MedPath

Effects of LI4 Acupressure on labor pain in the first stage of labor

Not Applicable
Conditions
labor pain.
Maternal distress during labour and delivery
Registration Number
IRCT138904104281N1
Lead Sponsor
Iran University of Medical Sceince and Health Services
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

Inclusion criteria included: first to third pregnancy, no drug addiction, gestational age more than 37 weeks, single fetus, cephalic presentation, age 40 to 20 years, no previous experience of using acupressure to each reason, absence of any wounds, bruising, irritation in sensitive estuary needle point LI4, no previous cesarean section.
Exclusion criteria: receiving sedatives or anesthesia during the study, any other intervention such as injecting drug oxytocin

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before intervention, immedietly after the intervention, 20, 60 minutes and every hour until onset of secondry stage of labor. Method of measurement: Visual Analog Scale.
Secondary Outcome Measures
NameTimeMethod
eonatal Apgar score. Timepoint: at the 1st and 5th minute. Method of measurement: Examination & Ovservation.;Memory of labor pain. Timepoint: 24 hours after delivery. Method of measurement: Visual Analog Scale.;Satisfaction from delivery. Timepoint: immediately after delivery. Method of measurement: scale ruler 6 parts.;Delivery type. Timepoint: after termination of pregnancy. Method of measurement: observation.;Duration of the first and second phases of labor. Timepoint: from 3-5 cm cervical dilation to full cervical dilatation and full cervical dilatation to the delivery time. Method of measurement: timer.
© Copyright 2025. All Rights Reserved by MedPath