Effects of Pilates Ball and Sacral Massage Applications on Labor Pain, Labor Duration and Childbirth Satisfaction

Recruiting now · Not applicable

Conditions studied: Labor Pain, Satisfaction

In brief

As researchers, we believe that Pilates ball and manual sacral massage applications can be easily and cost-free applied in maternity clinics in our country. For all these reasons, this study was planned as a randomized controlled study to evaluate the effects of Pilates ball and sacral massage applications in labor on labor pain, labor duration, and labor satisfaction. The research will be carried out between December 1, 2024 and May 1, 2025 in two public hospitals affiliated with the Gaziantep Provincial Health Directorate. The sample of the research will consist of 35 pregnant women in the Pilates ball group, 35 in the sacral massage group and 35 in the control group, totaling 105 pregnant women who meet the criteria for inclusion in the research. Applications to the intervention groups will be made during the active phase of labor. Personal Information Form, Labor Monitoring Form, Application Monitoring Form to record the number and duration of applications, Visual Analog Scale to assess labor pain, Partograph to assess labor duration and Labor Satisfaction Scale to assess maternal satisfaction will be used in data collection. Data will be analyzed with tests appropriate to normal distribution characteristics in the SPSS 24 package program. At the end of the research, the effects of Pilates ball and sacral massage applications in labor on labor pain, labor duration and labor satisfaction will be evaluated.

Key facts

Study ID

NCT06927531

Run by

Ege University

People needed

105

Starts

2025-02-20

Expected to finish

2025-12-30

Last updated by the study team

2025-04-15

Who can join

Age: 18 and older, up to 35. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Pregnant women over 18 years old and under 35 years old
• Term pregnancies (38-41 weeks gestation)
• Primiparous
• Those with a single live fetus
• Vertex development
• Those who do not have any risk factors during pregnancy (Dermatological disease, Preeclampsia, active membrane rupture, oligohydramnios and polyhydramnios, gestational diabetes, placental anomalies, intrauterine growth retardation, intrauterine dead fetus, macrosomic babies, fetal distress, etc.)
• Those who do not have any obstacles for Pilates ball application
• Those who do not have any chronic diseases (Hypertension, DM, ...)
• Those in the active phase of labor, those who have at least 1 hour of labor follow-up
• Pregnant women who voluntarily accept to participate in the study

You may not qualify if…

• Indications for Caesarean section (such as presentation disorder, breech presentation)
• Those who underwent induction
• Those whose labor duration was shorter than 1 hour or longer than 8 hours
• Those who underwent vacuum forceps or shoulder insertion

Where it is running

• Gaziantep Unıversity — Şehitkamil, Gazi̇antep, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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