- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07683091
Machine Learning-Guided Training for Elite Athletes (MLGT) (MLGT)
A Machine Learning-Guided Training Approach to Reduce Injuries and Enhance Performance in Elite Athletes: A Prospective Cohort Evaluation
Plaintext The purpose of this study is to evaluate whether a personalized training protocol driven by machine learning can successfully reduce time-loss sports injuries and enhance athletic performance in elite athletes.
During a 9-month competitive sports season, a group of elite athletes was divided into two training
Обзор исследования
Статус
Условия
Вмешательство/лечение
Подробное описание
This study evaluated the efficacy of an adaptive, machine learning-driven training protocol compared to traditional athletic preparation over a full 9-month competitive sports season. The primary objective was to determine if a dynamic, technology-led approach to training load management could minimize time-loss injuries while concurrently optimizing athletic performance markers.
Participants were elite athletes randomly allocated into two parallel groups:
- The Experimental Group, which underwent training regimens dynamically adjusted using a machine learning algorithm that analyzed individual biomechanical data and historical workload parameters to optimize training volume and intensity.
- The Control Group, which followed standard, predetermined high-performance athletic training protocols typical for competitive season preparation.
Throughout the 9-month intervention period, daily tracking was maintained by technical and coaching staff. Data collection focused on the incidence, severity, and duration of all time-loss sports injuries. Concurrently, sport-specific performance parameters were periodically assessed to evaluate physical conditioning and competitive readiness. Statistical analyses were subsequently conducted to compare cumulative injury rates, total days lost to injury, and net performance adaptations between the two cohorts.
Тип исследования
Регистрация (Действительный)
Фаза
- Непригодный
Контакты и местонахождение
Места учебы
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Shewa
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Debre Berhan, Shewa, Эфиопия, 445
- Dr. Arefayne
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Debre Berhan, Shewa, Эфиопия, 445
- M Dessye
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
Принимает здоровых добровольцев
Описание
Inclusion Criteria:
- Must be a competitive, elite-level or sub-elite track and field athlete specializing in short-to-mid distance running events.
- Aged between 18 and 35 years old.
- Actively participating in structured athletic training programs for at least 2 years prior to enrollment.
- Free from any acute musculoskeletal injuries or medical conditions that prevent full participation in high-intensity training protocols.
- Capable and willing to provide written informed consent to participate in the study.
Exclusion Criteria: 1. Current or recent (within the past 3 months) major lower-limb injury or surgery that restricts maximal sprint or aerobic performance.
2. Concurrent use of performance-enhancing drugs or medications that influence metabolic or cardiovascular responses.
3. Inability to maintain consistent participation in the designated training protocols due to scheduling conflicts or travel.
4. Any underlying cardiovascular, respiratory, or systemic condition that creates a health risk during exhaustive exercise testing.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Профилактика
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
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Активный компаратор: Control Cohort
Elite adolescent sprinters who followed standard, predetermined high-performance athletic training protocols typical for competitive season preparation.
This group received structured training volume and intensity matching standard athletic coaching guidelines, without any machine learning interventions or adaptive workload adjustments.
|
A personalized, data-driven training intervention where athletic workloads are dynamically adjusted based on predictive modeling.
The protocol continuously tracks individual physiological markers, biomechanical data, and workload history to optimize training volume and intensity.
This adaptive approach aims to maximize performance gains while minimizing the risk of overtraining and injury during the competitive season.
|
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Экспериментальный: Algorithmic Cohort
Elite adolescent sprinters who received a personalized training protocol dynamically optimized by a machine learning algorithm.
The framework evaluated individual biomechanical variables, morning heart rate variability (HRV), sleep quality, and physiological fatigue metrics to adjust training volume and intensity.
|
A personalized, data-driven training intervention where athletic workloads are dynamically adjusted based on predictive modeling.
The protocol continuously tracks individual physiological markers, biomechanical data, and workload history to optimize training volume and intensity.
This adaptive approach aims to maximize performance gains while minimizing the risk of overtraining and injury during the competitive season.
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Changes in Sprint Performance Time
Временное ограничение: 12 weeks
|
Sprint performance will be assessed using electronic timing gates to record running times over a specific distance from a stationary start.
Lower times indicate improved sprint performance.
Measurements will be taken at baseline and at the conclusion of the training intervention period to evaluate the impact of the workload protocols.
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12 weeks
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Соавторы и исследователи
Спонсор
Следователи
- Главный следователь: Dr. Arefayne M Dessye, PhD, Debre Berhan Univeristy
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Действительный)
Завершение исследования (Действительный)
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
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- DBU-SS-2023-008
- IRB#DBU-SS-2023-008 (Идентификатор реестра: ClinicalTrials.gov)
Планирование данных отдельных участников (IPD)
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Описание плана IPD
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. .