Evaluation of the effect of prostration on pain and delivery time
Not Applicable
Recruiting
- Conditions
- Duration of labor and pain intensity in nulliparous women.
- Registration Number
- IRCT20200415047087N2
- Lead Sponsor
- Jeeroft University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
Single pregnant women with fetal cephalic screening,
Term and low-risk pregnancies
No rupture of the bladder for more than 12 hours
Having spontaneous contractions and dilation of 4 cm of the cervix
Estimated fetal weight between 4000-2500 grams
Evidence of fetal health based on ultrasound findings
Not attending childbirth preparation classes
No known chronic diseases
No mental and anatomical disorders
Exclusion Criteria
Exclude if you use painkillers or labor stimulants
Withdrawal from labor and natural childbirth such as decolonization, umbilical cord prolapse and fetal distress
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity: The score that a person expresses according to the visual scale of pain, the intensity of her pain. Timepoint: Measure the severity of pain twice: before the intervention and after the intervention. Method of measurement: By asking the mother and using the visual pain scale.;Duration of labor: Based on the standard partograph form in the women's file, the progress and duration of labor are determined. Timepoint: After the intervention. Method of measurement: Partograph form.
- Secondary Outcome Measures
Name Time Method