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The effect of motivational interview on the choice of delivery type in vaginal birth after cesarean delivery

The effect of motivational interview on preference of delivery in mothers with a history of previous cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201103049248N1
Enrollment
50
Registered
2023-04-17
Start date
2023-03-11
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

choosing the type of delivery.

Interventions

Intervention 1: Intervention group: In the intervention group, in addition to receiving routine pregnancy care, pregnant women participate in motivational interview sessions with 6 to 8 people. This i

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Having a history of at least one previous caesarean section. Absence of high-risk pregnancy items (history of infertility, gestational diabetes, pre-eclampsia, placenta previa, history of abortion and stillbirth, symptoms of threatened abortion). Absence of chronic diseases during pregnancy (blood pressure, diabetes, etc.) Gestation age 25 to 30 weeks. Having a singleton pregnancy.

Exclusion criteria

Exclusion criteria: Fear of childbirth or any phobia diagnosed by a psychiatrist Twin or multiple pregnancy Suffering from chronic diseases such as high blood pressure, diabetes, etc. Suffering from psychiatric diseases such as depression or suicidal thoughts

Design outcomes

Primary

MeasureTime frame
Birth preference. Timepoint: the beginning of the study (before the start of the intervention) and immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: Questionnaire of Hajian's birth type preference.

Secondary

MeasureTime frame
Perceived sensitivity. Timepoint: before the start of the intervention and immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: It is evaluated by the efficiency and behavioral intention of childbirth questionnaire, which includes 5 questions that are scored based on the Likert scale from 1 to 7.;Perceived intensity. Timepoint: before the start of the intervention and immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: It is evaluated by the efficiency and behavioral intention of childbirth questionnaire, which includes 5 questions that are scored on a Likert scale from 1 to 7.;Perceived effectiveness. Timepoint: before the start of the intervention and immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: It is evaluated by the efficiency and behavioral intention of childbirth questionnaire, which includes 6 questions that are scored on a Likert scale from 1 to 7.;Perceived self-efficacy. Timepoint: before the start of the intervention and immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: It is evaluated by the efficiency and behavioral intention of childbirth questionnaire, which includes 7 questions that are scored on a Likert scale from 1 to 7.;Consciousness. Timepoint: before the start of the intervention and immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: It is measured by the efficiency and behavioral intention of childbirth questionnaire, which includes 9 questions, the answers of which are natural childbirth, caesarean section, and I don't know.;Behavioral intention. Timepoint: before the start of the intervention and immediately after the end of the intervention and one month after the end of the intervention. Method of measureme

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtefeh Malvandi niko

Shahroud University of Medical Sciences

atefeh.niko1370@gmai.com+98 51 4446 0853

Outcome results

None listed

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