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Набор скоро начнётся NCT07674108

VR Simulation-Based Implanted Port Catheter Training in Nursing Students

Без фазы С лечением Nursing Education Clinical Competence

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: Virtual Reality Simulation-Based Implanted Port Catheter Training.
Кому может быть актуально
Состояния в реестре: Nursing Education, Clinical Competence. Базовые параметры: от 18 лет · Все.
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

Effectiveness of Virtual Reality Simulation-Based Implanted Port Catheter Training on Knowledge, Learning Satisfaction and Motivation in Nursing Students: A Randomized Controlled Trial

Обзор

Implanted port catheter care is a critical clinical skill in oncology nursing, requiring accurate knowledge, aseptic technique, safe procedural practice, and early recognition of potential complications. This parallel group randomized controlled study aims to evaluate the effectiveness of virtual reality simulation-based implanted port catheter training in undergraduate nursing students. Eligible second-year nursing students will be randomly assigned to either an intervention group or a control group. All students will receive a two-hour traditional implanted port catheter training session in the classroom setting. In addition to traditional training, students in the intervention group will receive virtual reality simulation-based training consisting of two scenarios: safe implanted port catheter access and extravasation/complication management. The control group will receive only traditional training.

Вмешательства

  • Поведенческое Virtual Reality Simulation-Based Implanted Port Catheter Training
    The virtual reality simulation-based implanted port catheter training will be provided in addition to traditional classroom-based training. The VR training will be delivered individually using a Meta Quest 3 headset and will consist of two structured scenarios. The first scenario will focus on safe implanted port catheter access, line verification, flushing, dressing, and documentation. The second scenario will focus on recognition and management of suspected extravasation or related complicatio

Первичные конечные точки

  • Change in Implanted Port Catheter Knowledge Assessment Checklist Score [Срок оценки: Baseline, pre-intervention; immediately after the intervention]
  • Change in Student Satisfaction and Self-Confidence in Learning Scale Score [Срок оценки: Baseline, pre-intervention; immediately after the intervention]
  • Change in Instructional Materials Motivation Survey Score [Срок оценки: Baseline, pre-intervention; immediately after the intervention]
Вторичные конечные точки (1)
  • Implanted Port Catheter Application Performance Score [Срок оценки: During the virtual reality simulation session, immediately after completion of each VR scenario]

Критерии участия

Критерии включения

  • Being 18 years of age or older
  • Being an undergraduate nursing student
  • Having completed the Internal Medicine Nursing course
  • Voluntarily agreeing to participate in the study
  • Providing written informed consent

Критерии исключения

  • Having any communication barrier that may prevent participation in the study or completion of the study forms
  • Having neck pain or neck injury severe enough to prevent head movement
  • Having a visual problem that prevents safe use of the virtual reality application
  • Experiencing severe nausea or dizziness during the virtual reality application
  • Having a diagnosed history of epilepsy

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
  • Izmir Bakircay University — Izmir

Идентификаторы

NCT: NCT07674108 · 2026/2823

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗