Меню
Набор скоро начнётся NCT07659249

USE OF PERINEAL MIRROR DURING THE SECOND STAGE OF LABOR

Без фазы С лечением Labor, Second Stage Vaginal Delivery Primiparity Perineal Mirror Use

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Perineal Mirror.
Кому может быть актуально
Состояния в реестре: Labor, Second Stage, Vaginal Delivery, Primiparity, Perineal Mirror Use. Базовые параметры: 19 лет — 49 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Turkey (Türkiye)
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Не всё понятно в терминах? Прочитайте наш гид для пациентов →

Официальное название

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

Обзор

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.

Вмешательства

  • Устройство Perineal Mirror
    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.

Первичные конечные точки

  • Duration of the Second Stage of Labor [Срок оценки: During labor (second stage of labor)]

Критерии участия

Критерии включения

  • 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.

Критерии исключения

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

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Поддерживающая терапия

Центры проведения

Turkey (Türkiye) · 1 центр
  • Düzce Atatürk State Hospital — Düzce

Идентификаторы

NCT: NCT07659249 · E-43012747-050.04-579687-319

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗