None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The desire to participate in the study Women aged 40-18 Pregnancy age between 42-37 weeks 4-3 cm dilatation At least reading and writing skills Having a natural garden before studying Not having a midwife along Exposure to the embryo Not having diseases like cancer, lumbar disc disease, high blood pressure, seizures, diabetes, high fever, infectious disease,
Exclusion criteria
Exclusion criteria: Rupture more than 6 hours a bottle of water Get anorexia three hours before the study begins Multiplayer women Known mental illness Surgery of the spine in the last three months The occurrence of any stressful event involving the separation of the spouse, the death of the loved ones within the past six months Drug Addiction and Psychosocial History of sensation and allergy to fragrances Third-trimester bleeding Abortion history
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The severity of labor pain is measured based on a pain reliever. Timepoint: -In dilates of 5-4, 7-6 and 8-10 cm cervix before and after intervention in the studied groups. Method of measurement: Based on the visual scale of the pain, which is a 10-cm ruler, the zero number on the left indicates no pain and the number 10 on the right. | — |
Countries
Iran (Islamic Republic of)
Contacts
Sanandaj University of Medical Sciences