- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07718009
Effects of Alternating Altitude Training Versus Fixed-Altitude Training on Exercise Capacity and Physiological Adaptations in Elite Race Walkers: A Randomized Controlled Trial
Effects of Alternating Altitude Training Versus Fixed-Altitude Training on Physical Performance and Physiological Adaptations in Elite Race Walkers: A Randomized Controlled Trial
Обзор исследования
Статус
Условия
Вмешательство/лечение
Тип исследования
Регистрация (Оцененный)
Фаза
- Непригодный
Контакты и местонахождение
Контакты исследования
- Имя: Binghong Gao
- Номер телефона: +853 8591 2000
- Электронная почта: research_ethics@ipm.edu.mo
Места учебы
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Macao, Китай
- Рекрутинг
- Macao Polytechnic University, Faculty of Health Sciences and Sports, Macao, China
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Контакт:
- Chaoran Han
- Номер телефона: +853 8591 2000
- Электронная почта: hanchaoran1999@outlook.com
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
Принимает здоровых добровольцев
Описание
Inclusion Criteria:
- Male and female elite race walkers aged 16-26 years. Registered athletes from the Yunnan Provincial Race Walking Team. Long-term residents of high-altitude regions with regular altitude training experience.
Healthy and medically cleared to participate in high-intensity training and hypoxic exposure.
Able to complete the prescribed training program and all outcome assessments. Provided written informed consent before enrollment. For participants younger than 18 years, written informed consent will also be obtained from a parent or legal guardian.
Exclusion Criteria:
- Any cardiovascular, respiratory, metabolic, neurological, or other medical condition contraindicating exercise or hypoxic exposure.
Musculoskeletal injury or illness affecting normal training or performance within the previous three months.
Current use of medications or supplements that may substantially influence physiological adaptation or exercise performance.
Failure to complete the intervention or outcome assessments according to the study protocol.
Withdrawal of informed consent at any time during the study.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Другой
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
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Экспериментальный: Alternating Altitude Training
Participants perform the prescribed training program using an alternating altitude strategy, with selected training sessions conducted under simulated higher-altitude conditions and the remaining sessions completed at the regular altitude training base.
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Participants complete the prescribed training program using an alternating altitude strategy, combining regular altitude training with selected sessions performed under simulated higher-altitude conditions.
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Активный компаратор: Fixed-Altitude Training
Participants perform the same prescribed training program entirely at the regular altitude training base throughout the intervention.
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Participants complete the prescribed training program exclusively at the regular altitude training base.
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Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Body Weight
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Body weight measured before and after the training period.
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Baseline and immediately after completion of the 4-week intervention.
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Body Fat Percentage
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Body fat percentage measured using bioelectrical impedance or other validated method.
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Baseline and immediately after completion of the 4-week intervention.
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Forced Vital Capacity (FVC)
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Forced vital capacity measured using spirometry before and after the intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Maximal Voluntary Ventilation
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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MVV measured using standard pulmonary function testing protocol pre- and post-intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Left Ventricular Volume
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Echocardiography measurement of left ventricular end-diastolic and end-systolic volume.
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Baseline and immediately after completion of the 4-week intervention.
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Ejection Fraction
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Echocardiography assessment of left ventricular ejection fraction pre- and post-training.
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Baseline and immediately after completion of the 4-week intervention.
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Myocardial Thickness
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Measurement of interventricular septum and left ventricular posterior wall thickness by echocardiography.
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Baseline and immediately after completion of the 4-week intervention.
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Maximal Oxygen Uptake
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Pre- and post-intervention measurement of VO₂max using standard exercise testing protocol to assess aerobic capacity
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Baseline and immediately after completion of the 4-week intervention.
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Countermovement Jump Height
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Countermovement jump (CMJ) height measured using a validated force platform or jump assessment system to evaluate lower-limb explosive power before and after the intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Squat Jump Height
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Squat jump (SJ) height measured using a validated force platform or jump assessment system to assess concentric lower-limb explosive strength before and after the intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Isometric Mid-Thigh Pull Peak Force
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Peak force during the isometric mid-thigh pull (IMTP) measured using a force platform to assess maximal isometric lower-limb strength before and after the intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Isometric Mid-Thigh Pull Rate of Force Development
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Rate of force development (RFD) during the isometric mid-thigh pull (IMTP) measured using a force platform before and after the intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Reactive Strength Index (RSI)
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Reactive Strength Index (RSI) calculated from repeated ankle hops using a force platform or validated jump assessment system to assess lower-limb reactive strength before and after the intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Red Blood Cell Count
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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RBC count measured from venous blood samples pre- and post-intervention.
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Baseline and immediately after completion of the 4-week intervention.
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Hemoglobin
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Hemoglobin concentration measured from venous blood samples.
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Baseline and immediately after completion of the 4-week intervention.
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Hematocrit
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Hemoglobin concentration measured from venous blood samples.
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Baseline and immediately after completion of the 4-week intervention.
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Erythropoietin
Временное ограничение: Baseline and immediately after completion of the 4-week intervention.
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Plasma EPO concentration measured from venous blood samples.
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Baseline and immediately after completion of the 4-week intervention.
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Соавторы и исследователи
Спонсор
Даты записи исследования
Изучение основных дат
Начало исследования (Оцененный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Другие идентификационные номера исследования
- AAT-RW-2026-01
Планирование данных отдельных участников (IPD)
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Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .
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