Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
33 participants
INTERVENTIONAL
2015-04-18
2017-04-22
Brief Summary
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Methods: Randomized, unblinded, parallel design. The intervention group (IT) was nutritionally handled by the dietician, and the control group (C) by the nurses as previously with the possibility for dietetic help from the center.
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Detailed Description
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The primary endpoint was re-admission rate to hospital within 2 months.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Dietetic service
Nutritional assessment and therapy by dietitian throughout the hospital stay
Nutritional assessment and therapy
Nutritional screening, nutritional plan, follow-up and instructions on discharge
standard care
Nutritional handling by nurses supported by a dietician if needed
Standard care
Nutritional handling by nurse
Interventions
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Nutritional assessment and therapy
Nutritional screening, nutritional plan, follow-up and instructions on discharge
Standard care
Nutritional handling by nurse
Eligibility Criteria
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Inclusion Criteria
* acutely admitted to hospital
Exclusion Criteria
* unable to comply with the protocol
18 Years
ALL
No
Sponsors
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Jens Rikardt Andersen
OTHER
Responsible Party
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Jens Rikardt Andersen
Associate Professor
Principal Investigators
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Jens R Andersen
Role: PRINCIPAL_INVESTIGATOR
University of Copenhagen
Other Identifiers
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H-15004856
Identifier Type: -
Identifier Source: org_study_id
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