Skip to content

Development and Evaluation of an Intervention to Optimize Women’s Childbirth Experience

Development and Evaluation of an Intervention to Optimize Women’s Childbirth Experience

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120687
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Delivery trauma

Interventions

Qualitative interviews with postpartum women, midwives, and physicians, and focus group discussions:None
Pilot Group:1. Antenatal Phase Intervention Location: Obstetric outpatient clinic or prenatal education classes Intervention Providers: Researchers and obstetric nurses Intervention Frequency: Four fa

Sponsors

Luoyang Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. The pregnant woman should be 18 years old or above, have full capacity for civil conduct and be able to sign the informed consent form independently. 2. At 12 to 20 weeks of pregnancy, there is a single pregnancy and the condition during pregnancy is stable. 3. Possess basic language communication skills, be able to understand and participate in the intervention and communication related to childbirth. 4. Have the willingness to participate in the delivery care intervention and be willing to complete the intervention and follow-up at each stage from pregnancy to postpartum in accordance with the research plan.

Exclusion criteria

Exclusion criteria: 1. There is a history of severe mental illness or cognitive impairment that affects participation in intervention or emotional expression. 2. Severe obstetric complications during pregnancy, such as amniotic fluid embolism, placental abruption, uterine rupture, severe gestational hypertension or diabetes, etc. 3. The risk of severe neonatal diseases or fetal malformations during pregnancy is high, which may affect the psychological state of the mother. 4. Having participated in other psychological intervention or birthing-related studies may interfere with the research results.

Design outcomes

Primary

MeasureTime frame
Edinburgh Postnatal Depression Scale (EPDS) Score;

Secondary

MeasureTime frame
Birth Experience and Psychological Status-related Characteristics;Birth Trauma-related Experiences and Influencing Factors;Perceived Participation and Control in Childbirth Process;Level of Negative Emotional Responses in Parturients;Development and Evaluation Results of Birth Trauma Nursing Intervention Program;

Countries

China

Contacts

Public ContactSun Yafang

Luoyang Maternal and Child Health Hospital

232730125@qq.com+86 137 8316 1646

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026