Impact of Scheduled Maternal Position Changes Using a Peanut Ball on Labor Outcomes in First-Time Mothers Receiving Epidural Analgesia
Led by Hamad Medical Corporation · Updated on 2026-01-12
110
Participants Needed
1
Research Sites
8 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating whether using a peanut birthing ball with scheduled maternal position changes during labor can improve outcomes for first-time mothers receiving epidural analgesia. The study aims to determine if this approach can reduce the duration of the first and second stages of labor and affect the mode of delivery as well as maternal and newborn health. This is a non-invasive, randomized controlled trial conducted at the Womens Wellness and Research Center in Qatar.
Participants will be randomly assigned to one of two groups. The intervention group will receive scheduled position changes using a peanut birthing ball placed between the legs, with positions including left lateral, right lateral, semi-sitting, and Taylor positions, changed every 30-60 minutes under staff supervision. The control group will receive standard labor care without the use of the peanut ball or structured position changes.
During the study, participants will be closely monitored with continuous fetal and maternal assessments. Researchers will record labor duration, delivery type, oxytocin use, blood loss, perineal trauma, and hospital costs. Newborn assessments will include Apgar scores, NICU admission, birth injuries, and umbilical cord blood pH. Data will be collected in real time and analyzed to compare outcomes between groups, aiming to inform best practices for labor care with epidural analgesia.
CONDITIONS
Brief Title
Scheduled Positioning With a Peanutball(SPP) on Labor Outcomes Among Primiparous Women Under Epidural Analgesia
Research Team
P
Parveen N Nather, Master's in nursing
D
Dr.Ananth Nazarene, PHD in Nursing
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Suspected fetal macrosomia with mechanical obstruction concerns
Multiple gestation with complications
Severe orthopedic or musculoskeletal conditions preventing safe sitting or balance
High-risk pregnancy conditions such as uncontrolled gestational diabetes or hypertension
Conditions requiring continuous monitoring or restricted mobility
Inability to follow instructions or unsteady balance
Lack of trained staff for supervision during labor use
Use of unstable or improperly sized birthing ball
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Labor with Scheduled Positioning Using a Peanut Ball
Duration - Duration of labor (approximately 12 to 19 hours)
Participants receive epidural analgesia during labor and are positioned at scheduled intervals using a peanut birthing ball to support labor progress and maternal comfort. Positions include left lateral, right lateral, semi-sitting, and Taylor positions, supervised by trained staff.
Continuous in-hospital monitoring during labor
Standard Labor Care
Duration - Duration of labor (approximately 12 to 19 hours)
Participants receive standard intrapartum care with epidural analgesia without scheduled positioning or peanut ball use.
Continuous in-hospital monitoring during labor
Post-Delivery Observation
Duration - Up to 3 hours after delivery
Participants and newborns are observed after delivery to monitor outcomes including postpartum hemorrhage, perineal trauma, Apgar scores, and neonatal intensive care admission.
1 to 2 visits (in-hospital)
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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Published Research Related To This Trial
Influence of Laboring People's Mobility and Positional Changes on Birth Outcomes in Low-Dose Epidural Analgesia Labor: A Systematic Review with Meta-Analysis.
Maite de Verastegui-Martín, Ana de Paz-Fresneda, José Antonio Jiménez-Barbero...
Using a peanut ball during labour versus not using a peanut ball during labour for women using an epidural: study protocol for a randomised controlled pilot study.