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Preventing Malnutrition and Restoring Nutritional Status in Hospitalized Children

Not Applicable
Completed
Conditions
Nutrition Disorders
Interventions
Procedure: Access to a Computerized Clinical Decision Support System (CCDDS)
Behavioral: Education of Healthcare workers
Other: Local assistance by a dietician
Registration Number
NCT01081587
Lead Sponsor
Hospices Civils de Lyon
Brief Summary

This cluster-randomized trial will evaluate the impact of a multifaceted intervention (including electronic medical alerts) coordinated by a Nutritional Support Team, on adherence to recommended practices for care of starved children, among health personnel of a large university hospital. A key component of the study is to assess whether improved adherence to guidelines leads to a reduction in rates of complications.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1457
Inclusion Criteria
  • medical and surgical units in a large teaching hospital providing pediatric acute care.
  • any hospital staff with direct patient care who are affiliated with a single unit (includes physicians, nurses, nursing assistants, physiotherapists, dieticians.
  • all children recorded as malnourished at their entrance in hospital
Exclusion Criteria
  • neonatal and intensive care units.
  • any hospital staff with direct patient care who are not affiliated with a single unit.
  • age under one month, liver or kidney abnormalities, severe heart failure, stay less than 2 days.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nutritional Support TeamAccess to a Computerized Clinical Decision Support System (CCDDS)-
Nutritional Support TeamEducation of Healthcare workers-
Nutritional Support TeamLocal assistance by a dietician-
Usual careAccess to a Computerized Clinical Decision Support System (CCDDS)-
Primary Outcome Measures
NameTimeMethod
Adherence to recommended practices (including weigh in, physiotherapy, nutrition survey and monitoring)At least 2 days depending on the hospitalisation time
Secondary Outcome Measures
NameTimeMethod
Incidence of complicationsAt least 2 days depending on the hospitalisation time
Nutritional status evolutionAt least 2 days depending on the hospitalisation time
Mean length and cost of stayAt least 2 days depending on the hospitalisation time
Appropriate call-in Nutritional Support TeamAt least 2 days depending on the hospitalisation time

Trial Locations

Locations (1)

Hospices Civils de Lyon (HCL) - Hôpital Femme-Mère-Enfant

🇫🇷

Bron, France

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