labor pain.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Low risk pregnancy Gestational age 37-40 Cephalic presentation Single pregnancy Entering the active phase of childbirth Have at least one healthy ear Being between 35-18 years old
Exclusion criteria
Exclusion criteria: Receiving analgesic drug within 3 hours before the start of the study. Use of oxytocin to induce and accelerate labor. Drug addiction. Being an athlete. History of infertility.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduce pain intensity. Timepoint: Prior to intervention, in cervical dilatation 4, 6 and 8 cm. Method of measurement: Visual Analogue Scale.;Reduce the duration of labor. Timepoint: Time interval from dilatation of cervix 4 to 10 cm. Method of measurement: In terms of hours, the time between dilatation is 4 cm to 10 cm of the cervix. | — |
Countries
Iran (Islamic Republic of)
Contacts
Kerman University of Medical Sciences