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CompletedNCT07889700BALL-USGUpdated Oct 22, 2026

Effect of Birth Ball Exercise on Labor Progress During the Active Phase of Labor Assessed by Intrapartum Ultrasound

An interventional study of Birth Ball Exercise in Labor and Labor Progress, sponsored by Sakarya University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Sakarya University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Nov 2025, registered May 2026).
Updated Oct 22, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
77
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Female
01

Study summary

The active phase of labor is a critical period for the progress of labor and maternal comfort. Non-pharmacological interventions such as birth ball exercises are frequently used to support labor progress and maternal mobility. Birth ball exercises may facilitate fetal descent, improve maternal pelvic mobility, and potentially shorten labor duration.

Intrapartum ultrasound has recently emerged as an objective method for assessing labor progress and fetal head position. Compared with digital vaginal examination, intrapartum ultrasound provides more reliable and reproducible measurements.

The aim of this study is to evaluate the effect of birth ball exercises performed during the active phase of labor on labor progress using intrapartum ultrasound. The findings of this study may contribute to understanding the potential benefits of birth ball exercises in supporting physiological labor.

Read the detailed description

This prospective interventional study aims to investigate the effect of birth ball exercises performed during the active phase of labor on labor progress using intrapartum ultrasound.

Participants will include pregnant women admitted to the labor ward who are in the active phase of labor and meet the study inclusion criteria. Participants will be divided into groups according to whether birth ball exercises are performed during the active phase of labor.

Intrapartum ultrasound will be used to evaluate parameters related to labor progress, including fetal head position and descent. Ultrasound measurements will be performed at predefined time points during the active phase of labor.

The primary objective of this study is to assess the effect of birth ball exercises on labor progress evaluated with intrapartum ultrasound. Secondary objectives include evaluating maternal comfort and changes in ultrasound parameters associated with fetal head progression during labor.

The results of this study may provide objective evidence regarding the role of birth ball exercises in supporting physiological labor and may contribute to improving non-pharmacological labor management strategies.

02

Conditions studied

  • Labor
  • Labor Progress

Keywords

  • Birth Ball
  • Intrapartum Ultrasound
  • Active Phase of Labor
  • Labor Progress
03

In context

Lead sponsor

Sakarya University is the lead sponsor of 183 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Pregnant women aged 18-35 years
  • Nulliparous women
  • Singleton pregnancy
  • Cephalic presentation
  • Gestational age between 38 and 40 weeks
  • Expected vaginal delivery
  • Cervical dilation ≥6 cm (active phase of labor)
  • Ability to perform birth ball exercises
  • Ability to provide informed consent

Exclusion criteria

Exclusion Criteria:

  • Multiple pregnancy
  • Non-cephalic presentation
  • Previous uterine surgery
  • Obstetric risk factors
  • Obstetric complications during labor (e.g., vaginal bleeding, fetal distress)
  • Gestational age \<37 weeks at admission
  • Alcohol or substance abuse
  • Inability to perform birth ball exercises
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
77 participants (actual)

Study arms

  • Experimental
    Birth Ball Exercise Group

    Pregnant women in the active phase of labor will perform birth ball exercises under supervision.

    Behavioral: Birth Ball Exercise

  • No intervention
    Control Group

    Participants will receive routine labor management without birth ball exercises.

Interventions

  • BehavioralBirth Ball Exercise

    Birth ball exercises performed during the active phase of labor to facilitate labor progress.

06

What researchers measure

Primary outcomes

  1. Angle of Progression (AoP) during the active phase of labor

    Angle of progression (AoP) was measured by transperineal intrapartum ultrasound. AoP was defined as the angle between the long axis of the pubic symphysis and a line drawn from the inferior edge of the pubic symphysis tangentially to the most distal point of the fetal skull. Measurements were obtained at 6 cm and 10 cm cervical dilation. AoP was expressed in degrees, with higher values indicating greater fetal head descent.

    Time frame: At 6 cm and 10 cm cervical dilation during the active phase of labor

  2. Head-Perineum Distance (HPD) during the active phase of labor

    Head-perineum distance (HPD) was measured by transperineal intrapartum ultrasound. HPD was defined as the shortest distance between the perineal skin surface and the outer bony limit of the fetal skull. Measurements were obtained at 6 cm and 10 cm cervical dilation. Lower HPD values indicate greater fetal head descent. HPD was expressed in centimeters.

    Time frame: At 6 cm and 10 cm cervical dilation during the active phase of labor

  3. Progression Distance (PD) during the active phase of labor

    Progression distance (PD) was measured by transperineal intrapartum ultrasound. PD was defined as the distance between the infrapubic line and the most distal point of the fetal skull. Measurements were obtained at 6 cm and 10 cm cervical dilation, and changes in PD reflected fetal head progression through the birth canal. PD was expressed in centimeters.

    Time frame: At 6 cm and 10 cm cervical dilation during the active phase of labor

  4. Fetal Head Direction (HD) during the active phase of labor

    Fetal head direction (HD) was assessed by transperineal intrapartum ultrasound according to the orientation of the fetal head within the maternal pelvis. Head direction was categorized as downward, horizontal, or upward. Assessments were performed at 6 cm and 10 cm cervical dilation. The outcome measure was reported categorically as downward, horizontal, or upward.

    Time frame: At 6 cm and 10 cm cervical dilation during the active phase of labor

  5. Fetal Head Position during the active phase of labor

    Fetal head position was assessed by intrapartum ultrasound according to the orientation of the fetal occiput within the maternal pelvis. Fetal head position was categorized as occiput anterior, occiput transverse, or occiput posterior. Assessments were performed at 6 cm and 10 cm cervical dilation. The outcome measure was reported categorically as occiput anterior, occiput transverse, or occiput posterior.

    Time frame: At 6 cm and 10 cm cervical dilation during the active phase of labor

Secondary outcomes

  1. Duration of the active phase of labor

    The time interval from the onset of the active phase of labor until full cervical dilation.

    Time frame: During labor

  2. Mode of delivery

    Type of delivery including spontaneous vaginal delivery, assisted vaginal delivery, or cesarean section.

    Time frame: At delivery

07

Study locations

1 site
  • (Sakarya Üniversitesi Eğitim ve Araştırma Hastanesi) Department of Obstetrics and Gynecology
    Sakarya, 54000, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07889700
Lead sponsor
Sakarya University
Responsible party
Sponsor
First posted
Oct 22, 2026
Start date
Nov 2, 2025
Primary completion
Jul 16, 2026
Completion
Sep 1, 2026
Last update
Oct 22, 2026

Study contacts

Hilal Uslu Yuvacı, MD
principal investigator · (Sakarya Üniversitesi Eğitim ve Araştırma Hastanesi) Department of Obstetrics and Gynecology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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