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Clinical Trials/NCT01415635
NCT01415635
Completed
Not Applicable

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

Copenhagen University Hospital at Herlev1 site in 1 country84 target enrollmentOctober 2011
ConditionsMalnutrition

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malnutrition
Sponsor
Copenhagen University Hospital at Herlev
Enrollment
84
Locations
1
Primary Endpoint
The primary endpoint was the percentage of patients reaching >75% of their protein and energy requirements.
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
February 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Copenhagen University Hospital at Herlev
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

The primary endpoint was the percentage of patients reaching >75% of their protein and energy requirements.

Time Frame: 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

Secondary Outcomes

  • handgrip strength(at day 3, 5 and 7)
  • average daily energy and protein intake(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(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(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(an expected average of 9 days.)

Study Sites (1)

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