NCT07446699

Brief Summary

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

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
128

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 18, 2026

Completed
11 days until next milestone

Study Start

First participant enrolled

March 1, 2026

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 3, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Completed
Last Updated

April 8, 2026

Status Verified

February 1, 2026

Enrollment Period

5 months

First QC Date

February 18, 2026

Last Update Submit

April 2, 2026

Conditions

Keywords

duration of laborpainpushingfatigue

Outcome Measures

Primary Outcomes (2)

  • Visual Analogue Scale

    It is used to assess pain intensity. The scale is graded from 0 to 10 cm in length, where 0 represents no pain and 10 represents the most severe pain. It is applied by having the individual mark a point corresponding to the intensity of the pain they feel. The distance between the marked point and the lowest end of the line is measured in centimeters, and the resulting numerical value indicates the patient's pain intensity.

    Baseline

  • Visual Similarity Scale for Fatigue

    The Visual Analogy Scale for Fatigue consists of 18 items. 13 items form the fatigue subscale, and five items form the energy subscale. The most positive and the most negative statements are located at opposite ends of the scale, and horizontal lines with 10 cm intervals are placed between the two statements. A high score on the fatigue subscale and a low score on the energy subscale indicate a higher intensity of fatigue. The minimum score for the fatigue subscale was 0, and the maximum score was 130; the minimum score for the energy subscale was 0, and the maximum score was 50.

    Baseline

Secondary Outcomes (2)

  • Visual Analogue Scale

    In the fourth stage of labor

  • Visual Analogy Scale for Fatigue

    In the fourth stage of labor

Study Arms (2)

Spontaneous pushing group

EXPERIMENTAL

This is the type of pushing that a pregnant woman does by making sounds and exhaling. The pregnant woman pushes spontaneously, and the intensity of the push is consistent with the contractions. Although contractions occur during spontaneous pushing, the pregnant woman does not push until she feels the urge to push. Pushing occurs with the urge to push. The pregnant woman begins to push with her resting breath.

Behavioral: Spontaneous straining

Valsalva straining group

EXPERIMENTAL

This is the type of pushing performed by the pregnant woman while holding her breath. This type of pushing is generally considered by healthcare professionals as directed pushing. The researcher will guide the woman on when and how to push.

Behavioral: Valsalva type pushing

Interventions

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.

Spontaneous pushing group

* 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.

Valsalva straining group

Eligibility Criteria

Age19 Years - 35 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sivas Cumhuriyet University

Sivas, 58140, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Labor PainPainFatigue

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Sukran Ertekin Pinar, Prof. Dr.

    Cumhuriyet University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr.

Study Record Dates

First Submitted

February 18, 2026

First Posted

March 3, 2026

Study Start

March 1, 2026

Primary Completion

July 30, 2026

Study Completion

July 30, 2026

Last Updated

April 8, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

There is not a plan to make IPD available.

Locations