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Effects of the Collaborative Labor Accompaniment Model Involving Midwives and Spouses of Parturients on Labor Duration and Childbirth Experience in Primiparas with Full-Term Singleton Pregnancies

Effects of the Collaborative Labor Accompaniment Model Involving Midwives and Spouses of Parturients on Labor Duration and Childbirth Experience in Primiparas with Full-Term Singleton Pregnancies

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128369
Enrollment
Unknown
Registered
2026-07-19
Start date
2025-09-01
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Normal delivery

Interventions

Traditional delivery mode group:None
Midwife and parturient spouse collaborative companionship model group:None

Sponsors

HanDan Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Both the parturient and her husband are aged between 20 and 40 years (inclusive); 2.The subject is a primipara with a singleton cephalic fetus, gestational age at delivery greater than or equal to 37 weeks, normal external pelvic measurements, and no obvious cephalopelvic disproportion. 3.No severe maternal comorbidities or pregnancy complications. 4.Has the intention to undergo vaginal delivery, with no contraindications to vaginal delivery. 5.The parturient and her spouse are in good health, with full cognitive and behavioral capacity. 6.The spouse has been fully informed of this study and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.The pregnant woman has severe comorbidities or complications, such as pregnancy-induced hypertension, gestational diabetes mellitus, or hyperthyroidism that are not well controlled by medication; 2.The husbands of parturients in the intervention group did not participate in the entire delivery process. 3.The parturient was transferred to the ICU due to delivery complications such as severe postpartum hemorrhage. 4.Patients with fetal developmental abnormalities, malpresentation, contracted pelvis, intra-amniotic infection, amniotic fluid embolism, or suspected macrosomia. 5.Patients with indications for cesarean section.

Design outcomes

Primary

MeasureTime frame
Postpartum 2-Hour Blood Loss Volume;Apgar Score of Newborn;Postpartum Satisfaction;Duration of the first stage of labor;Duration of the second stage of labor;

Countries

China

Contacts

Public ContactZhang Yunjing

HanDan Central Hospital

15297524382@163.com+86 310 2118210

Outcome results

None listed

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