Internal Medicine Clinical Trial
Official title:
Nutrition Screening - Route to a More Practical Method
NCT number | NCT05546034 |
Other study ID # | PKL-127 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | September 6, 2021 |
Est. completion date | March 23, 2022 |
Verified date | September 2022 |
Source | University of Tartu |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Observational study. Comparison of existing nutritional screening tools based on questionnaires with blood tests already performed on a routine basis. No intervention undertaken.
Status | Completed |
Enrollment | 300 |
Est. completion date | March 23, 2022 |
Est. primary completion date | March 23, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: In-patient in department of internal medicine Exclusion Criteria: Unable to complete questionnaire or in protective isolation |
Country | Name | City | State |
---|---|---|---|
Estonia | Tartu Ülikooli Kliinikum | Tartu | Tartumaa |
Lead Sponsor | Collaborator |
---|---|
University of Tartu |
Estonia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluation of new nutrition risk screening tool (devised from 200 patients) by validation in 100 contemporaneous patients in comparison with established screening tools (MUST, NRS-2002 and SGA) and malnutrition defined by GLIM. | Established tools for screening and assessing nutritional status are utilised. These are the Malnutrition Universal Screening Tool (MUST), the Nutrition Risk Screening-2002 (NRS-2002), the Subjective Global Assessment (SGA) and the Global Leadership Initiative on Malnutrition (GLIM). Data from laboratory testing that has already been performed on these patients is extracted from their hospital records. It is hypothesised that multivariate analysis of indicative parameters will identify 6 to 12 tests that can be combined (with appropriate weighting) into a new predictive score.
300 sets of patient data will be divided on a randomised basis into a group of 200 from whom the prospective new scoring system will be devised, and a group of 100 in whom the score will be tested for validity against NRS-2002. |
Within 6 months of completion of recruitment | |
Secondary | Validation of new score against GLIM | The intended new score will be tested against GLIM. The primary validation is against NRS-2002 as the score is intended as a screening tool for high risk of malnutrition, but it is important to determine whether it is also a test of established malnutrition. | Within 6 months of completion of recruitment |
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