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

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015051822302N1

Enrollment

146

Registered

2015-10-18

Start date

2015-05-03

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

Cesarean. Other single delivery by caesarean section

Interventions

Intervention 1: Questionnaire to assess attitudes, expectations, outcome, impact evaluation, subjective norms, perceived behavioral control and intention to perform caesarean sections that are assesse

Behavior

Questionnaire to assess attitudes, expectations, outcome, impact evaluation, subjective norms, perceived behavioral control and intention to perform caesarean sections that are assessed for Likert res

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Kaboudi

Kermanshah University of Medical Sciences, School of Nursing and Midwifery

fkaboudi@kums.ac.ir+98 83 3827 9394

Outcome results

None listed

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