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

This trial accepts healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • 4-step narrative nursing program

    Behavioral

    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.

Treatment groups

160 Participants
are divided into 2 treatment groups
Group A: Routine perinatal careNo intervention 0 interventions
Group B: 4-step narrative nursingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Postpartum anxiety at 48 hours

Mean score on the State-Trait Anxiety Inventory (STAI-State, 20 items) assessed 48 hours after cesarean delivery. Lower scores indicate less anxiety.

Time frame
48 hours post-surgery

Secondary outcomes

1

Postpartum depression risk

Proportion of women with Edinburgh Postnatal Depression Scale (EPDS) ≥ 10 at 48 hours, 2 weeks and 3 months.

Time frame
48 hours, 2 weeks, 3 months postpartum
2

Breastfeeding self-efficacy

Mean score on the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF, 14 items) at 48 hours, 2 weeks and 3 months. Higher scores indicate greater confidence.

Time frame
48 hours, 2 weeks, 3 months postpartum
3

Pain intensity

Mean Numerical Rating Scale (NRS, 0-10) for self-reported pain at 48 hours and 2 weeks.

Time frame
48 hours and 2 weeks postpartum
4

Breastfeeding continuation rate

Percentage of women who report any breastfeeding at 3 months.

Time frame
3 months postpartum

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Xi Huang

Lead sponsor

Xiamen University

Sponsor institution

Xiamen University

Collaborator

Yilong People's Hospital

Collaborator