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Набор скоро начнётся NCT06541717

Video Intervention Fertility Awareness Training

Без фазы С лечением Video-Based Fertility Awareness Training

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: Video-Based Fertility Awareness Training.
Кому может быть актуально
Состояния в реестре: Video-Based Fertility Awareness Training. Базовые параметры: от 18 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 →
Официальное название

Midwifery Students' Ovarian Reserve and Fertility Awareness: Effectiveness of Video Intervention

Обзор

This study was planned to evaluate the effects of video-based ovarian reserve awareness training applied to midwifery students on ovarian reserve, fertility awareness and anxiety of midwifery students. The research population will consist of second-year students studying in the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences University (SBU) in the fall semester of 2024-2025 academic year (N: 80). In this study planned as a semi-experimental pre-test and post-test design with a control group, in order to determine the sample size; the data were normally distributed, the standard deviation of the main mass was estimated as 1 and the effect size (effect size, difference) was estimated as 0.8. For the analysis to be conducted, it was calculated that the highest power value of the study would be 0.942182 if two independent n₁=40, n₂=40 samples were taken at a significance level of 5%. The G-power analysis result is given below. Students who volunteer to participate in the study will be assigned to the intervention and control groups with the computer-aided simple random sampling method. Computer-aided randomization will be used in the study, and the number of cases will be entered through the program with the URL address https://www.randomizer.org and random assignment will be made to the intervention and control groups. The study will be conducted single-blind. Midwifery students in the intervention group of the study will be given video-based ovarian reserve and fertility awareness training. A pre-training information meeting will be held with midwifery students who volunteered to participate in the study and were assigned to the intervention group. The midwifery students will be administered the "Ovarian Reserve Information Form", "Fertility Awareness Scale" and "State Anxiety Scale" before and after the training.

Вмешательства

  • Другое Video-Based Fertility Awareness Training
    Students will be shown 3 15-minute videos created by researchers on the anatomy and physiology of the male and female reproductive systems, the physiology of pregnancy, fertility awareness development and its importance in terms of infertility.

Первичные конечные точки

  • Introductory Information Form [Срок оценки: 10 minutes]
  • Ovarian Reserve Information Form [Срок оценки: 10 minutes]
  • Fertility Awareness Scale (FAS) [Срок оценки: 10 minutes]
  • State-Trait Anxiety Inventory [Срок оценки: 10 minutes]
Вторичные конечные точки (3)
  • Ovarian Reserve Information Form [Срок оценки: 10 minutes]
  • Fertility Awareness Scale (FAS) [Срок оценки: 10 minutes]
  • State-Trait Anxiety Inventory [Срок оценки: 10 minutes]

Критерии участия

Критерии включения

  • To be a volunteer to participate in the research.
  • To be an active student in the 2nd year of the Midwifery Department of Hamidiye Health Sciences Faculty, University of Health Sciences.

Критерии исключения

  • Being a passive student in the 2nd year of the Midwifery Department of Hamidiye Health Sciences Faculty, University of Health Sciences.

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
Простое слепое
Основная цель
Другое

Центры проведения

Turkey (Türkiye) · 1 центр
  • University of Health Sciences — Istanbul

Идентификаторы

NCT: NCT06541717 · SBÜ-AYDINKARTAL-008

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗