Rehabilitation After a Hip Fracture: the Effects of Dietary Protein and Exercise on Bone and Muscle Health and Quality of Life
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: Protein-enriched diet, Progressive resistance exercise.
- Кому может быть актуально
- Состояния в реестре: Hip Fractures. Базовые параметры: от 65 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
- Нидерланды
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
Hip fractures often lead to functional limitations, loss of independence, weight loss and decreased well-being. Only half of the patients regain their functional level and 24% die within the following year. Financial consequences are significant due to costly surgery and long-term care. Hip fracture incidence is expected to increase sharply due to the ageing population, reducing accessibility to and quality of rehabilitation care. Therefore, optimizing treatment is essential. Previous protein and exercise studies showed improved muscle and bone health in healthy or frail community-dwelling older adults, but effects in older hip fracture patients are not known. Better rehabilitation may improve bone and muscle health, nutritional status, quality of life, lower costs and lower burden for healthcare. The overall objective is to investigate the effectiveness, costs and cost-effectiveness of a protein-enriched diet and resistance exercise for 3 months compared to usual care on bone and muscle health, and quality of life in older adults recovering from an acute hip fracture.
Вмешательства
- Другое Protein-enriched diet
A protein intake of 1.5 g/kg bodyweight/day. This will be obtained by consuming protein-rich and protein-enriched foods. - Другое Progressive resistance exercise
The intervention group will perform resistance training during three non-consecutive days with a minimum of 48 hours between the sessions. Subjects will continue the resistance training after discharge for 2 times a week, also with a minimum of 48 hours between sessions until the study period of 3 months is completed. All sessions will be supervised by physiotherapists.
Первичные конечные точки
- Physical Functioning [Срок оценки: Physical performance measurements will be performed at baseline, after discharge from the rehabilitation centre (varies per participant, on average after 1 month), and after 3 months.]
Вторичные конечные точки (10)
- Handgrip strength [Срок оценки: Handgrip strength will be measured at baseline, after discharge from the rehabilitation centre (varies per participant, on average after 1 month), and after 3 months.]
- Muscle mass [Срок оценки: The DEXA scans will be performed at baseline and after 3 months.]
- Bone Mineral Density [Срок оценки: The DEXA scans will be performed at baseline and after 3 months.]
- Bone Mineral Density [Срок оценки: The quantitative ultrasound measurements will be performed at baseline and after 3 months.]
- Quality of life [Срок оценки: Quality of life will be assessed at baseline, after discharge from the rehabilitation centre (varies per participant, on average after 1 month), and after 3 months.]
- Blood markers [Срок оценки: Blood markers will be measured at baseline, after discharge from the rehabilitation centre (varies per participant, on average after 1 month), and after 3 months.]
- Inpatient rehabilitation time [Срок оценки: Assessed at discharge from the rehabilitation centre (varies per participant, on average after 1 month).]
- Daily life functioning [Срок оценки: Daily life functioning will be assessed at baseline, after discharge from the rehabilitation centre (varies per participant, on average after 1 month), and after 3 months.]
- Nutritional Status [Срок оценки: This measurement will be performed at baseline, after discharge from the rehabilitation centre (varies per participant, on average after 1 month), and after 3 months.]
- Costs [Срок оценки: This will be assessed after 3 months.]
Критерии участия
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Age ≥ 65 years
- Acute hip fracture
- Able to give written informed consent
- Mentally competent, as judged by the treating physician
- Admission to a rehabilitation centre that participates in this research
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Allergic, intolerant or hypersensitive to milk/lactose (self-reported)
- Not willing to stop using dietary supplements with exception of calcium and vitamin D
- Pathological fracture or periprosthetic fracture
- Abnormal hepatic or renal laboratory parameters, such as estimated glomerular filtration rate (eGFR) <30 ml/min/1,73 m2 (data from hospital)
- Diagnosis of disorders/diseases where a high protein intake can be harmful, such as renal impairment or failure, or liver disease (geriatric care physician has the decisive voice)
- Diagnosis of bone metabolic disorders such as primary hyperparathyroidism, Paget's disease, or myeloma.
- Taking medication other than bisphosphonates known to strongly alter bone, calcium or muscle metabolism, such as oestrogen, hormone replacement therapy, corticosteroids, anabolic agents, or calcitonin.
- Disorders/diseases which may affect ability to follow study protocol and which cannot be overcome with help of a caregiver
- Current participation in other scientific research
- No permission to request information from the general practitioner/ treating specialist(s) about medical history, medication use, liver and kidney values, and details about the broken hip
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Простое слепое
- Основная цель
- Лечение
Центры проведения
Нидерланды · 2 центра
- Rijnstate Hospital — Arnhem
- Gelderse Vallei Hospital — Ede
Идентификаторы
NCT: NCT07036341 · NL68932.081.19