Peanut ball may speed up labor for moms with epidurals
NCT ID NCT07333209
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether using a peanut-shaped birthing ball during scheduled position changes can help first-time mothers who have epidural pain relief have a shorter and safer labor. About 110 low-risk women in Qatar will be randomly assigned to either use the peanut ball or receive standard care. Researchers will compare labor length, delivery method, and health outcomes for both mothers and newborns.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 110 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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16 to 55 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria:Inclusion Criteria: To be eligible for participation, women must meet all the following criteria: * Primiparous (first pregnancy resulting in a live birth or stillbirth after 20 weeks of gestation). * Singleton at gestation. * Gestational age of the term (37 weeks 0 days to 41 weeks 6 days). * Admitted to the Labor and Delivery Unit at WWRC in active labor. * Received epidural analgesia for labor pain management. * Expected to have a vaginal delivery (e.g., no contraindications for vaginal birth identified at the time of recruitment). * Able to understand and communicate in Arabic or English. * Provide written informed consent. Exclusion Criteria:The birthing ball should NOT be used in any of the following conditions: 1. Obstetric Contraindications (Maternal) * Any situation where vaginal birth is not appropriate (e.g., absolute indication for cesarean section) * Non-progress of labor requiring immediate intervention * Severe pre-eclampsia/eclampsia * Active vaginal bleeding of unknown cause * Placenta previa (major) or vasa previa * Placental abruption (suspected or confirmed) * Preterm labor with medical contraindication to ambulation or mobility * Ruptured membranes with unstable fetal head (high station) → Risk of cord prolapse * Severe maternal exhaustion requiring bed rest * Maternal hemodynamic instability 2. Fetal Contraindications * Non-reassuring fetal heart rate requiring continuous monitoring (Category II-III tracings) * Malpresentation requiring immediate obstetric intervention (e.g., transverse lie) * Suspected macrosomia with mechanical obstruction concerns (e.g., cephalopelvic disproportion) * Multiple gestation with instability or complications 3. Orthopedic / Musculoskeletal Contraindications * Any condition that prevents safe sitting, balancing, or weight-bearing, such as: Severe hips, leg, knee, or pelvic injuries * Significant arthritis of the lower limbs or pelvis * Recent joint surgery (hip/knee replacement, pelvic repair) * Neuromuscular disorders affecting balance (e.g., severe neuropathy) * Severe sciatica limiting mobility * Poor trunk control or inability to maintain safe seated posture 4. High-Risk Pregnancy Conditions * Use of birthing balls is contraindicated if pregnancy is classified as high-risk, including Uncontrolled gestational diabetes and Uncontrolled hypertension * Intrauterine growth restriction with required continuous monitoring * Polyhydramnios or severe oligohydramnios (risk of cord compression/instability) * Preterm premature rupture of membranes (PPROM) * History of preterm birth with current instability * Any condition requiring bed rest or reduced mobility 5. Safety / Environmental Contraindications * Patients are unable to follow instructions or unsteady balance * No trained staff available to supervise during labor use Unstable or improperly sized birthing ball
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Women's Wellness and research center
RECRUITINGDoha, Baladiyat ad Dawhah, 3050, Qatar
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Other studies related to the condition(s) this trial covers.
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