Skip to main content
Clinical Trials/IRCT2016060828352N1
IRCT2016060828352N1
Completed
Phase 3

The effect of couples counseling based on problem solving approach on the childbirth fear, childbirth self-efficacy and the choice of the type of delivery in primigravid women requesting elective cesarean section

Chancellor for Research and Technology of Zanjan University of Medical Sciences0 sites76 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Condition 1: Elective cesarean. Condition 2: Single spontaneous delivery.
Sponsor
Chancellor for Research and Technology of Zanjan University of Medical Sciences
Enrollment
76
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Chancellor for Research and Technology of Zanjan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Being primigravida; No history of infertility based on mother's report; Singleton pregnancies; Being in 28 to 32 weeks of pregnancy based on the first day of the last menstrual period or sonographic assessment before 12 weeks of gestation; Lack of any obstetric complications in the current pregnancy according to mother's report (preeclampsia, gestational diabetes, placenta previa, etc.); Not participation in the counseling classes at the same time; No indication for cesarean delivery; Lack of a history of physical and mental diseases in couples based on mother's report (hypertension, diabetes, using psychiatric drugs, history of hospitalization for various reasons ...); Complete satisfaction for participation in the study.
  • Exclusion criteria: any abnormal condition before the onset of labor which prevents the normal delivery such as bleeding and placental abruption (premature separation of the placenta from the uterine wall); Difficult or impossible access to participant because of changing the living place; Lack of consent to continue participation in the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials