pain and experince of child birth.
Conditions
Interventions
Intervention 1: Intervention group: People who will receive the Swedish massage. Intervention 2: Intervention group: People who will receive the Interferential Electrical Stimulation. Intervention 3:
Sponsors
vice chancellor for reaserch, University Of Tabriz Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Being nulliparous Being Singleton Gestational age 38 to 40 weeks Being at the beginning of the active phase (dilatation 4 cm) cephalic presentation of fetus, Having a intact membranes, No Drug Addiction and Smoking, existence of low-risk pregnancy without medical complications in pregnancy, including hypertension, gestational diabetes, twins and multiple pregnancy , placenta and amniotic fluid disorders and ....
Exclusion criteria
Exclusion criteria: A history of chronic systemic, cardiac, pulmonary diseases according to the patient himself meconium-stained amniotic fluid before intervention Any skin problem in the areas of electrodes, existence any skin disorders and fractures in the site of massage Allergy to olive oil People receiving Painless delivery of medication (receiving epidural anesthetics and intravenous infusion of remifentanil) People receiving other non-pharmacological analgesics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| -Comparison of the mean score of labor pain among the study groups. Timepoint: Pain score in all three groups before intervention, then every hour until the second stage of labor and one hour after delivery. Method of measurement: Using the VAS scale( Visual Analogue Scale).;Comparison of mean score of labor experience among study groups. Timepoint: 12-24 hours after childbirth. Method of measurement: Using LAS (Labor Agentry Scale). | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of duration of active phase of labor among study groups. Timepoint: From the dilatation of 4 cm until the baby's exit, following the examinations performed by the researcher, the partograph graph will be filled and is drawn. Method of measurement: Using the Partograph.;Comparison of the mean of satisfaction score of delivery among the study groups. Timepoint: 12-24 hours after childbirth. Method of measurement: Using the Mackey Scale.;Comparison of fetal heart rate disorders among study groups. Timepoint: Each hour will be controlled by the researcher. Method of measurement: It will be recorded in the checklist.;Comparison of the Apgar score of the first and fifth minutes among the study groups. Timepoint: In the first and fifth minutes after childbirth. Method of measurement: It will be recorded in the checklist. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahin Kamalifard
Tabriz University of Medical Sciences
Outcome results
None listed