Acute Exercise Responses With Blood Flow Restriction Under Dynamic Pressure Compared to Fixed Pressure in Patients With Severe Gonarthrosis
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-intensity resistance exercise with moderate arterial occlusion pressure and dynamic pressure., Low-intensity resistance exercise with moderate arterial occlusion pressure and fixed pressure., Moderate-intensity resistance exercise with low arterial occlusion pressure and dynamic pressure., Moderate-intensity resistance exercise with low arterial occlusion pressure and fixed pressure..
- Кому может быть актуально
- Состояния в реестре: Severe Knee Osteoarthritis. Базовые параметры: 50 лет — 85 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
Acute Responses to Different Blood Flow Restriction Exercise Configurations With Dynamic Pressure Compared to Fixed Pressure in Patients With Severe Gonarthrosis
Обзор
This study aims to evaluate the acute effects of blood flow restriction (BFR) training on hypoalgesia and neuromuscular responses in patients with severe gonarthrosis by comparing the application of pressure with a dynamic versus a fixed configuration. There will be six different training conditions with varying levels of blood flow occlusion (%BFR) and percentage of load (%RM): 1) 30% RM and 50% BFR with dynamic pressure; 2) 30% RM and 50% BFR with fixed pressure; 3) 50% RM and 50% BFR with dynamic pressure; 4) 50% RM and 50% BFR with fixed pressure; 5) 30% RM and 80% BFR with dynamic pressure; 6) 30% RM and 80% BFR with fixed pressure. Each participant will complete six individual sessions under different training conditions, assigned in a random order with a 72-hour interval between each session.
Вмешательства
- Устройство Low-intensity resistance exercise with moderate arterial occlusion pressure and dynamic pressure.
A single quadriceps extension exercise at 30% of 1 repetition maximum (1RM) with dynamic occlusion at 50% of limb occlusion pressure (LOP), performing 4 sets of 30, 15, 15, 15 repetitions with 30 seconds of rest between sets. - Устройство Low-intensity resistance exercise with moderate arterial occlusion pressure and fixed pressure.
A single quadriceps extension exercise at 30% of 1RM with fixed occlusion at 50% of limb occlusion pressure (LOP), performing 4 sets of 30, 15, 15, 15 repetitions with 30 seconds of rest between sets. - Устройство Moderate-intensity resistance exercise with low arterial occlusion pressure and dynamic pressure.
A single quadriceps extension exercise at 50% of 1RM with dynamic occlusion at 30% of limb occlusion pressure (LOP), performing 4 sets of 30, 15, 15, 15 repetitions with 30 seconds of rest between sets. - Устройство Moderate-intensity resistance exercise with low arterial occlusion pressure and fixed pressure.
A single quadriceps extension exercise at 50% of 1RM with a fixed occlusion of 30% of the limb occlusion pressure (LOP), performing 4 sets of 30, 15, 15, 15 repetitions with 30 seconds of rest between sets. - Устройство Low-intensity resistance exercise with high arterial occlusion pressure and dynamic pressure.
A single quadriceps extension exercise at 15% of 1RM with a dynamic occlusion of 80% of the limb occlusion pressure (LOP), performing 4 sets of 30, 15, 15, 15 repetitions with 30 seconds of rest between sets. - Устройство Low-intensity resistance exercise with high arterial occlusion pressure and fixed pressure.
A single quadriceps extension exercise at 15% of 1RM with a fixed occlusion of 80% of the limb occlusion pressure (LOP), performing 4 sets of 30, 15, 15, 15 repetitions with 30 seconds of rest between sets.
Первичные конечные точки
- Pain intensity at rest (Visual Analogue Scale, 0-10) [Срок оценки: Periprocedural]
Вторичные конечные точки (7)
- Pressure pain threshold [Срок оценки: Periprocedural]
- Perceived exertion scale (The BORG CR10 Scale) [Срок оценки: Periprocedural]
- Surface electromyography [Срок оценки: Periprocedural]
- Occurrence of adverse effects [Срок оценки: Immediately after the intervention, 72 hours later, and two weeks after the study ended.]
- Kinesiophobia (The Tampa Scale for Kinesiophobia) [Срок оценки: Baseline]
- Pain catastrophizing [Срок оценки: Baseline]
- Functional Measure (Western Ontario and McMaster Universities Osteoarthritis Index) [Срок оценки: Baseline]
Критерии участия
Критерии включения
- Age between 50 and 85 years
- Diagnosis of severe gonarthrosis according to the clinical and radiographic criteria of the American College of Rheumatology guidelines.
- On the waiting list for unilateral total knee replacement (TKR) surgery
Критерии исключения
- Pain in the contralateral leg with an intensity ≥80/100 mm on the visual analog scale (VAS) during daily activities.
- Previous hip or knee replacement surgery and osteotomy within the last year.
- Autoimmune arthritis
- Medical conditions that contraindicate exercise.
- Participation in exercise programs (>2 days/week with training at intensities of 10-15 1RM) in the previous six months.
- History of stroke, brain surgery, major depression, or self-reported cognitive impairment that could affect performance in the study.
- Cardiovascular, thrombotic, or vascular risk factors (uncontrolled hypertension, peripheral arterial disease, history of deep vein thrombosis or pulmonary embolism, heart failure, severe varicose veins, or uncontrolled anticoagulant therapy).
- Skin or local alterations at the cuff application site (ulcers, open wounds, infections, lymphedema, or severe edema).
- Inability to communicate normally or with impaired communication skills.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Перекрёстный дизайн
- Маскирование
- Двойное слепое
- Основная цель
- Лечение
Центры проведения
Испания · 1 центр
- University of Valencia — Valencia
Идентификаторы
NCT: NCT07316933 · 2025-FIS-3955989