pregnancy. Supervision of normal pregnancy, unspecified
Conditions
Interventions
Intervention 1: The intervention in case group includes: Hiring a responsible midwife for every pregnant woman. This midwife is a member of management team and provides direct care during prenatal, de
The intervention in case group includes: Hiring a responsible midwife for every pregnant woman. This midwife is a member of management team and provides direct care during prenatal, delivery and postp
The control group will receive routine care. In routine method, pregnant women refer to health center. There is not responsible midwife or continuous relationship with care provider. Most of women are
Sponsors
Vice chancellor for research, Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: The Low risk pregnant women that: - Their gestational age is under fourteen weeks - They have not any diseases - They have not previous high risk pregnancy - They have not history for infertility - They have not previous cesarean section - They have not previous abdominal surgery Exclusion criteria: - Their pregnancy be high risk - They have no desire to continue staying in the study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maternal satisfaction. Timepoint: 1 month after intervention. Method of measurement: Questionnaire.;Maternal outcomes. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder and interview.;Neonatal outcomes. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Number of visits in pregnancy. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Number of sonography. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Fetal death before or after 24 weeks. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder and interview.;Hospitalization. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder and interview.;Bleeding before delivery. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder and interview.;Husband presence in visits. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder and interview.;Induction. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Physiologic delivery. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Analgesic and anesthesia. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Duration of labor. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Duration of hospitalization. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Delivery type. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Episiotomy. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder.;Perineal laceration. Timepoint: at the end of intervention. Method of measurement: observe the hospital folder and interview.;Gesta | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAzam Bagheri
Kashan University of Medical Sciences
Outcome results
None listed