The study is a randomized controlled study, ongoing over 16 weeks. At discharge, the intervention group receives guidance from a clinical dietician, where an individual nutrition plan is made. The dietitian will perform a telephone follow-up after 4 and 30 days. It will also be possible for the participant, relatives or municipality to contact the dietician if nutritional questions arise. At the time of discharge the intervention group will receive a package containing foods and drinks that will cover their nutritional needs the first day after discharge. They will also get a goodiebag containing samples on protein-rich milk-based drinks. Data is collected on quality of life, appetite, physical function, dietary intake, weight, height, energy and protein needs, as well as experience of discharge and cooperation with the municipality. If there is a need, information about nutrition status will be sent to the municipality so the municipality can take over nutritional treatment. The control group receives standard treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
207
Guidance from a clinical dietician. Individual nutrition plan A package containing foods and drinks, which will cover their nutritional needs the first day after discharge. A goodiebag containing samples on protein-rich milk-based drinks. Telephone follow-up after 4 and 30 days and the possibility to call the dietician in case of questions about nutrition.
Unit for Dietetics and Nutrition Research, Herlev hosipital
Herlev, Denmark
Hospital readmissions
Time frame: 6 months
Mortality
Time frame: 30 days, 16 weeks, 6 months
Weight
Time frame: 16 weeks
Protein intake
24 hour recall
Time frame: 16 weeks
Energi Intake
24 hour recall
Time frame: 16 weeks
Appetite
SNAQ
Time frame: 16 weeks
Health related Quality of life
EQ-5D
Time frame: 16 weeks
Physical function
30-s CST
Time frame: 16 weeks
Hospital readmissions
Time frame: 30 days, 16 weeks
Combined adverse advents
Time frame: 30 days, 16 weeks, 6 months
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