Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
Healthy Volunteers
ID06927531

Effects of Pilates Ball and Sacral Massage Applications on Labor Pain, Labor Duration and Childbirth Satisfaction: A Randomized Controlled Study

Led by Ege University · Updated on 2025-04-15

105

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the effects of Pilates ball exercises and manual sacral massage during labor on labor pain, labor duration, and childbirth satisfaction. The study is a randomized controlled trial that includes 105 pregnant women divided equally into three groups: Pilates ball, sacral massage, and a control group with no intervention. The investigation is motivated by the need for low-cost, non-invasive methods to help manage labor pain and improve childbirth experience, especially methods that can be easily applied in maternity clinics. During the active phase of labor, women in the sacral massage group will receive effleurage and vibration techniques on the sacral region once every hour for up to 10 minutes. Those in the Pilates ball group will perform pelvic oscillation movements on a ball, such as hip rotations and gentle bouncing, once an hour during labor. The control group will receive standard care without additional interventions. The study will be conducted between December 2024 and May 2025 at two public hospitals. Participants will be assessed using various tools, including a Visual Analog Scale for pain intensity, Partograph to monitor labor duration, and a Labor Satisfaction Scale to measure maternal satisfaction. Data collection involves forms to record personal information, labor progress, and intervention details. Researchers will analyze the data to determine how these non-pharmacological methods affect labor outcomes. The study period includes labor monitoring and post-intervention satisfaction evaluation.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women aged 18 to 35 years
  • Term pregnancies between 38 and 41 weeks gestation
  • First pregnancy (primiparous)
  • Single live fetus in head-down (vertex) position
  • No risk factors during pregnancy such as dermatological disease, preeclampsia, active membrane rupture, oligohydramnios, polyhydramnios, gestational diabetes, placental anomalies, intrauterine growth retardation, intrauterine fetal death, macrosomia, or fetal distress
  • No obstacles to Pilates ball application
  • No chronic diseases such as hypertension or diabetes
  • Currently in active labor with at least 1 hour of labor monitoring
  • Voluntary agreement to participate in the study
Not Eligible

You will not qualify if you...

  • Indications for cesarean section such as abnormal fetal presentation or breech position
  • Labor induced by medical procedures
  • Labor lasting less than 1 hour or more than 8 hours
  • Use of vacuum, forceps, or shoulder dystocia during delivery

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - During the active phase of labor (up to 8 hours)

Participants receive Pilates ball exercises or sacral massage during the active phase of labor, or receive routine care in the control group. These interventions aim to reduce labor pain and duration and improve childbirth satisfaction.

1 labor visit with hourly interventions or routine care

Follow-up

Duration - Immediately after labor

Participants' labor pain intensity, labor duration, and childbirth satisfaction are assessed after delivery.

1 post-labor assessment visit

Trial Site Locations

Total: 1 location

1

Gaziantep Unıversity

Şehitkamil, Gazi̇antep, Turkey (Türkiye)

Actively Recruiting

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Research Team

E

EMİNE CAN, ARAŞTIRMA GÖREVLİSİ

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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Published Research Related To This Trial

Effectiveness of sacral massage during labor in pregnant women: A systematic review and meta-analysis.

Somayeh Makvandi, Zahra Hadizadeh-Talasaz, Seyedeh Fatemeh Nosrati Hadi Abad...

https://pubmed.ncbi.nlm.nih.gov/39673988

Effect of using a birth ball on birth satisfaction and pain in pregnant women during labor: a randomized controlled trial.

Yasemin Erkal Aksoy, Sema Dereli Yilmaz, Şerife Çelimli

https://pubmed.ncbi.nlm.nih.gov/39585392