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Clinical Trials/NCT03412695
NCT03412695
Completed
Not Applicable

Development of a Decision Support System to Prevent and Treat Disease-related Malnutrition

Oslo University Hospital1 site in 1 country100 target enrollmentAugust 22, 2018
ConditionsMalnutrition

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malnutrition
Sponsor
Oslo University Hospital
Enrollment
100
Locations
1
Primary Endpoint
Change in body weight (kg) during hospital stay
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The prevalence of disease-related malnutrition among hospitalized patients is 30-50%. There is a lack of tools to follow up the nutritional treatment of these patients. The investigators develop the decision support system "MyFood" which can be used to assess patients' dietary intake, evaluate intake against individual needs, and propose nutrition related measures and an individual nutrition plan for each patient. The investigators will study the clinical effects of using MyFood among hospitalized patients. In addition the implementation of the tool among healthcare workers will be studied.

Detailed Description

The prevalence of disease-related malnutrition among hospitalized patients is 30-50%. Disease-related malnutrition increase the morbidity and mortality among patients and leads to longer length of stay. There is a lack of tools to follow up the nutritional treatment of patients at nutritional risk. The decision support system "MyFood" is developed in the project with the purpose to prevent and treat disease-related malnutrition. MyFood includes 4 modules: 1) A function to register patient needs and symptoms, 2) Dietary assessment function, 3) Automatic evaluation of dietary intake compared to individual needs, 4) Feedback, including a report on intake of energy, protein, and liquids compared to individual needs, and recommendations for nutritional measures and an individual nutrition plan. Clinical effects of using MyFood among hospitalized patients will be studied in a randomized controlled trial. In addition, the implementation of the tool among nurses and other healthcare workers will be explored.

Registry
clinicaltrials.gov
Start Date
August 22, 2018
End Date
May 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Oslo University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Mari Mohn Paulsen

Project coordinator

Oslo University Hospital

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • \<72 hours expected hospital stay
  • Terminal patients
  • Psychiatric patients
  • Patients who cannot read the Norwegian Language
  • Patients diagnosed with: sickle cell anemia, haemophilia, or deep vein thrombosis

Outcomes

Primary Outcomes

Change in body weight (kg) during hospital stay

Time Frame: 2 times each week, from patient admission (day 1) to hospital discharge (on average day 11)

Measured standing on an electronic scale

Secondary Outcomes

  • Proportion of patients who get implemented nutrition-related measures(Assessed from medical journals every second day during each patient's hospital stay (11 days on average))
  • Proportion of patients who receive a nutrition plan(Assessed from the participating patients' medical journals on day 2 and every second day during hospital stay (11 days on average))
  • Re-admissions(30 days after discharge)
  • Patient length of hospital stay(At the day of patient discharge (on day 11))
  • Change in body Composition(2 times each week, from patient admission (day 1) to hospital discharge (on average day 11))
  • Proportion of patients who receives a nutrition diagnose(Assessed from medical journals every second day during each patient's hospital stay (11 days on average))
  • Patient generated subjective global assessment (PG-SGA) score(Measured on day 1 and at admission (day 11 on average))

Study Sites (1)

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