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Recruiting NCT07272252

Narrative Nursing for Cesarean Mothers' Anxiety and Breastfeeding Confidence

No phase Interventional Postpartum Anxiety Postpartum Depression (PPD) Breastfeeding Self-Efficacy Cesarean Section Wound

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: 4-step narrative nursing program.
Who it may be relevant to
Registry conditions: Postpartum Anxiety, Postpartum Depression (PPD), Breastfeeding Self-Efficacy, Cesarean Section Wound. Basic parameters: 18 years — 50 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Psychological Effects and Breastfeeding Self-Efficacy of a Structured Four-Step Narrative Nursing Intervention in Cesarean Mothers: A Randomized Controlled Mixed-Methods Study

Overview

This study tests whether a nurse-led "4-step narrative nursing" program can reduce anxiety and improve breastfeeding confidence in mothers who are having a planned or non-emergency cesarean section. What is the problem? About 30-40% of Chinese cesarean mothers feel high anxiety after surgery, and 1 in 5 is at risk for postpartum depression. Low confidence in breastfeeding is also common. What will we do? We will randomly assign 160 mothers (1:1) to either: Usual care - standard education and ward care, or Usual care plus narrative nursing - four short (10-20 min) conversations with a trained nurse: Before surgery - help the mother talk about her fears. 24-48 h after surgery - encourage her to "name" pain or worries and separate them from herself. Before discharge - guide her to find positive moments and build a "strong-mom" story. Two weeks later by phone - strengthen the new story and review feeding success. What will we measure? Main result: anxiety score at 48 h (STAI scale). Other results: depression risk, breastfeeding confidence, pain, and feeding rates up to 3 months. Possible benefits: Lower anxiety, better mood, higher breastfeeding rates. No drugs or extra procedures are involved, only talking. Risks: Minimal; some mothers may feel emotional during conversations, but nurses can pause or refer to counselling if needed.

Interventions

  • Behavioral 4-step narrative nursing program
    Four nurse-led storytelling sessions (pre-operative externalization, post-operative deconstruction, pre-discharge reconstruction, and 2-week meaning-reconstruction phone call) aimed at reducing anxiety and increasing breastfeeding self-efficacy.

Primary outcome measures

  • Postpartum anxiety at 48 hours [Time frame: 48 hours post-surgery]
Secondary outcome measures (4)
  • Postpartum depression risk [Time frame: 48 hours, 2 weeks, 3 months postpartum]
  • Breastfeeding self-efficacy [Time frame: 48 hours, 2 weeks, 3 months postpartum]
  • Pain intensity [Time frame: 48 hours and 2 weeks postpartum]
  • Breastfeeding continuation rate [Time frame: 3 months postpartum]

Eligibility criteria

Inclusion criteria

  • Women aged 18-50 years
  • Scheduled for elective or non-emergency cesarean section at ≥37 weeks
  • Able to communicate in Mandarin and provide written informed consent
  • Expected hospital stay ≥24 h
  • Singleton pregnancy with stable maternal and neonatal condition allowing routine mother-baby contact

Exclusion criteria

  • Severe psychiatric disorders (schizophrenia, bipolar disorder, active suicidal ideation)
  • Maternal or neonatal need for ICU/NICU admission
  • Emergency cesarean section preventing baseline assessment
  • Communication or cognitive impairment precluding interview

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

China · 1 center
  • Yilong County Maternal and Child Health Hospital — Nanchong

Identifiers

NCT: NCT07272252 · XMUNARRCARE2025 · FJ2022B061 · XMSHLXH2320 · Basic Nursing II

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗