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Идёт набор NCT07090200

Rehabilitation Intervention for COPD Combined With Cardiovascular and Cerebrovascular Diseases

Без фазы С лечением Respiratory Diseases Cardiovascular Diseases Cerebrovascular Diseases

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: Pulmonary Rehabilitation Care Group, The Routine Care (Non-Pharmacological and Pharmacological Treatments ) Group.
Кому может быть актуально
Состояния в реестре: Respiratory Diseases, Cardiovascular Diseases, Cerebrovascular Diseases. 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
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Обзор

Firstly, to screen out the high-risk population of COPD combined with cardiovascular and cerebrovascular diseases, COPD with cardiovascular and make a diagnosis. Then, to evaluate the therapeutic effect of Pulmonary rehabilitation exercise and usual care for three months. And finally, to build a trinity model of rehabilitation management of COPD patients. The objective of this project is to establish and promote the application of diagnostic and treatment norms.

Подробное описание

Firstly, to screen out the high-risk population of COPD combined with cardiovascular and cerebrovascular diseases, COPD with cardiovascular and make a diagnosis. Then, participants were randomized (1:1) to either the optimized or routine group via a computer-generated random number table. The Routine Care Group received treatment for three months and follow-up with medications prescribed according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2025 Report. The Pulmonary Rehabilitation Care Group received the Pulmonary rehabilitation exercise and usual care for three months. Next, Observe the changes in the improvement of acute exacerbation frequency (times/year/person)，CAT Scoring and St. George's Respiratory Questionnaire (SGRQ), as well as lung ventilation and diffusion function of the two groups of patients one year after the intervention. And finally, to build a trinity model of rehabilitation management of COPD patients.

Вмешательства

  • Комбинированный продукт Pulmonary Rehabilitation Care Group
    participants were randomized (1:1) to either the optimized or routine group via a computer-generated random number table. The Routine Care Group received treatment for three months and follow-up with medications prescribed according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2025 Report. The Pulmonary Rehabilitation Care Group received the Pulmonary rehabilitation exercise and usual care for three months. Next, Observe the changes in the improvement of acute exacerbatio
  • Другое The Routine Care (Non-Pharmacological and Pharmacological Treatments ) Group
    participants were randomized (1:1) to either the optimized or routine group via a computer-generated random number table. The Routine Care Group received treatment for three months and follow-up with medications prescribed according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2025 Report. Next, Observe the changes in the improvement of acute exacerbation frequency (times/year/person)，CAT Scoring and St. George's Respiratory Questionnaire (SGRQ), as well as lung ventilati

Первичные конечные точки

  • The proportion of high-risk and diagnosed individuals with COPD [Срок оценки: through study completion, an average of 4 year]
  • the improvement of acute exacerbation frequency (times/year/person) [Срок оценки: through study completion, an average of 4 year]
Вторичные конечные точки (3)
  • Blood pressure [Срок оценки: through study completion, an average of 4 year]
  • blood lipids [Срок оценки: through study completion, an average of 4 year]
  • FBG(fasting blood-glucose) [Срок оценки: through study completion, an average of 4 year]

Критерии участия

Критерии включения

  • Committed to adhering to the study protocol and cooperating with the implementation of the entire research process.
  • Aged 18 years or older, regardless of gender.
  • Signed informed consent form.

Критерии исключения

  • Individuals with severe mental illness.
  • Individuals assessed by medical personnel as having a disease that requires immediate hospitalization or a severe, uncontrollable condition that is life-threatening in the short term.
  • Women who are pregnant, breastfeeding, or using inappropriate contraception methods.
  • Individuals who refuse to cooperate with follow-up questionnaires or specimen collection.
  • Patients currently participating in other interventional clinical drug trials.

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Другое

Центры проведения

Китай · 1 центр
  • Union hospital, Tongji Medical college, Huazhong University of Science and Technology — Ухань

Идентификаторы

NCT: NCT07090200 · XHJY-Chronic disease · 2023ZD0509905

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗