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Breathing Exercises Guided by Student Midwives During Labor

The Effect of Breathing Exercises Applied Under the Guidance of Student Midwives During Birth on Labor Pain, Labor Duration and Birth Satisfaction: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07357246
Acronym
BREATH
Enrollment
90
Registered
2026-01-21
Start date
2024-09-01
Completion date
2025-03-15
Last updated
2026-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childbirth, Labor Pain and to Reduce Pain, Normal Labor

Keywords

Breathing Exercises, Labor Pain, Student Midwives, Birth Satisfaction, Labor Duration, Midwifery Care

Brief summary

This randomized controlled trial aimed to evaluate the effect of breathing exercises applied under the guidance of student midwives during labor on labor pain, labor duration, and birth satisfaction. The intervention group received structured breathing exercises guided by student midwives throughout labor, while the control group received routine intrapartum care. Outcomes were assessed during labor and in the early postpartum period

Detailed description

This study is designed to evaluate the effect of a midwifery-led intervention on labor pain intensity and birth satisfaction among women giving birth vaginally. The study will be conducted as a controlled clinical study in a maternity hospital setting. Eligible pregnant women who are admitted to the labor ward and meet the inclusion criteria will be invited to participate and will provide informed consent prior to enrollment. The study aims to determine whether the midwifery-led intervention is associated with reduced labor pain intensity and improved birth satisfaction compared to routine care.

Interventions

Structured breathing exercises delivered and monitored by student midwives during labor.

Standard intrapartum care provided according to hospital protocols.

Sponsors

Antalya Bilim University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women aged 18 years and older Term pregnancy (≥37 weeks of gestation) Singleton pregnancy Planning vaginal birth In the active phase of labor Able to communicate and provide informed consent

Exclusion criteria

* High-risk pregnancy (e.g., preeclampsia, placenta previa, severe medical complications) Multiple pregnancy Planned cesarean section Use of pharmacological pain relief at admission (e.g., epidural analgesia) Known fetal anomalies Inability to participate in breathing exercises

Design outcomes

Primary

MeasureTime frameDescription
Labor pain intensity measured by the Visual Analog Scale (VAS) (0-10)At admission to the labor ward (baseline) and at cervical dilatation of 6-7 cm.Labor pain intensity will be assessed using a 10-cm Visual Analog Scale (VAS), where 0 indicates "no pain" and 10 indicates "worst pain imaginable." The outcome will be the VAS score reported by the participant at each assessment time point.

Secondary

MeasureTime frameDescription
Birth satisfaction measured by the Birth Satisfaction Scale Revised (BSS-R)Within the first 24 hours postpartumBirth satisfaction will be assessed using the Birth Satisfaction Scale-Revised (BSS-R), a 10-item scale with total scores ranging from 0 to 40, where higher scores indicate greater birth satisfaction.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSeda Serhatlioglu, Doctorate

Antalya Bilim Üniversitesi

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026