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Effects and Childbirth Experience Between Zhang and WHO Partograph

The Effect Of Zhang's Guidelines Versus Who Partograph On Childbirth Experience According To Ceq-My

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07121491
Enrollment
713
Registered
2025-08-13
Start date
2024-06-27
Completion date
2025-02-28
Last updated
2025-08-13

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

Conditions

Childbirth Experience, Outcome, Adverse Birth

Keywords

Labour outcome, Childbirth experience

Brief summary

This study compared the labour outcomes and childbirth experience between Zhang and WHO partograph.

Detailed description

A prospective cross-sectional observational study that compared the cervical os dilatation i.e 4 and 6 cm upon admission to the labour room. Eligible patients were recruited during postnatal period in the ward before discharged home. The details of clinical characteristics and labour outcomes were collected. Patients then answered the CEQ-My questionnaire form that assess their childbirth experiences. The primary outcome measure was caesarean section rate and the secondary outcome measure was the childbirth experience.

Interventions

None listed

Sponsors

National University of Malaysia
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* cervical dilatation 4 or 6 cm * singleton * cephalic presentation * at 37 weeks or more * normal cardiotocograph tracing on admission * understands Malay or English * no uterine scar * no pre-existing medical disorders * no antenatal complications such as diabetes or hypertension

Exclusion criteria

* multiple pregnancy * none cephalic presentation * abnormal admission cardiotocograph tracing * less than 37 weeks gestation * refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Caesarean section ratefrom cervical dilatation of 4 or 6 cm through study completion up to delivery of the foetusRate of delivery via caesarean section in percentage

Secondary

MeasureTime frameDescription
Childbirth experiencefrom Day 1 throughout study completion, an average of 7 days after deliveryAssessment of experience during delivery using questionnaire based on based on total childbirth experience questionnaire score using Likert scale from 1 to 4. Score of 4 is a total agreement and score of 1 is total disagreement.

Other

MeasureTime frameDescription
Duration of hospital stayFrom predelivery throughout study completion, an average of 5 daysDuration from admission until discharge either 3 days or less or more than 3 days
Use of analgesiaFrom cervical dilatation of 4 or 6 cm until delivery of fetusNumber of patients needed analgesia in percentage
Apgar score at 5 minutesFrom delivery of neonate until 5 minutes after deliveryNeonatal Apgar score less than 7 at 5 minutes after delivery based on the Apgar score with 0 the lowest and 10 the highest
Admission into neonatal care intensive unitFrom birth of the neonate until throughout study completion, an average of 7 days after birthNumber of neonates needed to be admitted into neonatal care intensive unit
Oxytocin useFrom cervical dilatation of 4 or 6 cm until delivery of fetusNumber of women who needed oxytocin infusion

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026