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Fortified Hospital Food as Nutritional Support (DHH)

2012年12月12日 更新者:Copenhagen University Hospital at Herlev

Positive Effect of Fortified Hospital Food on Nutritional Intake in Patients at Nutritional Risk. A Randomized Controlled Trial.

Background:

The investigators have previously documented that patients at nutritional risk lack sufficient energy and protein intake. In 2009 the investigators conducted a non-randomized historically controlled intervention study of 40 patients at nutritional risk. The study indicated that a tailored food concept increased nutritional intake in this patient group.

The objective of the current study is therefore to investigate these findings in a randomized clinical trial. Our target is for 75% of patients in the intervention group to reach 75% of their energy and protein requirements.

Methods:

The study will compare standard nutritional care (control group) with tailored nutritional care (the possibility to order small energy and protein-enriched dishes called "Delights of Herlev Hospital"). 96 patients at nutritional risk, according to the NRS-2002 criteria, will be included in the study.

研究概览

研究类型

介入性

注册 (实际的)

84

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Copenhagen
      • Herlev、Copenhagen、丹麦、2730
        • Herlev University Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • patients at nutritional risk, according to the NRS-2002 system
  • patients must be able to understand the information and be able to give a written informed consent (sufficient cognitive functioning)
  • well-functioning gastrointestinal tract
  • anticipated length of hospitalization of more than 3 days

Exclusion Criteria:

  • terminal patients
  • dysphagia
  • food allergy or intolerance

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Nutritional intervention
The study will compare standard nutritional care (control group) with tailored nutritional care (the possibility to order small energy and protein-enriched dishes called "Delights of Herlev Hospital")(intervention group).
The study is af 12 week randomized clinical trail with inclusion of 96 patients at nutritional risk, according to the NRS-2002 system. The intervention group is is given a tailored nutritional care(the possibility to order small energy and protein-enriched dishes called "Delights of Herlev Hospital").

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
The primary endpoint was the percentage of patients reaching >75% of their protein and energy requirements.
大体时间:Energy and protein intake will be calculated on an average of 3 and up to 7 days of dietary. Number of days of food intake recording depends on how long the patient is hospitalized.

The patients energy requirement will be estimated both from the factorial method and by Harris and Benedicts formula. Protein requirement will be 18E% of the energy requirement.

Recording of the dietary intake will be carried out on a daily basis over a periode of minimum 3 days and maxium 7 days

Energy and protein intake will be calculated on an average of 3 and up to 7 days of dietary. Number of days of food intake recording depends on how long the patient is hospitalized.

次要结果测量

结果测量
措施说明
大体时间
handgrip strength
大体时间:at day 3, 5 and 7
Handgrip strength (HGS)will be measured with a Jamar Digital Hand Dynanometer. HGS will only be measured in the right hand because the right hand i significantly stronger in right-handed subjects and there is no significant difference between the two sides in left-handed subjects. Subjects will be encouraged to perform maximal contractions three times with a 15-s interval and the average value will be recorded.
at day 3, 5 and 7
average daily energy and protein intake
大体时间:Patient und energy and protein intake will be followed during hospitalization from enrollment in the study and until discharge or up to 7 days
Patient und energy and protein intake will be followed during hospitalization from enrollment in the study and until discharge or up to 7 days
Use of tube feeding
大体时间:The patients use of tube feeding will be followed from enrollment in the study and until discharge, an expected average of 9 days.
Use of tube feeding will be registrated (yes or no and amount (ml.)
The patients use of tube feeding will be followed from enrollment in the study and until discharge, an expected average of 9 days.
use of parenteral nutrition
大体时间:The patients use of parenteral nutrition will be followed from enrollment in the study and until discharge, an expected average of 9 days.
Registration of use of parenteral nutrition (yes or no). If yes how much (ml.).
The patients use of parenteral nutrition will be followed from enrollment in the study and until discharge, an expected average of 9 days.
length of stay
大体时间:an expected average of 9 days.
an expected average of 9 days.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Tina Munk, MSc.、Herlev University Hospital, Denmark

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2011年10月1日

初级完成 (实际的)

2012年2月1日

研究完成 (实际的)

2012年2月1日

研究注册日期

首次提交

2011年7月19日

首先提交符合 QC 标准的

2011年8月11日

首次发布 (估计)

2011年8月12日

研究记录更新

最后更新发布 (估计)

2012年12月13日

上次提交的符合 QC 标准的更新

2012年12月12日

最后验证

2012年12月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • H-1-2011-048

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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