Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 10:56 PM
Ignite Modification Date:
2025-12-24 @ 10:56 PM
NCT ID:
NCT07234669
Brief Summary:
The study investigates whether clinical dietitians at a hospital ward can improve patients' dietary intake during hospitalisation, and whether it can prevent patients from being admitted efter discharge and improve their prognosis. Dietary intake will be measured daily and readmittance within 30 days from discharge will be registered. Questionnaires will be used to assess patients' satisfaction with nutritional care during hospitalisation.
Detailed Description:
Clinical dietitians have been an integrated part of the medical pulmonary ward at Gødstrup Hospital since early 2022. They carry out nutritional screening, nutritional treatment and assisst and guide patients in ordering of meals from the hospital's flexible á la carte food service concept.
The study aims to evaluate the effect of the clinical dietitians' effort on patients nutritional intake, risk of readmittance after discharge and 30-days mortality.
The study is observational, and no changes to the current standard of nutritional care will be implemented throughout the study period. Nutritional intake will be measured daily throughout hospitalisation. Readmittances and vital status will be measured at day 30.
To evaluate the effect of the dietitians' effort, data will be compared to historical data from a previous completed study at the same ward.
Patient satisfaction with nutrional care during hospitalisation will be measured with a purpose-designed questionnaire.
Informed written consent will be obtained from all patients before inclusion, and they will be informed that their partitipation is voluntary and that they can withdraw their consent at anytime.
Study:
NCT07234669
Study Brief:
Protocol Section:
NCT07234669