Skip to content

Developing a Sustained Implementation Plan for Evidence-Based Group Parenting and Health Care Practice Among Mothers of Preterm Infants: An Implementation Study

Developing a Sustained Implementation Plan for Evidence-Based Group Parenting and Health Care Practice Among Mothers of Preterm Infants: An Implementation Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127725
Enrollment
Unknown
Registered
2026-07-06
Start date
2026-07-06
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Preterm birth is defined as delivery occurring at >=28 and <37 gestational weeks. This study focuses on group-based parenting education for mothers of preterm infants, with the aim of improving maternal parenting efficacy.

Interventions

Control group:Routine postpartum health education
Intervention group:The intervention group will receive the Group Parenting and Health Care Practice Strategy Package for Mothers of Preterm Infants, developed based on p

Sponsors

The Second Affiliated Hospital of Hainan Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Gestational age and parity: Mothers of premature infants who delivered at 32 weeks <= gestational age <= 36?^6 weeks; 2. Neonatal condition: The newborn is transferred to the NICU within 24 hours after birth; 3. Diagnostic basis: The diagnostic criteria for preterm birth refer to the definition of preterm birth in the 9th edition of "Obstetrics and Gynecology", which is delivery at 28 weeks but less than 37 weeks of gestation; 4. Data integrity requirements: The research subjects should be able to cooperate in completing at least 4 group activities and follow-up evaluations at 1 month, 3 months, and 6 months postpartum; 5. Informed consent: The research participants themselves agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe physical illness of the mother: The mother of a premature infant suffers from severe diseases of the heart, brain, lungs, kidneys and other organs or other serious chronic diseases, and is unable to cooperate with the researchers; 2. Mother's mental or communication disorders: The mother has mental or language communication disorders and is unable to communicate normally and complete the questionnaire; 3. Severe illness of the mother: The mother is transferred to the intensive care unit for treatment due to the need for her condition after giving birth; 4. Severe diseases in premature infants: Premature infants who suffer from congenital genetic metabolic diseases, congenital malformations, and other diseases that require surgical operations; 5. Premature infants giving up treatment: Premature infants whose family members give up treatment; 6. Refusal of informed consent: Where a research participant or their legal representative refuses to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Breastfeeding self-efficacy;Parenting sense of competence;Anxiety symptoms;Maternal neonatal care ability;Edinburgh Postnatal DePression Scale;

Secondary

MeasureTime frame
Acceptability;Feasibility;Participation rate;Loss to follow-up rate;

Countries

China

Contacts

Public ContactChen Xiaojing

The Second Affiliated Hospital of Hainan Medical University

chenxj199929@163.com+86 898 8931190

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026