- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07566026
Breathing Exercises During Labor and Maternal Outcomes
Effects of Breathing Exercises During Labor on Maternal Stress, Satisfaction, and Birth Outcomes: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Labor is a physiological process that may be accompanied by pain, anxiety, and psychological stress, which can negatively affect birth satisfaction and labor outcomes. Non-pharmacological interventions such as breathing exercises are widely used to support women during labor.
In this randomized controlled experimental study, pregnant women admitted to the labor and delivery unit during the latent phase were randomly assigned to either an experimental group receiving guided breathing exercises throughout labor or a control group receiving routine intrapartum care only. Breathing exercises were applied continuously during uterine contractions until full cervical dilatation.
Maternal pain intensity, anxiety, traumatic birth perception, birth satisfaction, and labor outcomes including labor duration and obstetric interventions were assessed using validated measurement tools. The study aimed to determine whether breathing exercises could improve maternal psychological well-being, enhance birth satisfaction, and positively influence labor outcomes.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey (Türkiye)
- Nilgün Avcı
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Pregnant women admitted to the labor and delivery unit during the latent phase
- Women planning vaginal birth
- Volunteered to participate
Exclusion Criteria:
- Women who did not speak Turkish
- Women with auditory or mental health problems
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Breathing Exercise Group
Participants received guided breathing exercises throughout labor in addition to routine intrapartum care.
|
Pregnant women were instructed and guided to perform slow, controlled breathing exercises during each uterine contraction from the latent phase until full cervical dilatation.
|
|
No Intervention: Routine Care Group
Participants received routine intrapartum care only.
No breathing exercises were applied.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Birth Satisfaction
Time Frame: During the fourth stage of labor (within 2 hours after birth).
|
Birth satisfaction assessed using the Short Form of the Birth Satisfaction Scale (BSS-R). Scores range from 0 to 40; higher scores indicate greater satisfaction. |
During the fourth stage of labor (within 2 hours after birth).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Labor Pain Intensity
Time Frame: Repeatedly during labor from admission to the labor unit until delivery.
|
Pain intensity measured using the Visual Analog Scale (VAS).
Scores range from 0 to 10; higher scores indicate more severe pain.
|
Repeatedly during labor from admission to the labor unit until delivery.
|
|
Labor-Related Anxiety
Time Frame: During the fourth stage of labor (within 2 hours after birth).
|
Anxiety measured using the Oxford Worries About Labour Scale.
Scores range from 10 to 40; higher scores indicate greater anxiety.
|
During the fourth stage of labor (within 2 hours after birth).
|
|
Traumatic Birth Perception
Time Frame: At admission to the labor unit (baseline) and during the fourth stage of labor (within 2 hours after birth).
|
Traumatic birth perception measured using the Traumatic Birth Perception Scale.
Scores range from 0 to 130; higher scores indicate greater traumatic perception.
|
At admission to the labor unit (baseline) and during the fourth stage of labor (within 2 hours after birth).
|
|
Fetal Heart Rate During NST
Time Frame: During the NST monitoring session (approximately 20 minutes, same visit).
|
Fetal heart rate assessed from NST recordings during the monitoring session.
Measured in beats per minute; normal patterns indicate better fetal well-being.
|
During the NST monitoring session (approximately 20 minutes, same visit).
|
|
Fetal Movement Count During NST
Time Frame: During the NST monitoring session (approximately 20 minutes, same visit).
|
Number of fetal movements recorded by the mother using the event marker during NST monitoring. Higher counts indicate greater fetal activity. |
During the NST monitoring session (approximately 20 minutes, same visit).
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Effects of Breathing Exercises
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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