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The effect of physiological birth on reduction of cesarean delivery

Effect of education of physiological delivery in reducing the cesarean rate in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014072713405N4
Enrollment
160
Registered
2014-11-14
Start date
2014-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Relationship between education of physiological delivery and reducing cesaren birth. Pregnancy, childbirth and the puerperium

Interventions

Intervention 1: Intevention group: physiological birth. Intervention 2: Control group: Routine normal delivery.
Prevention
Intevention group: physiological birth
Control group: Routine normal delivery

Sponsors

Vice chancellor for Research the Technology, Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:No prohibition of normal vaginal delivery; no known physical and mental illness; the absence of high risk pregnancy for example blood pressure 140.90 and higher, preeclampsia, polyhydramniosis and oligohydramniosis; absence of cesarean section history or any uterine scar and placenta previa; Lack of prolonged rupture of membranes more than 18 hours before delivery; estimation of fetal weight between 2500-4000 gr; absence of fetal congenital anomalies identified by ultrasound in perinatal Exclusion criteria:Blood pressure 140.90mmHg and higher during the intervention; failure to attend more than one session of training

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Type of delivery. Timepoint: Immediately after delivery. Method of measurement: Questionnaire.;Fear of delivery. Timepoint: Before education and after delivery. Method of measurement: Questionnaire.;Pain of delivery. Timepoint: After delivery. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Apgar. Timepoint: After delivery. Method of measurement: Check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh Zahra Masoumi

Hamedan University of Medical Sciences

zahramid2001@yahoo.com; zahra.masoomi@umsha.ac.it+98 81 3838 0150

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026