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Effect of rereading of written scenario on selection of delivery method

Clinical trial of comparing effectiveness of "rereading of written scenario" and "theory of planned behavior" with a group without any intervention on selection of delivery method in nulliparous pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015052020706N2
Enrollment
213
Registered
2015-08-29
Start date
2015-05-22
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

Delivery. Single spontaneous delivery, Single delivery by caesarean section

Interventions

Behavior
Intervention 1: The control group received no intervention. This group includes 71 nulliparous pregnant women. The delivery type inventory according to theory of planned behavior and also pregnancy s
The control group received no intervention. This group includes 71 nulliparous pregnant women. The delivery type inventory according to theory of planned behavior and also pregnancy self-efficacy sc
The first intervening group (rereading of written scenarios based on the theory of planned behavior) comprises of 71 nulliparous pregnant women, who receive 3 sessions of 120 minutes with sequence of
The second intervening group (theory of planned behavior group) comprises of 71 nulliparous pregnant women, who receive 3 sessions of 120 minutes with sequence of once a week during28-32th week pregna

Sponsors

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

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Primigravida; pregnancy age:28-32 weeks; age of mother: 18-35 years; singleton pregnancy, having educational degree higher than a fifth grade of primary school, lack of repeated miscarriages, placenta previa and a ban on normal childbirth, lack of history for mental and physical diseases, non- smoking and drug abuse. Exclusion criteria: Those women will be excluded who do not tend to participate in educational classes, are absent in any of sessions of consultation, are not threatened by risk factors such as being conflicted with preeclampsia and preterm delivery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Delivery mode. Timepoint: After intervention and Immediately after delivery. Method of measurement: Percent.;Childbirth Self-Efficacy. Timepoint: before the intervention at 28-32 weeks and after the intervention at 37-40 weeks of pregnancy. Method of measurement: childbirth self-efficacy questionnaire.

Secondary

MeasureTime frame
The score of knowledge. Timepoint: before the intervention at 28-32th week of pregnancy and after the intervention at 37-40th week of pregnancy. Method of measurement: Questionnaire.;The scores of attitude. Timepoint: before the intervention at 28-32th week of pregnancy and after the intervention at 37-40th week of pregnancy. Method of measurement: Questionnaire.;The scores of Perceived behavioral control. Timepoint: before the intervention at 28-32th week of pregnancy and after the intervention at 37-40th week of pregnancy. Method of measurement: Questionnaire.;The scores of Subjective norms. Timepoint: before the intervention at 28-32th week of pregnancy and after the intervention at 37-40th week of pregnancy. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMassome Rasoli

Shahroud University of Medical Sciences and Health Services

massomerasoli@shmu.ac.irmassomerasoli@gmail.com+98 23 3239 5054

Outcome results

None listed

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