About this trial
The study will be conducted with pregnant women in the active and transitional phases of labor. In the intervention group, sacral pressure will be applied during contractions, while the control group will receive routine clinical care. Perceived labor pain and maternal satisfaction will be assessed throughout the labor process
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Aged 18 years or older
Singleton pregnancy
Cephalic (vertex) presentation
Gestational age between 37 and 42 weeks
Disqualifiers
Illiterate in Turkish
Presence of chronic disease(s)
Trial design
Sequential
Treatments tested in this trial
manual pressure application
Other interventionPressure application using the metacarpal bone of one hand on the S4-S5 bones was planned.
Treatment groups
Trial outcomes
Primary outcomes
The VAS Pain Scale
Secondary outcomes
The Intrapartum Period Satisfaction Form
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: