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The effect of delivery preparation consult on the pregnancy outcome and pregnant women’s satisfaction

The effect of delivery preparation consult versus routine pregnancy cares on the pregnancy outcome and pregnant women’s satisfaction in the Fatemieh Hospital in Hamadan

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015012513405N9
Enrollment
170
Registered
2015-05-19
Start date
2015-01-30
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

Pregnancy. Supervision of other normal pregnancy

Interventions

Experimental group: holding 8 session of consulting for pregnant women included nutrition, exercise, description about normal vaginal delivery etc, each taking 90 minutes
Intervention 1: Experimental group: holding 8 session of consulting for pregnant women included nutrition, exercise, description about normal vaginal delivery etc, each taking 90 minutes. Intervention
Prevention
Control group: routine pregnancy cares for pregnant women

Sponsors

Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Those women will be included who are certified by the physician to enjoy complete health; not being inflicted with a specific diseases such diabetes, cardio-vascular; their pregnancy will not be of high risk such as multi-twins, repeated abortion, placenta previa, preeclampsia; their gestational age will range from 20 to 23 weeks; having tendency to participate in educational classes; their previous delivery be NVD in the case of multipar women; and have not taken part in the similar educational classes. Exclusion criteria: Those women will be excluded who do not tend to participate in educational classes; make absence more than one session of consult; are not threatened by risk factors such as being conflicted with preeclampsia, amniotic fluid tear and preterm delivery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Birth weight. Timepoint: Immediately after delivery. Method of measurement: Weighing balance of infant's weight.;Choosing the type of delivery. Timepoint: 20th and 36th week of pregnancy. Method of measurement: Questionnaire.;The type of delivery. Timepoint: Immediately after delivery. Method of measurement: Questionnaire.;Satisfaction. Timepoint: Before the intervention, after finishing the consult sessions. Method of measurement: Questionnaire.;The weight increase of mother during pregnancy. Timepoint: 20th and 36th week of pregnancy. Method of measurement: Weighing balance.

Secondary

MeasureTime frame
Apgar score. Timepoint: Immediately after delivery. Method of measurement: Check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh Zahra Masoumi

Hamadan University of Medical Sciences

zahramid@yahoo.com; zahra.masoomi@umsha.ac.ir+98 81 3838 0150

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 11, 2026