Assessment of designed educational program on cesarean intention among nulliparous pregnant wome

Phase 2

• Conditions: Cesarean.; Other single delivery by caesarean section

• Registration Number: IRCT2015051822302N1
• Lead Sponsor: Vice Chancellor for research Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 146

Inclusion Criteria

aged between 18 to 35 years? gestational age 28 weeks and more? first pregnancy? do not have anxiety disorder and other mental disorders and do not have medical indication for cesarean delivery include multi gestation? Placenta previa? hysterotomy? breech presentation? preeclampsia.
Exclusion criteria:participate in the preparation childbirth class? lack of consent to participate in all training session.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cesarean intention. Timepoint: Before and 4 weeks after the end of intervention. Method of measurement: Questionnaire created by the resecher.;Attitude. Timepoint: Before and 4 weeks after the end of intervention. Method of measurement: Questionnaire created by the resercher.;Outcome expectations. Timepoint: Before and 4 weeks after the end of intervention. Method of measurement: Questionnaire created by the resecher.;Outcome expectancy. Timepoint: Before and 4 weeks after the end of intervention. Method of measurement: Questionnaire created by the resercher.;Subjective norms. Timepoint: Before and 4 weeks after the end of intervention. Method of measurement: Questionnaire created by the resercher.;Perceived behavioral control. Timepoint: Before and 4 weeks after the end of intervention. Method of measurement: Questionnaire created by the resercher.