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Clinical Trials in Turkey / NCT07446699
Active, not recruiting Not applicable

The Effect of Pushing Techniques Used During Childbirth on Women's Labor Duration, Pain, and Fatigue Levels

NCT07446699 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-01
Last updated
2026-04-08

Condition(s) studied

ChildbirthDuration of LaborLabor PainsPushing During ChildbirthFatigue During Childbirth

Investigational drug(s) / intervention(s)

Spontaneous strainingValsalva type pushing

Spontaneous straining: In this pushing method, pregnant women remain in a squatting position during the second stage of labor. The researcher provides the women with information about spontaneous pushing. The women will be supported in spontaneous pushing, and their urge to push will be taken into consideration. In spontaneous pushing: Regular breathing until the urge to push is felt when contractions begin, inhaling and contracting the core muscles, pushing slowly, exhaling smoothly while contracting during pushing, pushing for 5-6 seconds while exhaling, pushing smoothly and regularly for 5-6 seconds while inhaling and exhaling, and regular breathing when contractions slow down.

Valsalva type pushing: * When contractions begin, take two regular breaths, * Then take a deep breath and hold it, * Tighten your diaphragm and abdominal muscles, * Push as hard and for as long as possible (10-15 seconds), * Continue holding your breath while pushing (glottis closed), * Exhale, take a deep breath, continue holding your breath, * Push hard again for 10-15 seconds, * Stop pushing when contractions ease, * Relax and try to rest until the next contraction.

Study summary

The Effect of Pushing Techniques Used During Childbirth on Women's Labor Duration, Pain, and Fatigue Levels

Eligibility

Sex
FEMALE
Min age
19 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Being between 19-35 years old * Having had a normal vaginal delivery, * Being between 38-41 weeks pregnant, * Having a cervical dilation of 8 cm or more, * Being nulliparous, * Having a singleton pregnancy, * Not having a diagnosed physical health problem in the fetus or mother, * Not having a diagnosed mental health problem in the mother, * Not having hearing or perception problems, * Volunteering to participate in the study. Exclusion Criteria: * Being under 19 or over 35 years of age, * Having undergone a planned cesarean section, * Being gestational age between 38 and 41 weeks, * Cervical dilation less than 8 cm, * Being multiparous, * Having a multiple pregnancy, * Having a diagnosed physical health problem in the fetus or mother, * Having a diagnosed mental health problem in the mother, * Having hearing and perception problems, * Not being a volunteer to participate in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sivas Cumhuriyet University Sivas Turkey (Türkiye)

More Cumhuriyet University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07446699 on ClinicalTrials.gov ↗ ← All trials in Turkey