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Набор скоро начнётся NCT06813144

Effectiveness of Respiratory Muscle Training with a Mobile Application After Lobectomy

Без фазы С лечением Video Assisted Thoracic Surgery (VATS) Thoracic Surgery Respiratory Muscle Lung Cancer (NSCLC)

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: inspiratory muscle exercise.
Кому может быть актуально
Состояния в реестре: Video Assisted Thoracic Surgery (VATS), Thoracic Surgery, Respiratory Muscle, Lung Cancer (NSCLC). 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 →

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Официальное название

Evaluation of the Effectiveness of Respiratory Muscle Training with a Mobile Application in the Early Postoperative Period After Lobectomy

Обзор

It has been observed that there are negative effects on respiratory muscle strength following lobectomy. This has led to the necessity of respiratory muscle training to mitigate these adverse effects. Most studies conducted so far focus on the late postoperative period, and there are only a few studies evaluating the effectiveness of early postoperative inspiratory muscle training (IMT). It is believed that this method could be useful for facilitating patient follow-up and increasing patient motivation through visual feedback.

Подробное описание

It has been observed that there are negative effects on respiratory muscle strength following lobectomy. This has led to the necessity of respiratory muscle training to mitigate these adverse effects. Most studies conducted so far focus on the late postoperative period, and there are only a few studies evaluating the effectiveness of early postoperative inspiratory muscle training (IMT). Additionally, there is currently no study assessing the effectiveness of IMT using a smart adapter in patients who have undergone lobectomy. It is believed that this method could be useful for facilitating patient follow-up and increasing patient motivation through visual feedback. The aim of this study is to examine the changes in respiratory muscle strength and exercise capacity in patients after lobectomy via VATS, comparing classical IMT, mobile application-supported IMT, and a control group that does not receive IMT.

Вмешательства

  • Другое inspiratory muscle exercise
    Inspiratory muscle training will be given with or without smart adaptor.

Первичные конечные точки

  • Inspiratory muscle strength [Срок оценки: Measurements will be performed before surgery (the day before surgery), at discharge and during the follow-up period after surgery (10-15 days after discharge).]
  • Expiratory muscle strength [Срок оценки: Measurements will be performed before surgery (the day before surgery), at discharge and during the follow-up period after surgery (10-15 days after discharge).]
Вторичные конечные точки (6)
  • Functional exercise capacity [Срок оценки: Evaluations will be made before surgery (the day before surgery) and during the follow-up period (10-15 days after discharge).]
  • Postoperative Pulmonary Complications [Срок оценки: Postoperative first-fifth days.]
  • Exercise Motivation [Срок оценки: The evaluation will be made during the control period (10-15 days after discharge).]
  • Dyspnea Level [Срок оценки: An evaluation will be made in the preoperative (the day before surgery) and control period (10-15 days after discharge).]
  • Quality of Life [Срок оценки: The evaluation will be made during the preoerative (the day before surgery) and control (10-15 days after discharge) period.]
  • Physical Performance [Срок оценки: Evaluations will be made in the preoperative (the day before surgery) and control (10-15 days after discharge) periods.]

Критерии участия

Критерии включения

  • Volunteering to participate in the study,
  • Being clinically stable,
  • Being a lung cancer patient with a planned lobectomy with VATS,
  • Being between the ages of 18-65,
  • Being able to cooperate with the tests to be performed.

Критерии исключения

  • Having any orthopedic or neurological problem that prevents walking,
  • Having undergone any surgery related to the thoracic wall,
  • Having diseases that will affect respiratory parameters such as severe heart failure, severe chronic obstructive pulmonary disease (COPD).

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
Двойное слепое
Основная цель
Лечение

Центры проведения

Turkey (Türkiye) · 1 центр
  • Hacettepe University — Ankara

Идентификаторы

NCT: NCT06813144 · E-30603717-050.04-2400055696

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗