Telerehabilitation in Patients With Bronchiectasis
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: telerehabilitation.
- Кому может быть актуально
- Состояния в реестре: Bronchiectasis, Telerehabilitation. 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
- Испания
- 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
Effectiveness of a 12-week Telerehabilitation Training in Patients With Bronchiectasis: A Randomized Controlled Trial.
Обзор
Background: Home-based telerehabilitation (TR) has demonstrated benefits comparable to conventional rehabilitation in patients with chronic obstructive pulmonary disease, asthma, and pulmonary fibrosis. However, TR has not been thoroughly investigated in patients with bronchiectasis, despite evidence suggesting improvements in exercise capacity and quality of life. Aims: To evaluate the effects of TR on functional capacity, quality of life, and inflammatory biomarkers, as well as its safety in patients with bronchiectasis. Study design: Single-center randomized controlled trial with a parallel-group design. Methods: Patients diagnosed with bronchiectasis will be recruited from the Surgical Medical Unit for Respiratory Diseases at Virgen del Rocío University Hospital. Participants will be randomly assigned to one of two groups: a control group receiving usual care, and a TR group undergoing supervised physical training for 12 weeks, three times per week. Outcome measures will include the 6-minute walk test, quality-of-life questionnaires, pulmonary function tests, symptom assessment, and adverse event recording, as well as sputum microbiology and analysis of inflammatory biomarkers. Assessments will be conducted at baseline and at the end of the intervention. Expected results: A 12-week TR program is expected to significantly improve exercise capacity and quality of life in the intervention group. Additionally, this study may contribute to the development of future clinical guidelines regarding the use of TR in patients with bronchiectasis.
Вмешательства
- Другое telerehabilitation
3 days per week: supervised resistance training that includes upper and lower limb and core exercises, initially using with low weights, performed in 2 sets with 10 repetitions, with progressive weekly increases depending on symptoms. 4 days per week: endurance training. Patients will walk on days when they do not perform strength training, for at least 30 minutes, with the duration gradually increased each month depending on their symptoms.
Первичные конечные точки
- 6-minute walk distance [Срок оценки: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
Вторичные конечные точки (12)
- The quality of life [Срок оценки: Baseline, after 12 weeks of telerehabilitation program and at 3 and 6 months after completing the telerehabilitation program.]
- Pulmonary function tests [Срок оценки: Baseline and after 12 weeks of telerehabilitation program.]
- Respiratory Muscle Strength [Срок оценки: Baseline and after 12 weeks of telerehabilitation program.]
- Exahled Nitric Oxide Fraction (FeNO) [Срок оценки: Baseline and after 12 weeks of telerehabilitation program.]
- Sputum microbiology [Срок оценки: Baseline, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
- Biological markers of Biological markers of inflammation [Срок оценки: Baseline and after 12 weeks of telerehabilitation program.]
- Dyspnoea [Срок оценки: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
- Bronchiectasis severity [Срок оценки: Baseline and after 12 weeks of telerehabilitation program.]
- Change from baseline in respiratory symptoms and adverse events. [Срок оценки: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
- Blood pressure [Срок оценки: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
- Heart rate [Срок оценки: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
- Oxygen saturation (SpO2) [Срок оценки: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.]
Критерии участия
Критерии включения
- Bronchiectasis diagnosed by high resolution computed tomography (HRCT) of the chest.
- Clinically stable patients (without hospitalizations, infection or changes in pharmacological treatment in the last month of the study beginning).
- Both gender
- Non smokers.
- Internet connection available.
Критерии исключения
- Inability to give informed consent to participate
- Less of 18 years
- With other lung related diseases (asthma, COPD and cystic fibrosis)
- Decompensated cardiovascular and metabolic diseases, neuromuscular or musculoskeletal that impede the realization of the protocol.
- Mental disorders that prevent the adequate participation in the tele-rehabilitation program.
- Simultaneous participation in another clinical trial.
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
Испания · 1 центр
- Hospital Universitario Virgen del Rocío — Seville
Идентификаторы
NCT: NCT07539571 · TRH-BQ