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Clinical Trials/NCT03488329
NCT03488329
Completed
N/A

Effect of Nutritional Efforts on Discharged Elderly Patients

Herlev Hospital1 site in 1 country207 target enrollmentMay 1, 2018
ConditionsMalnutrition

Overview

Phase
N/A
Intervention
Not specified
Conditions
Malnutrition
Sponsor
Herlev Hospital
Enrollment
207
Locations
1
Primary Endpoint
Hospital readmissions
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
May 1, 2018
End Date
March 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jonas Anias Svendsen

Research Associate

Herlev Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients admitted to Oncology, Gastro-medical / Surgical, and Medical Department, HGH, Herlev.
  • At admission, found in nutritional risk score ≥3 according to NRS-
  • On special food concept, Herlev's Glories during hospitalization
  • Discharged to own home in a municipality in Planområde Midt (Ballerup, Herlev, Lyngby-Tårbæk, Gentofte, Gladsaxe, Rødovre, Egedal, Rudersdal, Furesø).
  • Can read, hear and understand Danish
  • Cognitive able to participate in the study, based on whether they are informed in time, place and own data.

Exclusion Criteria

  • Food allergy or intolerance
  • Planned weight loss or following a special diet
  • Receives enteral or parenteral nutrition
  • Patients with moderate to severe dysphagia, defined with a need for gratin or a creamy diet
  • Patients who does not want a food package or goodiebag
  • Patients who are permanently bedridden
  • Patients who are discharged to nursing homes or rehabilitation
  • Patients in isolation
  • Late palliative patients
  • Terminal patients

Outcomes

Primary Outcomes

Hospital readmissions

Time Frame: 6 months

Secondary Outcomes

  • Combined adverse advents(30 days, 16 weeks, 6 months)
  • Mortality(30 days, 16 weeks, 6 months)
  • Protein intake(16 weeks)
  • Physical function(16 weeks)
  • Energi Intake(16 weeks)
  • Appetite(16 weeks)
  • Weight(16 weeks)
  • Health related Quality of life(16 weeks)
  • Hospital readmissions(30 days, 16 weeks)

Study Sites (1)

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