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NCT Number: NCT07659249

USE OF PERINEAL MIRROR DURING THE SECOND STAGE OF LABOR

Objective: This study was designed to evaluate the effect of perineal mirror use during the second stage of labor on the duration of the second stage, postpartum recovery, and perceived pain, support, and control levels during delivery.

Method: The study was designed as a randomized controlled experimental study to examine the effect of perineal mirror use on delivery outcomes in primiparous women. The study population consisted of primiparous pregnant women admitted to the maternity clinic between June 29, 2026, and October 30, 2026. The sample size was calculated using the G*Power 3.1.9.2 program with an effect size of 0.50, 5% Type I error, and 95% power level; a total of 72 participants were selected, 36 in the intervention group and 36 in the control group. Considering potential losses, the sample size was increased by 10%, and a total of 80 pregnant women were planned to be included in the study. Participants were randomly assigned to the intervention group using a perineal mirror and the control group receiving routine care. The following instruments will be used as data collection tools: Pregnancy Demographic Information Form, REEDA Scale, Visual Analog Scale (VAS), and Perceived Support and Control in Childbirth Scale.

Expected Outcome: It is predicted that the perineal mirror may increase the woman's active participation, motivation, and perceived control by allowing her to see the fetal descent and the progress of labor; consequently, it may reduce the duration of active pushing and the duration of the second stage. It is also thought that it may have positive effects on the birth experience, postpartum recovery, and perceived level of support and control. The research results are expected to provide evidence for non-invasive and low-cost applications that can be used in childbirth care.

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Key information

Age range

19 year–49 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women aged 19 and over
  • Women with term pregnancy (38+0 - 41+6)
  • Women with singleton pregnancy
  • Women who have had spontaneous vaginal delivery
  • Primiparous pregnant women
  • Women who voluntarily agree to participate in the study will be included.

Exclusion criteria

  • Women with high-risk pregnancies
  • Women with multiple pregnancies

Treatment and study plan

Perineal Mirror

Device

A perineal mirror will be positioned at the foot of the delivery bed during the active pushing phase of the second stage of labor. The mirror will allow the woman to visualize fetal descent and birth progress while continuing routine intrapartum care. The intervention is non-invasive, does not alter standard clinical management, and is intended to enhance maternal participation, motivation, perceived control, and support during childbirth.

Primary outcomes

  1. Duration of the Second Stage of Labor

    Time frame: During labor (second stage of labor)

    Duration of the second stage of labor, measured in minutes from complete cervical dilatation to birth.

Study contacts

Contact information is provided by the study sponsor or research team.

MELEK BALÇIK ÇOLAK, MSc, Assoc. Prof.

CONTACT

[email protected]

+90 264 295 3881

Sponsors and collaborators

Lead sponsor

Sakarya University

Other

Registry information

Official study title

THE EFFECT OF PERİNEAL MİRROR USE DURİNG THE SECOND STAGE OF LABOR ON THE DURATİON OF THE SECOND STAGE, RECOVERY, AND PERCEİVED PAİN, SUPPORT, AND CONTROL LEVELS DURİNG DELİVERY

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 22, 2026
Registry last updated
Jun 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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