labor pain
Conditions
Interventions
This is a randomized clinical trial, without blinding of those involved in women in labor. The intervention group received inhalation of 3 drops of Lavandula angustifolia essential oil diluted in grap
Sponsors
Universidade do Sul de Santa Catarina
Universidade do Sul de Santa Catarina
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Pregnant women; primiparous; active labor
Exclusion criteria
Exclusion criteria: required cesarean section; glucocorticoids use in the last 30 days;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Around 30% of reduction in the average pain score in the intervention group compared to the control group. Assessed by the Visual Analog Scale (score from 0: no pain, to 10: worst pain). Data collected hourly from the start of active labor to the birth of the baby. | — |
Secondary
| Measure | Time frame |
|---|---|
| 20% increase in the mean birth satisfaction score in the intervention group compared to the control group. Evaluated by the Questionnaire of Experience and Satisfaction with Childbirth (QESP). Data collected between 24 to 36 hours from the birth of the baby. | — |
Countries
Brazil
Contacts
Public ContactAnna Piovezan
Universidade do Sul de Santa Catarina
Outcome results
None listed