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Набор скоро начнётся NCT06999746

Device-Assisted Oropharyngeal Rehabilitation in Obstructive Sleep Apnea Patients Using Continuous Positive Airway Pressure

Без фазы С лечением Obstructive Sleep Apnea

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: Control, Oropharyngeal Exercise, Continuous positive airway pressure, Continuous positive airway pressure and oropharyngeal exercise.
Кому может быть актуально
Состояния в реестре: Obstructive Sleep Apnea. Базовые параметры: 20 лет — 68 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
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Effectiveness of Using Force Sensing Resistor to Assist Oropharyngeal Rehabilitation in Patients With Obstructive Sleep Apnea Using Continuous Positive Airway Pressure

Обзор

The goal of this clinical trial is to evaluate the effectiveness of device-assisted oropharyngeal rehabilitation (OPR) in improving upper airway muscle function and reducing obstructive sleep apnea (OSA) severity in adult patients diagnosed with OSA who are receiving continuous positive airway pressure (CPAP) therapy. The main questions it aims to answer are: 1. Does combining OPR with CPAP increase upper airway space volume compared to using CPAP alone? 2. Does OPR improve tongue muscle strength, and is this improvement associated with reduced CPAP pressure requirements? 3. Do patients receiving OPR (alone or combined with CPAP) show greater improvements in OSA severity and clinical symptoms compared to those receiving CPAP alone or no intervention? Researchers will compare four groups-Control, OPR-only, CPAP-only, and CPAP + OPR-to see if device-assisted OPR enhances treatment outcomes beyond CPAP alone. Participants will: 1. Be randomly assigned to one of four groups (Control, OPR-only, CPAP-only, CPAP+OPR). 2. Perform home-based OPR exercises (30-45 minutes/session, 1-2 sessions/day, 3-5 days/week for 3 months) in the OPR and CPAP+OPR groups. 3. Have their exercise monitored using a strength sensor, with intensity adjusted every 2-4 weeks during hospital visits. 4. Undergo assessments before and after the intervention, including: (1) Polysomnography for OSA severity, (2) CT and ultrasound for upper airway and tongue muscle structure, (3) Tongue muscle strength/endurance tests, (4) Sleep quality questionnaires, (5) CPAP usage and pressure reports.

Подробное описание

Background: Obstructive sleep apnea (OSA) is a common respiratory disorder associated with various complications, including cardiovascular, metabolic, and cognitive issues. Continuous positive airway pressure (CPAP) therapy can effectively reduce sleep apnea events and decrease the incidence of related complications. However, studies have shown that approximately half of OSA patients attempting CPAP therapy either cannot tolerate CPAP at all or only partially comply with it. Oropharyngeal rehabilitation (OPR), which involves isometric and isotonic exercises, can enhance the muscle tone of the tongue, pharynx, and soft palate. OPR may serve as one of the treatment options for OSA. Nevertheless, there is limited literature exploring the combined treatment approach of CPAP and OPR.

Methods:This study will recruit 30 200 adult OSA patients, who will be divided into two four groups: Control, OPR, CPAP alone and CPAP+OPR. The OPR training in OPR and CPAP+OPR groups will consist of home-based exercises performed for 30-45 minutes per session, once 1-2 session a day, five 3-5 days a week, over a period of three months. The training will be monitored using a strength sensor, and the intensity of the exercises will be adjusted every two weeks month during hospital visits. Both CPAP and CPAP+OPR groups will continue to wear CPAP every night, while the control group will receive monthly sleep hygiene education. The severity of OSA, upper airway space, tongue muscle length/thickness, tongue muscle strength/endurance, sleep quality, and CPAP usage report will be assessed using polysomnography, computed tomography scans, sonography, tongue muscle function tests, sleep quality questionnaires, and CPAP mask pressure at baseline and after three months of treatment.

Expected outcomes:

1. Compared to the group using only CPAP, the CPAP + OPR group will have an increased upper airway space volume after a 3-month follow-up. The upper airway space volume is negatively correlated with CPAP pressure and positively correlated with tongue muscle strength. 2. After 3 months of OPR treatment, the CPAP + OPR group will show an increase in tongue muscle strength, which is negatively correlated with CPAP pressure. 3. After 3 months of OPR treatment, both the OPR group and the CPAP+OPR group showed greater improvements in upper airway muscle function and greater reductions in obstructive sleep apnea severity and clinical symptoms compared to the control group and the CPAP group respectively.

Вмешательства

  • Другое Control
    Sleep hygiene education
  • Устройство Oropharyngeal Exercise
    Device-monitoring oropharyngeal exercise, 1-5 days a week for three months
  • Устройство Continuous positive airway pressure
    Continuous positive airway pressure, 1-5 days a week for three months
  • Устройство Continuous positive airway pressure and oropharyngeal exercise
    Continuous positive airway pressure and device-monitoring oropharyngeal exercise, 1-5 days a week for three months

Первичные конечные точки

  • Apnea-Hypopnea Index [Срок оценки: Baseline and 12 weeks post intervention]
Вторичные конечные точки (11)
  • Tongue Muscle Strength [Срок оценки: Baseline and 12 weeks post intervention]
  • Tongue Muscle Endurance [Срок оценки: Baseline and 12 weeks post intervention]
  • Pharyngeal Airway Volume [Срок оценки: Baseline and 12 weeks post intervention]
  • Cross Section Area on the Tip of Epiglottis [Срок оценки: Baseline and 12 weeks post intervention]
  • Anterior to Posterior Distance on the Tip of the Epiglottis [Срок оценки: Baseline and 12 weeks post intervention]
  • Lateral Distance on the Tip of Epiglottis [Срок оценки: Baseline and 12 weeks post intervention]
  • Sleep Quality [Срок оценки: Baseline and 12 weeks post intervention]
  • Daytime Sleepiness Level [Срок оценки: Baseline and 12 weeks post intervention]
  • Tongue Muscle Thickness [Срок оценки: Baseline and 12 weeks post intervention]
  • Median Pressure in Continuous Positive Airway Pressure [Срок оценки: 1-week average pre intervention, 1-week average post intervention and 1-month average during intervention for 3 months]
  • Median Usage Hours of Continuous Positive Airway Pressure [Срок оценки: 1-week average pre intervention, 1-week average post intervention and 1-month average during intervention for 3 months]

Критерии участия

Критерии включения

  • Adults aged 20 to 68 years
  • Newly diagnosed with mild to severe pure obstructive sleep apnea based on polysomnography

Критерии исключения

  • Severe allergic rhinitis
  • Sinusitis with nasal polyps
  • Adenoid hypertrophy
  • Bilateral tonsillar hypertrophy (Friedman grade ≥ III)
  • Lingual tonsil hypertrophy (Friedman grade ≥ III)
  • Body Mass Index (BMI) > 40
  • Alcohol or drug abuse within the past year
  • Pregnancy
  • Severe obstructive or restrictive pulmonary diseases
  • High-risk cardiovascular diseases during exercise (e.g., angina, myocardial infarction, heart failure, valvular heart disease)
  • History of central or peripheral neurological disorders that interfere with exercise prescription
  • Musculoskeletal or psychological disorders that interfere with exercise prescription
  • Other non-respiratory sleep disorders
  • Sleep disorders with concomitant central sleep apnea

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

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

Идентификаторы

NCT: NCT06999746 · B-BR-113-050

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗