Narrative Nursing for Cesarean Mothers' Anxiety and Breastfeeding Confidence

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorXi Huang

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • 4-step narrative nursing program

Treatment groups

160 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Xi Huang

Lead sponsor

Xiamen University

Sponsor institution

Xiamen University

Collaborator

Yilong People's Hospital

Collaborator