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Идёт набор NCT05739617

Comprehensive Respiratory Training Exercise Program in Obstructive Sleep Apnea

Без фазы С лечением Obstructive Sleep Apnea of Adult

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: Comprehensive Respiratory Training Exercise Program, Sleep hygiene education.
Кому может быть актуально
Состояния в реестре: Obstructive Sleep Apnea of Adult. Базовые параметры: 20 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
Тайвань
Следующий шаг
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Официальное название

Combining Sonography to Explore the Therapeutic Effect and Mechanism of a Comprehensive Respiratory Training Exercise Program on Cardiorespiratory Endurance and Airway Muscle Function in Obstructive Sleep Apnea

Обзор

Obstructive sleep apnea (OSA) is a multi-factorial sleep disorder. Complete collapse or partial collapse in the airway increases the risk of developing cardiovascular and kidney-related disease in OSA patients. Resulting in an increase in medical expenses and workload for the healthcare worker. Multilevel of upper airway muscles especially the genioglossus muscle showed to contribute to airway obstruction as it fatigues easily. The endurance level of OSA patients was shown to be significantly lower. Therefore, the goal of this experimental study is to assess the feasibility and effectiveness of a comprehensive respiratory training exercise program on cardiorespiratory endurance, airway muscle function, and sleep parameters in patients with obstructive sleep apnea (OSA). Aside from exploring the therapeutic effect, the results of the study will be used to explore the mechanism of the treatment in relation to the changes in the OSA severity.

Подробное описание

Newly diagnosed OSA subjects, aged 20-65 years old, and with body mass index between 18-30 kg.m-2 will be recruited. The participants will be randomly divided into the control group (sleep hygiene education) and the intervention group (comprehensive respiratory training exercise program). Participants from the intervention group will undergo 3 months of a comprehensive respiratory training exercise program while the control group will be provided sleep hygiene education. Polysomnography (PSG), cardiopulmonary exercise testing, sonography (during the awake stage, functional tasks, Müller's maneuver, and natural sleep), tongue strength and tongue endurance assessment, jaw strength measurement, Computed Tomography (CT), Drug-Induced Sleep Endoscopy (DISE), respiratory muscle strength, pulmonary function test, and sleep quality questionnaires will be collected before and after 3 months of intervention.

Expected contribution to clinical medicine

* The feasibility of this comprehensive respiratory training exercise program in improving cardiorespiratory endurance, leading to an increase in the survival rate and reduced risk of cardiovascular disease of OSA patients. * Based on the ultrasound's findings in the awake stage (normal breathing, functional tasks, and Müller's maneuver) and overnight sleep, allow a better understanding of the effects of these exercises on the changes of tongue and oropharyngeal structures during the static and dynamic stages. * The practicability of the ultrasound assessment in the clinical setting on OSA patients is to identify the changes in the tongue and oropharyngeal structures. Based on ultrasound image capture, it provides individualized and precise training by modifying the training and providing feedback to OSA patients during their exercise training.

Вмешательства

  • Другое Comprehensive Respiratory Training Exercise Program
    This comprehensive respiratory training exercise program consists of four main components, including oropharyngeal muscle training, respiratory muscle training, aerobic exercise, and sleep hygiene education.
  • Другое Sleep hygiene education
    Sleep hygiene education

Первичные конечные точки

  • Change in Apnea-Hypopnea Index (AHI) [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Oxygen Desaturation Index (ODI) [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Maximum Oxygen Consumption (Vo2max) [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Tongue Muscle Thickness [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Tongue Muscle Stiffness [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Tongue Muscle Strength [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Tongue Muscle Endurance [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Jaw strength [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Pharyngeal Airway Volume [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Cross Section Area on the Tip of Epiglottis [Срок оценки: Baseline to 3 months (post-training)]
Вторичные конечные точки (4)
  • Change in Maximal Inspiratory Pressure (PImax) [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Maximal Expiratory Pressure (PEmax) [Срок оценки: Baseline to 3 months (post-training)]
  • Change in forced vital capacity (FVC) % predicted [Срок оценки: Baseline to 3 months (post-training)]
  • Change in Forced Expiratory Volume in one second (FEV1)/ forced vital capacity(FVC) % [Срок оценки: Baseline to 3 months (post-training)]

Критерии участия

Критерии включения

  • Newly diagnosed with OSA (AHI≥ 5 events per hour)
  • Age between 20 to 65 years old
  • BMI of 18-30 kg.m-2

Exclusion Criteria: Diagnosed with any of the following diseases below:

  • Central or mixed types of sleep apnea
  • Neuromuscular disease
  • Severe cardiovascular disease
  • Active psychiatric disease
  • Head or neck disease or cancer
  • Structural abnormalities over the upper respiratory airway
  • Performed any operation or treatment over the neck before
  • Pregnancy

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
Лечение

Центры проведения

Тайвань · 1 центр
  • National Cheng Kung University Hospital — Tainan

Идентификаторы

NCT: NCT05739617 · A-BR-111-079

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗