abnormalities; (2) Premature infants expected to be discharged within 1 week; (3) Premature infants cannot receive breastfeeding due to diseases or other reasons. 2: Mothers of premature infants: (1) mothers with special diseases should not breastfeed, such as AIDS, syphilis, serious heart disease, active tuberculosis, hepatitis, etc; (2) Participating in relevant intervention research projects that may change the observed outcomes; (3) Premature mothers have severe obstetric complications or complications, as well as other major diseases caused by non obstetric factors. 3: Premature father: participating in relevant intervention research projects that may change the observed outcomes. 4: The main caregivers during the perinatal period are: (1) participating in relevant intervention research projects that may change the observed outcomes; (2) Received training on breastfeeding knowledge and skills, such as the primary caregivers during the perinatal period being mothers in law or breastfeeding professionals.

Design outcomes

Primary

MeasureTime frame
Self efficacy of breastfeeding;Breastfeeding rate;Breastfeeding knowledge ;Breastfeeding skill ;

Secondary

MeasureTime frame
Premature infant height and weight;Postpartum depression ;Perceived social support;Breastfeeding Family Support;Father support breastfeeding self efficacy ;

Countries

China

Contacts

Public ContactGuo shengbin

Nursing Department of Fujian Maternal and Child Health Hospital

424408913@qq.com+86 13774518539

Outcome results

None listed

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