Pain. Pain, not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Gestational age Between 37 and 42 weeks At least Diploma Literacy Singleton pregnancy 4 cm dilatation Low risk pregnancy (no rupture over 6 hours of water sac) Conscious consent of the individual to enter the study
Exclusion criteria
Exclusion criteria: Preterm delivery Third-trimester hemorrhage and intrauterine growth retardation Preeclampsia 24<BMI<18.5 History of acute and chronic pain such as migraine Performing professional exercise (due to changes in the threshold of pain and delivery phase) Drug Addiction, Alcohol and Smoking Receive analgesic within 3 hours before the onset of intervention History of allergy to herbal Diseases of internal and surgical diseases in mother and fetus Existence of fetal distress symptoms Clear stenosis in the pelvic floor Known mental disease Stay in active phase of labor Diabetes Seizure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in pain. Timepoint: Before the beginning of the study, at dilates 6-4, 8-6, 10-8 cm and immediately after intervention. Method of measurement: VAS. | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction Survey. Timepoint: End of research. Method of measurement: questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Bojnourd University of Medical Sciences