BFR Training on Muscle Morphology
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: Low load-BFRt, Sham Low load-BFRt, High load-Eccentric training.
- Кому может быть актуально
- Состояния в реестре: Blood Flow Restriction Training, Eccentric Training, Muscle Morphology, Patellofemoral Pain Syndrome. Базовые параметры: 15 лет — 35 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
- Индонезия
- 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 Blood Flow Restriction Training on Muscle Morphology and Prevention of Patellofemoral Pain Syndrome and Anterior Cruciate Ligament Injury
Обзор
This randomized clinical trial study compares high-load eccentric training (HL-Et), sham LL-BFRt, and low-load blood flow restriction (LL-BFRt) in sportsmen. The primary inquiries it seeks to address are: Is LL-BFR superior to HL-Et and sham LL-BFRt in terms of improving muscle morphology? Is LL-BFR a more effective Patellofemoral Pain Syndrome and ACL injury preventive than HL-Et and sham LL-BFRt? The three intervention groups that will be randomly assigned to participants are LL-BFRt, sham LL-BFRt, and HL-Et. Participants are expected to carry out: Participants in LL-BFRt will be required to perform LL eccentric training at 30% of their repetition maximum (RM) and 70% of their artery occlusion pressure (AOP). This training will include stairs, single leg squat, and single leg deadlift. Participants in HL-Et will be required to perform LL eccentric training at 70% of their maximum number of repetitions (RM). In order to determine whether muscular morphology and the prevention of Patellofemoral Pain Syndrome and ACL injury improve following the interventions and follow-up, researchers will compare LL-BFRt, sham LL-BFRt, and HL-Et.
Вмешательства
- Процедура Low load-BFRt
The participants' two legs will be subjected to 70% arterial occlusion pressure when the physical therapist applies the BFR cuffs. After that, participants will be required to complete eccentric exercises with a maximum repetition count of 30%, such as stairs, single leg squat, and single leg deadlift. - Процедура Sham Low load-BFRt
The participants' two legs will be subjected to 10% arterial occlusion pressure when the physical therapist applies the BFR cuffs. After that, participants will be required to complete eccentric exercises with a maximum repetition count of 30%, such as stairs, single leg squat, and single leg deadlift. - Процедура High load-Eccentric training
The physical therapist will instruct the participants to complete eccentric exercises at a maximum of 70% repetitions, such as stairs, single leg squat, and single leg deadlift.
Первичные конечные точки
- Muscle cross-sectional area [Срок оценки: 8 weeks]
- Vastus medial obliques fiber angle [Срок оценки: 8 weeks]
- Patella position [Срок оценки: 8 weeks]
Вторичные конечные точки (2)
- Incidence of patellofemoral pain syndrome [Срок оценки: 1 year]
- Incidence of anterior cruciate ligament injury [Срок оценки: 1 year]
Критерии участия
Критерии включения
- Being between the ages of 15 and 35
- Play level 1 sports (fight martial arts, basketball, futsal, and soccer) at least twice a week
- Never experienced an Patellofemoral Pain Syndrome or ACL injury before
- Never experienced a grade III sprain or strain
- Consent to participate in the study until its conclusion and provide informed consent.
Критерии исключения
- Having a tumor, cancer, vena thromboembolic disease, obesity, diabetes, hypertension, anemia, and renal failure
- Disabilities or those who are disabled.
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
- Двойное слепое
- Основная цель
- Лечение
Центры проведения
Индонезия · 1 центр
- Physical therapy laboratory, College of Medicine, Universitas Udayana and ROM Physiotherap — Denpasar
Идентификаторы
NCT: NCT06566950 · 1791/UN14.2.2.VII.14/LT.2024