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Идёт набор NCT05413616

The Effect of a Combined Personalized Nutritional Intervention and a Personalized Graded Activity Functional Training Program on Physical Performance in Hospitalized Older Patients, Compared to Usual Care

Без фазы С лечением Old Age; Atrophy

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: FITFOOD lifestyle intervention.
Кому может быть актуально
Состояния в реестре: Old Age; Atrophy. 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 →
Официальное название

The Effect of a Combined Personalized Nutritional Intervention and a Personalized Graded Activity Functional Training Program on Physical Performance in Hospitalized Older Patients, Compared to Usual Care: A Randomized Clinical Trial

Обзор

This project aims to improve physical performance in older patients, by offering a personalized combined nutritional intervention with a physical activity training program. The intervention starts at hospital admittance and is continued after discharge in the home care setting, supported by an e-health application.

Подробное описание

Rationale: The older hospitalized population is growing and specifically at risk for decreased muscle mass and physical functioning and has a negative influence on activities of daily living, independence, quality of life, re-admissions, and nursing home placement. Current knowledge shows that a physical activity training programs consisting of tailored resistance and endurance exercise can improve muscle mass in healthy elderly. Nutritional interventions in conjunction with physical activity based on individual protein requirements, high quality protein and timing of protein intake can further stimulate muscle protein synthesis. The effect of a combined nutritional intervention with physical activity in healthy individuals and athletes has been studied before, but not in older hospitalized patients. A personalized combined physical activity program and a nutritional intervention could be a solution and is an exciting emerging field of research with the potential to dramatically improve patient outcomes.

The average hospital admittance is 4 to 5 days in which the prevention of the decline in muscle mass and physical performance can be initiated but not improved. Thus, the translation of a prolonged combined intervention to home care is essential. To support the combined personalized nutritional intervention and physical exercise intervention during hospitalization and home care, an eHealth application for and with older patients can be beneficial.

Objective: This project aims to improve physical performance in older patients, by offering a personalized combined nutritional intervention with a physical activity training program. The intervention starts at hospital admittance, and is continued after discharge in the home care setting, supported by an e-health application.

Study design: The study will be performed as a randomized clinical trial. Study population: The study population hospitalized adult patients of ≥65 years, living in the Nijmegen area within the Radboud University Medical Centre.

Intervention: One group receives a personalized nutritional intervention by a dietician combines with a functional training program by physical therapists. The nutritional intervention focuses on adequate protein intake, type, and timing of protein. The exercise program will make use of goal setting throughout the intervention period to optimize the training effect . The control group will receive usual care.

Study parameters: The primary study outcome is based on the difference in change in physical performance between baseline and after 3 months of intervention of the intervention and the control group (usual care). This will be analyzed using multilevel mixed model corrected by potential confounders, measured by the Timed up \& Go test (TUG), a sensitive tool to measure physical performance in elderly.

Secondary: As a secondary outcome, the effect on short physical performance battery, muscle strength, muscle mass, nutritional status, movement, independence, quality of life, clinical outcomes and cost-effectiveness will be studied.

Nature and extent of the burden and risks associated with participation, benefit, and group relatedness: Study measurements are non-invasive. This study will not confer any no additional risks. The intervention will start at hospital admittance and will be continued after discharge in the home setting by a dietician and physiotherapist in their nearby home, which keeps the burden for the patient relatively low and is an extra service for the patient. Protein supplementation will be delivered within the save amounts. Possible serious reactions to the intervention will be noted as SAE's.

Вмешательства

  • Поведенческое FITFOOD lifestyle intervention
    Lifestyle intervention with a nutritional and exercise component.

Первичные конечные точки

  • Change in Timed Up & Go [Срок оценки: Baseline, 1 day before hospital release, 4 weeks after baseline, 12 weeks after baseline, 24 weeks after baseline.]
Вторичные конечные точки (12)
  • Change in Short Physical Performance Battery [Срок оценки: Baseline, 1 day before hospital release, 4 weeks after baseline, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in muscle strength [Срок оценки: Baseline, 1 day before hospital release, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in muscle mass [Срок оценки: Baseline, 1 day before hospital release, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in nutritional status [Срок оценки: Baseline, 1 day before hospital release, 4 weeks after baseline, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in nutritional intake (energy, protein). [Срок оценки: Baseline, 1 day before hospital release, 4 weeks after baseline, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in movement according to actometer [Срок оценки: Baseline, 1 day before hospital release, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in activities of daily living [Срок оценки: Baseline, 1 day before hospital release, 12 weeks after baseline, 24 weeks after baseline.]
  • Change in quality of life [Срок оценки: Baseline, 1 day before hospital release, 12 weeks after baseline, 24 weeks after baseline.]
  • Clinical outcomes: length of hospital stay [Срок оценки: 24 weeks after baseline]
  • Clinical outcomes: re-admission [Срок оценки: 24 weeks after baseline]
  • Clinical outcomes: complications [Срок оценки: 24 weeks after baseline]
  • Clinical outcomes: mortality [Срок оценки: 24 weeks after baseline]

Критерии участия

Критерии включения

  • Aged ≥65 years
  • Living within the Nijmegen area (within 40km)
  • Admitted to clinical ward of Radboudumc or CWZ
  • Understanding and speaking of the Dutch language
  • Mentally competent
  • Signed informed consent

Критерии исключения

  • Complete use of tube feeding or parenteral nutrition
  • Renal insufficiency (MDRD-GFR < 30ml/min)

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
Открытое
Основная цель
Лечение

Центры проведения

Нидерланды · 1 центр
  • Sabien van Exter — Nijmegen

Публикации

  • van Exter SH, Koenders N, van der Wees PJ, Drenth JPH, van den Berg MGA. Lessons learned from a combined, personalized lifestyle intervention in hospitalized patients at risk for sarcopenia: a feasibility study. Disabil Rehabil. 2025 Jul;47(14):3679-3686. doi: 10.1080/09638288.2024.2426685. Epub 2024 Nov 12. PMID 39530465

Идентификаторы

NCT: NCT05413616 · 2020-6664

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗