labor.
Conditions
Interventions
Intervention 1: Intervention group received routine intervention with a support person during labor. Routine intervention will be included monitoring of uterine contractions, bleeding, fetal medicals
Control group received routine intervention without a support person during labor. monitoring of uterine contractions, bleeding, fetal medicals care and other usual hospitals' medical cares and other
Intervention group received routine intervention with a support person during labor. Routine intervention will be included monitoring of uterine contractions, bleeding, fetal medicals care and other
Sponsors
Vice chancellor for research, Isfahan University of medical sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Singleton normal full-term pregnancy and desire to have natural vaginal delivery, 38 to 42 weeks of gestation, spontaneous onset of labor and normal birth with no special procedures or consultation, family or a female friend was available to stay in the hospital throughout the birth process. Exclusion criteria: Chose a caesarean section, cervical dilatation of more than four centimeters at the time of admission.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Length of stage of labor. Timepoint: During intervention. Method of measurement: Time of cervical dilation.;Cervical laceration. Timepoint: After intervention. Method of measurement: Yes / No.;Pain. Timepoint: Before and after intervention. Method of measurement: The numeric rating scale, between 0 (no pain) and 10 (worst pain). | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction. Timepoint: After intervention. Method of measurement: The numeric rating scale (between 0 and 100). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Shahshahan
Isfahan University of Medical Sciences
Outcome results
None listed