Evaluation of continuous support by dula midwife on labor process
Not Applicable
- Conditions
- labor care Method.
- Registration Number
- IRCT20140924019277N2
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 110
Inclusion Criteria
all primiparous women with term , live and singleton fetus cephalic presentation and estimated fetal weight of 2500-3400 g,
Exclusion Criteria
patients with any chronic or mental illness, pregnancy disorders, the possibility of the narrow pelvis, a history of any kind of scar on the uterus, abnormal bleeding, fetal anomalies, fetal distress, and any kind of clear Caesarean induction. , the applicant or recipient of spinal or epidural anesthesia, withdraw from the study at any time
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity. Timepoint: every 3 hour. Method of measurement: Visual analog pain scale.;Labor duration. Timepoint: from the moment of admission [active phase beginning 2-3 houre and for the second and third stages separately from the beginning to the end of each stage. Method of measurement: vaginal exam and record.;Delivery method. Timepoint: in the end of delivery. Method of measurement: observatio.
- Secondary Outcome Measures
Name Time Method