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Идёт набор NCT06576895

Nutrition Practice in Critically Ill Adults

— Наблюдательное Critical Illness

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: No intervention.
Кому может быть актуально
Состояния в реестре: Critical Illness. Базовые параметры: от 18 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
Австралия
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

Nutrition Practice in Critically Ill Adults - an Observational Study

Обзор

To determine the role of nutrition in recovery from critical illness, current practice must first be understood. However, no benchmarking process currently exists for nutrition practice during critical illness, from ICU admission to hospital discharge. This vital gap requires addressing. The aim of this study is to inform and re-design models of nutrition care and generate research priorities for the future by obtaining data on nutrition provision and practice and that of consumer preference for nutrition care.

Подробное описание

This study is a multi-centre observational study of nutrition practices in critically ill adults across ANZ. Two study periods are proposed, the first confirmed period in Q3-2024 and the second in 2026.

This study is part of a larger study which consists of three interconnected streams. This study forms part of Stream 2 which is about understanding nutrition practice and provision in adults with critical illness. The findings from this study will be used to inform the development and implementation of new models of nutrition care for adults with critical illness.

On the day of study commencement (day 1), all patients treated in the ICU and admitted to the ICU after 00:00 will be screened for eligibility. Observational data will be collected days 1 and 3 of their ICU stay (whilst present in ICU) and then days 7, 14, 21 and 28 (whether they are in ICU or the ward) as well as the first full day on the ward (day after ICU discharge).

At the completion of the project, the investigators will hold the largest sample of nutrition care in critical illness in Australia (approximately 1200 Adult patients including the pilot data period) and the only international database to include the period after ICU discharge. This proposal directly links with the National Safety and Quality Health Service (NSQHS) Standard 5 (Comprehensive Care) and Standard 2 (Partnering with Consumers) and will rapidly provide data about nutrition care and hospital acquired malnutrition (a serious reportable consequence under Standard 5) to inform the accreditation process and provide a risk mitigation strategy to prevent malnutrition before it occurs. This data will be used to improve and re-design nutrition care, as well as generate new research priorities that are highly relevant to issues within clinical care, with the potential to save millions of dollars in healthcare expenditure nationally.

Вмешательства

  • Другое No intervention
    No intervention

Первичные конечные точки

  • Nutritional outcomes [Срок оценки: Up to day 28 of hospitalization]
  • Nutritional outcomes [Срок оценки: Up to day 28 of hospitalization]
  • Nutritional outcomes [Срок оценки: Up to day 28 of hospitalization]
  • Nutritional outcomes [Срок оценки: Up to day 28 of hospitalization]
  • Nutrition service delivery in the ICU and ward setting [Срок оценки: Up to day 28 of hospitalization]
  • Descriptions of nutrition prescription, delivery and service variability across ANZ [Срок оценки: Up to day 28 of hospitalization]
  • Patient-centred outcomes [Срок оценки: Up to day 28 of hospitalization]
  • Patient-centred outcomes [Срок оценки: Up to day 28 of hospitalization]
  • Patient-centred outcomes [Срок оценки: Up to day 28 of hospitalization]

Критерии участия

Критерии включения

  • Age 18 years or older
  • Admitted to ICU after 00:00 on the date of study commencement
  • Remain in ICU for ≥ 48 hours

Критерии исключения

  • Patients who have been deemed ready to be discharged by the treating team within 48 hours of ICU admission but have not been able to be discharged within 48 hours of ICU admission for logistical reasons (e.g., due to bed unavailability, inability to return home)
  • Patients who have been admitted for palliative care or organ donation or made palliative within 48 hours of ICU admission

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Случай-контроль

Центры проведения

Австралия · 1 центр
  • Monash University — Melbourne

Идентификаторы

NCT: NCT06576895 · ANZIC-RC/ER002

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗