Under Nutrition Clinical Trial
Official title:
The Effect of Follow up on Nutrition Intervention After Discharge in Undernourished Geriatric Patients
The purpose of this study is to test two different interventions of nutrition follow up
after discharge from geriatric ward in undernourished geriatric patients. The patients are
randomized to a home visit arm, a telephone consultation arm, or a control arm. Patients in
the home visit arm and their home care helper will get visits from a clinical dietician at
one week, two weeks and four weeks after discharge, in order to follow up on the nutrition
intervention. Patients in the telephone consultation arm and their home care helper will be
contacted by a clinical dietician at one week, two weeks and four weeks after discharge, in
order to follow up on the nutrition intervention. The control arm will not be contacted.
The primarily outcome is functional ability. Secondary outcomes are quality of life,
readmission and mortality.
Under nutrition among geriatric patients is a recurrent and well documented problem. Up to 55 % of the elderly are undernourished at the time of admission. Hospitalisation and acute illness are associated to loss of muscles and physical ability, complications, dependency, morbidity and mortality. Elderly who live alone are more vulnerable to nutritional problems, than elderly who live together with another person or in a nursing home. Geriatric patients, who are admitted to geriatric ward Aarhus University Hospital due to various acute somatic disorders, aged 75 and older and who are living alone with help from the home care facilities can participate in the study. According to the power calculation 150 patients must be included, 50 patients in each arm of the study. Informed consent will be obtained before inclusion and discharge from hospital. Randomization will be computerised and determine if the patient will be allocated to the "home visit" group, the "telephone consultation" group or the "control group". Patients who suffer from mental disorder (MMSE<22) or active cancer are excluded as well as patients who live together with another person or live in a nursing home. During hospitalisation the three groups will receive the same nutritional care as all patients in nutritional risk. This includes nutritional intervention during hospitalization and an individual diet plan at discharge. Patients in the home visit arm will get visits from a clinical dietician at one week, two weeks and four weeks after discharge. Patients in the telephone consultation arm will be contacted by a clinical dietician at one week, two weeks and four weeks after discharge. In both intervention groups the patients and their home care helpers will get dietary advice and follow up on their individual diet plan. The main outcome is functional ability from discharge and to 8 weeks after discharge. Secondary outcomes are quality of life, readmission at 30 and 90 days and mortality at 30 and 90 days. ;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Active, not recruiting |
NCT02457923 -
Mobile -Solutions Aiding Knowledge for Health Improvement
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N/A |