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Набор скоро начнётся NCT07078656

Effect of Video Training on Patients' Self-Efficacy After Colorectal Surgery

Без фазы С лечением Colorectal Cancer

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: Postoperative management.
Кому может быть актуально
Состояния в реестре: Colorectal Cancer. Базовые параметры: 18 лет — 65 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 →

Обзор

The purpose of the study is to determine the effect of virtual reality video training on the self-efficacy of patients after colorectal surgery. Thus, correct planning can be provided for trainings that will provide information to patients according to their needs during the nursing care process. Does virtual reality video training have an effect on participants' perceptions of self-efficacy after colorectal surgery? The researchers will conduct the self-efficacy survey on another group of participants without repeating the training to see the impact of the training. Participants in the experimental group will receive training on the second postoperative day and they will apply a self-efficacy survey on the tenth day after discharge. Participants in the control group will not receive training on the second postoperative day. They will complete a self-efficacy survey on the tenth day after discharge.

Подробное описание

The data obtained in the study will be evaluated in a computer environment using the IBM SPSS Version 22.0 package program. The conformity of the data to normal distribution will be assessed using the Kolmogorov-Smirnov test, and if the p value is p\<0.05, Skewness and Kurtosis values will be examined. Descriptive statistics will be applied to sociodemographic variables. For intergroup comparisons of pre-test and post-test measurements of the experimental and control groups according to dependent variables, the significance test for the difference between two independent means will be used; for non-parametric data, the Mann Whitney U test will be used. For comparisons of pre-test and post-test measurements within the experimental and control groups according to dependent variables, the t-test for dependent groups will be used; for non-parametric data, the Wilcoxon test will be used. The results will be evaluated at a 95% confidence interval and a significance level of p\<0.05.

Вмешательства

  • Поведенческое Postoperative management
    The patients who agreed to participate in the study will be asked to fill out a "Patient Introduction Form" by the researchers after obtaining permission from the experimental group with the "Informed Consent Form" the day before the surgery. On the 2nd day after laparoscopic colorectal surgery, virtual reality glasses will be worn by the patients and they will watch a 10-minute training video on the care of the patient after colorectal surgery. The training content will consist of topics such a

Первичные конечные точки

  • Self-Efficacy Scale in Colorectal Cancer Surgery [Срок оценки: one week after registration up to 3 months]

Критерии участия

IInclusion Criteria:

  • aged 18 and over
  • aged 65 and under
  • undergoing laparoscopic general surgery under general anesthesia
  • with no vision, hearing, or perception problems
  • with no communication problems
  • without nausea, vomiting, dizziness, etc.
  • with an ASA score of I, II, or III
  • who voluntarily agreed to participate in the study

Критерии исключения

  • who have not undergone laparoscopic surgery
  • who are hemodynamically unstable
  • with an ASA score of IV
  • with neurological or psychological problems
  • Emergency and unplanned cases

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Поддерживающая терапия

Центры проведения

Turkey (Türkiye) · 1 центр
  • Etlik City Hospital — Ankara

Идентификаторы

NCT: NCT07078656 · AnkaraYBU-SBF-GG-01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗