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Cesarean rate reduction model

Designing of educational,financial and revisional interventions of human factors and structural agents on cesarean rate reduction ,administration and evaluation of them in Shahroud and comparison with cesarean rate in adjucent cities

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201106215525N2
Enrollment
220
Registered
2011-06-27
Start date
2010-12-22
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

Factors influencing health status and contact with health services. Supervision of normal pregnancy

Interventions

Intervention 1: Intervention in experiment group: 1- Prenatal educations mainly based on "Extended Parallel Process Model" are an essential intervention that will be given to 220 participants through
Prevention
Intervention in experiment group: 1- Prenatal educations mainly based on "Extended Parallel Process Model" are an essential intervention that will be given to 220 participants through 8 sessions. Thi
Participants in control group will not be educated likewise the intervention group on the basis of foregoing Model and will be given routine care

Sponsors

Vice chancellor for research, Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include: No history of former cesarean of uterine surgery, general wellbeing with no indication for medical/surgical intervention , Persian literacy 4- singleton pregnancy and cephalic presentation , No scientific approved indication for cesarean surgery , Being at 18 gestational weeks , singleton pregnancy and cephalic presentation Exclusion criteria conclude: Every induced systemic disease during present pregnancy which needs to medical or surgical intervention, and every obstetrical/non obstetrical indication for cesarean section

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cesarean delivery. Timepoint: at the end of study. Method of measurement: calculating.

Secondary

MeasureTime frame
Self efficacy. Timepoint: before and after prenatal educations. Method of measurement: questionnaire.;Knowledge. Timepoint: before and after prenatal educations. Method of measurement: questionnaire.;Intention. Timepoint: before and after prenatal educations. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSepideh Hajian

Shahroud University of Medical Sciences

hajian74@yahoo.com+98 912 383 7649

Outcome results

None listed

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